Trabajos medical device en OxfordCrear alertas

Responsibility for the care of adult patients undergoing investigation and treatment of heart rhythm conditions Day-to-day running of EP lab lists (patient consent and preparation, list coordination, discharge planning and administration) Support of ablation and cardiac implantable device lists Autonomous Fellow EP lists in the lab Presentation and discussion of clinical cases at the multi-professional MDT Participation in research, governance and clinical audit within the unit. Arrhythmia Clinic at OUH and occasionally associated hospitals. Involvement in the training and supervision of junior medical staff in the EP lab, including the teaching of medical and nursing students. Oxford University Hospitals NHS Foundation Trust #J-18808-Ljbffr

OrganOx is a commercial stage organ technology company dedicated to developing technologies to improve outcomes for patients with acute or chronic organ failure. The company was established as a spin out of the University of Oxford in 2008 and is now part of the Terumo Group. OrganOx is a pioneer in normothermic machine perfusion (NMP). It's flagship platform, the metra®, is available for use in the U.S., Europe, Canada, and Australia. It has been utilized in over 7,000 liver transplants to date to keep donor livers in a metabolically active state outside the body enabling longer preservation times and functional assessment of the organ prior to transplant, leading to an increased number of organs available for transplant. Founded in 1921, Terumo Corporation (TSE:4543) strives to fulfil its mission of "Contributing to Society through Healthcare" by providing a comprehensive range of solutions in the fields of therapeutic procedures, hospital operations, and life sciences in more than 160 countries and regions. OrganOx is a commercial stage organ technology company dedicated to developing technologies to improve outcomes for patients with acute or chronic organ failure. The company was established as a spin out of the University of Oxford in 2008 and is now part of the Terumo Group. OrganOx is a pioneer in normothermic machine perfusion (NMP). It's flagship platform, the metra®, is available for use in the U.S., Europe, Canada, and Australia. It has been utilized in over 7,000 liver transplants to date to keep donor livers in a metabolically active state outside the body enabling longer preservation times and functional assessment of the organ prior to transplant, leading to an increased number of organs available for transplant. Founded in 1921, Terumo Corporation (TSE:4543) strives to fulfil its mission of "Contributing to Society through Healthcare" by providing a comprehensive range of solutions in the fields of therapeutic procedures, hospital operations, and life sciences in more than 160 countries and regions. The Software Quality Engineer will work closely with R&D, Engineering, Post‑Market Operations and Quality teams to ensure effective control of design, development, risk assessment, and change control. They will provide Quality and Design Assurance oversight across the software lifecycle for medical devices, including IEC 62304 software and digital health applications. The role works closely with Regulatory Affairs to ensure software documentation and procedures meet applicable standards and regulatory expectations. Building upon the company's success in organ preservation for liver transplantation, several new applications of the technology are now being actively developed. The successful candidate will join a rapidly growing Quality department working with R&D, Post-Market Engineering, Cybersecurity and Regulatory Affairs and play a key role in supporting compliance with EU MDR, FDA requirements and applicable software and cybersecurity standards, for new and existing products. A central responsibility of the role is ensuring effective software risk management, particularly the development and maintenance of Software FMEAs (SFMEAs), software hazard analyses, cybersecurity risk assessments and associated risk controls. This is an onsite role in Oxford with flexibility. • Assure software quality throughout the full lifecycle process in accordance with OrganOx software standards and procedures for software up to safety class C per IEC 62304., • Ensure effective implementation of software design controls, including requirements, architecture, verification and validation, configuration management, change control and release management., • Ensure appropriate traceability between software hazards, failure modes, software requirements, risk-control measures and verification evidence., • EnsuresoftwareFMEAs are aligned with system-level risk analyses, including system FMEAs, use-related risk analyses and the overall ISO 14971 risk-management file., • Review software lifecycle documentation for completeness, consistency, traceability and regulatory compliance., • Participate in design reviews, risk reviews, change assessments, project milestones and release-readiness reviews., • Provide Quality oversight of cybersecurity risk management, including threat modelling, vulnerability assessment, SOUP and third-party software., • Maintain and improve software procedures in line with IEC 62304, ISO 13485, ISO 14971, EU MDR, applicable FDA requirements and cybersecurity guidance., • Supporting Quality oversight of computer system validation/assurance (CSV)/CSA., • Ensure software defects, complaints, post-market information and cybersecurity vulnerabilities are assessed for their impact on the SFMEA and wider risk-management file., • Support software-related nonconformances, CAPAs, complaints, audits and regulatory inspections., • Contribute as part of the team to assist in other tasks as necessary., • Adhereto the letter and spirit ofOrganOx'sCode of Conduct and all other company policies, • Experience as a software quality engineer, or in a similar quality role, within the medical device industry, supporting SaMD, digital health applications or software in a medical device., • Experience developing, facilitating and reviewing SFMEAs and software hazard analyses for medical-device softwareunderISO 14971., • Experience reviewing software requirements, architecture, traceability, verification evidence, changes and release documentation., • Experience working in cybersecurity risk assessment (Desirable)., • Experienceinsupporting, conducting, and reviewing activities and processes related to computer system validation (CSV)., • Experience with GAMP5 classification used for CSV (Desirable)., • Practical working knowledge of IEC 62304, ISO 14971, ISO 13485, EU MDR and applicable FDA software requirements and guidance., • Strong analytical and communication skills, with the ability to facilitate cross-functional risk discussions and constructively challenge technical decisions., • Experience working within a quality management system and following standard operating procedures., • Experience working in Quality within the medical device industry (Desirable)., • Experience with SOUP, nonconformances,CAPA, complaints and regulatory audits (Desirable)., • Knowledge of IEC 81001-5-1, IEC 82304-1 and FDA cybersecurity guidance (Desirable), • A degree or equivalent experience in software engineering, computer science, information engineering, systems engineering, quality engineering or a related discipline. At OrganOx, we value innovation, evidence, integrity, teamwork, respect, and passion. We offer competitive compensation and comprehensive benefits, including healthcare and retirement plans. We support work-life balance and provide opportunities for ongoing professional development. We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to age, disability, gender reassignment, marriage and civil partnership, pregnancy and maternity, race, religion or belief, sex, sexual orientation race, or any other characteristics protected by law. #J-18808-Ljbffr

Main area Electrophysiology (EP) Grade NHS Medical & Dental: Senior Clinical Fellow Contract Permanent: N/a Hours Full time - 40 hours per week (N/a) Job ref 321-MRC-MS-8271100-S6 Employer Oxford University Hospitals NHS Foundation Trust Employer type NHS Site Oxford University Foundation Trust Town Headington Salary £67,325 - £76,582 Per Annum Salary period Yearly Closing 16/11/2026 23:59 Oxford University Hospitals NHS Foundation Trust is one of the largest NHS teaching trusts in the country. It provides a wide range of general and specialist clinical services and is a base for medical education, training and research. The Trust comprises of four hospitals - the John Radcliffe Hospital, Churchill Hospital and Nuffield Orthopaedic Centre in Headington and the Horton General Hospital in Banbury. Our values, standards and behaviours define the quality of clinical care we offer and the professional relationships we make with our patients, colleagues and the wider community. We call thisDelivering Compassionate Excellenceand its focus is on our values of compassion, respect, learning, delivery, improvement and excellence. Many of our recruitment programmes useValue Based Interviewingto identify those who have the skills we seek, who share our values and who are able to deliver compassionate excellence from the outset. We know that this makes a significant difference to your job satisfaction and above all the outcomes and experience of our patients and their families. For more information about our Values and Value Based Interviewing please visit www.ouh.nhs.uk/about/vision-and-values This post is aimed at senior trainees in cardiac electrophysiology who already have experience in catheter ablation and cardiac device implantation who are within 6 months of their CCT. The job is primarily EP Lab-based with one clinic per week (and occasional extras) and specialist EP ward referral duties. The aim is to gain experience in complex ablation (e.g. atrial fibrillation, ventricular tachycardia), developing competence as a solo operator and prepare for a consultant role. • Responsibility for the care of adult patients undergoing investigation and treatment of heart rhythm conditions, • Day-to-day running of EP lab lists (patient consent and preparation, list coordination, discharge planning and administration), • Support of ablation and cardiac implantable device lists, • Autonomous “Fellow” EP lists in the lab, • Presentation and discussion of clinical cases at the multi-professional MDT, • Participation in research, governance and clinical audit within the unit., • Arrhythmia Clinic at OUH and occasionally associated hospitals., • Involvement in the training and supervision of junior medical staff in the EP lab, including the teaching of medical and nursing students. Oxford University Hospitals NHS Foundation Trust is one of the largest NHS teaching trusts in the country. It provides a wide range of general and specialist clinical services and is a base for medical education, training and research.The Trust comprises four hospitals - the John Radcliffe Hospital, Churchill Hospital and Nuffield Orthopaedic Centre in Headington and the Horton General Hospital in Banbury. Our values, standards and behaviours define the quality of clinical care we offer and the professional relationships we make with our patients, colleagues and the wider community. We call this Delivering Compassionate Excellence and its focus is on our values of compassion, respect, learning, delivery, improvement and excellence. These values put patients at the heart of what we do and underpin the quality healthcare we would like for ourselves or a member of our family. Watch how we set out to deliver compassionate excellence via the OUH YouTube channel . • Responsibility for the care of adult patients undergoing investigation and treatment of heart rhythm conditions, • Day-to-day running of EP lab lists (patient consent and preparation, list coordination, discharge planning and administration), • Support of ablation and cardiac implantable device lists, • Autonomous “Fellow” EP lists in the lab, • Presentation and discussion of clinical cases at the multi-professional MDT, • Participation in research, governance and clinical audit within the unit., • Arrhythmia Clinic at OUH and occasionally associated hospitals., • Involvement in the training and supervision of junior medical staff in the EP lab, including the teaching of medical and nursing students., • GMC Full Licence to Practice, • MRCP or equivalent, • General training in cardiology to registrar year 5 level or equivalent., • Experience in cardiac electrophysiology (a minimum of 12 months, • Within 6 months of CCT in Cardiology, • Experience in transseptal punctures (solo operator). Previous first-operatorexperience in pulmonary vein isolation ablation. Interest in research withpublications. CCT in Cardiology and Cardiac Electrophysiology, • experience in pulmonary vein isolation ablation. Interest in research withpublications., • experience in pulmonary vein isolation ablation. Interest in research withpublications. Sexual Safety Charter : In 2023NHS England launched its first sexual safety charter, and our Trust proudly signed it. We pledge zero tolerance for inappropriate sexual behaviour and commit tothe ten core principles Oxford University Hospitals promotes a safe, respectful hiring environment. Vacancy Closures: Please note, this vacancy may close early if a high volume of applications are received. Visa and Immigration: Oxford University Hospitals NHS Foundation Trust is able to offer Certificates of Sponsorship for all eligible roles for a Skilled Worker Visa without exception, provided the role meets the minimum salary and skill level criteria set by the Home Office (UKVI). All eligible candidates will be considered with equal consideration at all stages of the application and recruitment process. Skilled worker: Health and Care Visa | NHS Employers / Work in the UK - GOV.UK COVID-19: The COVID-19 vaccination remains the best way to protect yourself, your family, your colleagues and of course our patients from the virus when working in our healthcare settings. Whilst COVID-19 vaccination is not a condition of employment, we do encourage our staff to get vaccinated. If you are unvaccinated there is helpful advice and information at Oxfordshire County Council Website where you can also find out more about how to access vaccination. Probation Period: This post is subject to a 6 month probationary period. If you currently hold a contract of employment with the Oxford University Hospitals, this will not apply. This statement does not apply to Medical staff or Executive Appointments. Referencing: When providing employment reference details please provide correct work related email addresses so references can be sought promptly when we are looking to progress your application. Your first referee will need to be your line manager, supervisor or clinical lead from your current or most recent post or place of study. Please note that if you have previously worked for the Trust we will require a reference from your last Manager, this information is essential if your offer of employment is to be confirmed. To note: Applicants must write their own applications. If AI tools are used, the application may be rejected as this document is crucial for assessment. This does not prevent you from seeking support via AI with applications for the purposes of any disability and/or long-term health conditions. When using AI to help write your application, it is important to personalise it, especially your supporting statement. While AI can simplify the process, it will not fully understand the job's requirements and/or be able to showcase your skills, knowledge, and experience. Write your statement to show why you are interested in the role and how you would be a valued member of the team/OUH employee. No unsolicited recruitment agency telephone calls or emails. You must have appropriate UK professional registration. This post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service. Please note that this job advertisement will close automatically once the application limit is reached, regardless of whether this occurs before the advertised closing date. #J-18808-Ljbffr

IonQ, Inc. [NYSE: IONQ] is the world’s leading quantum platform and merchant supplier — delivering integrated quantum solutions across computing, networking, sensing, and security. IonQ’s newest generation of quantum computers, the IonQ Tempo, is the latest in a line of cutting‑edge systems that have been helping customers and partners including Amazon Web Services, and AstraZeneca achieve 20x performance results and accelerate innovation in drug discovery, materials science, financial modeling, logistics, cybersecurity, and defense. In 2025, the company achieved 99.99% two‑qubit gate fidelity, setting a world record in quantum computing performance. Headquartered in College Park, Maryland, IonQ has operations in California, Colorado, Massachusetts, Tennessee, Washington, Italy, South Korea, Sweden, Switzerland, Canada, and the United Kingdom. Our quantum computing services are available through all major cloud providers, while we also meet the needs of networking and sensing customers across land, sea, air, and space. IonQ is making quantum platforms more accessible and impactful than ever before. Oxford, UK Hybrid Quantum is now, and it's built here. Oxford Ionics, now part of IonQ, is pioneering the next generation of quantum computing. Using our world‑leading trapped‑ion technology, we’re building the most powerful, accurate and reliable quantum systems to tackle problems that today's supercomputers cannot solve. We’re looking for an enthusiastic and highly technical Software Engineer for our Non‑Realtime Controllers team who will thrive in our dynamic cross‑disciplinary environment. In this role, you will be responsible forworking closely with our software engineers, our systems team, and our quantum scientists to build and operate the software that controls the hardware surrounding our quantum computers, contributing to the team’s mission of enabling our systems team to operate the physical quantum computers and our science teams to experiment building towards fault tolerant computation. Previous exposure to quantum systems is not required. You’ll play an important part in shaping the non‑realtime controllers, the system operations and services that support our work in building the world’s most advanced quantum systems. In this position, you will work hands‑on with hardware control end to end, from the device protocol up to a service running reliably across our fleet, supporting the effective delivery of non‑realtime controllers that ensure that the critical supporting hardware of a quantum computer is observable, controllable and reliable (from cryogenic compressors to lasers, wavemeters, and various sensors). You’ll have the opportunity to own areas of the hardware control surface end to end, from the device protocol up to a service running reliably across our fleet, contributing directly to the success of building utility‑scale quantum computers. • Own a group of device controllers end to end, covering API design, implementation, rollout and ongoing operational health, • Make services robust against the ways real instruments fail and strengthen observability, health checking and alerting, • Bring devices onto our current framework, and roll the result out across the fleet without disrupting running experiments, • Work closely with the software. systems and science teams who depend on these services, and to ensure our work integrates seamlessly with the wider software architecture To be successful, you will need strong programming skills in a systems programming language and hands‑on experience interfacing with hardware, and a track record of making software behave well against unreliable external dependencies. We’re looking for someone who can quickly iterate on low-level code in a collaborative, cross‑disciplinary, environment and contribute effectively within a fast moving, highly technical team. • Strong programming skills in one or more systems programming languages and the appetite to work in a Rust codebase, • Experience with some hardware instrument and communication protocols (e.g. SCPI, serial, TCP/IP, USB, or similar), • Comfortable owning the production behaviour of what you build, not just its correctness in test, • Excellent communication skills both within software and across disciplines, and an interest in helping other engineers get better at the craft without wanting to stop building yourself Be part of a team that’s shaping the future of quantum. We offer more than just a role, you’ll join a world class community of scientists, engineers and innovators working to unlock the full potential of quantum computing. We offer a range of benefits, including opportunities to further your career alongside industry leaders, a competitive salary with IonQ stock options, an annual performance bonus, generous annual leave, flexible hybrid working, private medical and dental insurance for you and your family, and much more. Join us and be part of the future of quantum computing. We’re proud to be an equal opportunity employer and welcome applicants from all backgrounds. Compensation will vary based on individual factors such as education, qualifications, and experience of the final candidate(s), specific office location, and calibration against relevant market data and internal team equity. Posted base salary figures are subject to change as new market data becomes available. Our benefits include comprehensive medical, dental, and vision plans, matching 401(k), unlimited PTO and paid holidays, parental/adoption leave, legal insurance, and a home technology stipend. Details of participation in these benefit plans will be provided when a candidate receives an offer of employment. At IonQ, we believe in fair treatment, access, opportunity, and advancement for all while striving to identify and eliminate barriers. We empower employees to thrive by fostering a culture of autonomy, productivity, and respect. We are dedicated to creating an environment where individuals can feel welcomed, respected, supported, and valued. We are committed to equity and justice. We welcome different voices and viewpoints and do not discriminate on the basis of race, religion, ancestry, physical and/or mental disability, medical condition, genetic information, marital status, sex, gender, gender identity, gender expression, transgender status, age, sexual orientation, military or veteran status, or any other basis protected by law. We are proud to be an Equal Employment Opportunity employer. The position you are applying for will require access to technology that is subject to U.S. export control and government contract restrictions. Employment with IonQ is contingent on either verifying “U.S. Person” (e.g., U.S. citizen, U.S. national, U.S. permanent resident, or lawfully admitted into the U.S. as a refugee or granted asylum) status for export controls and government contracts work, obtaining any necessary license, and/or confirming the availability of a license exception under U.S. export controls. Please note that in the absence of confirming you are a U.S. Person for export control and government contracts work purposes, IonQ may choose not to apply for a license or decline to use a license exception (if available) for you to access export‑controlled technology that may require authorization, and similarly, you may not qualify for government contracts work that requires U.S. Persons, and IonQ may decline to proceed with your application on those bases alone. Accordingly, we will have some additional questions regarding your immigration status that will be used for export control and compliance purposes, and the answers will be reviewed by compliance personnel to ensure compliance with federal law. Due to applicable export control laws and regulations, candidates must be a U.S. citizen or national, U.S. permanent resident (i.e., current Green Card holder), or lawfully admitted into the U.S. as a refugee or granted asylum. Accordingly, we will have some additional questions regarding your immigration status that will be used for export control and compliance purposes, and the answers will be reviewed by compliance personnel to ensure compliance with federal law. #J-18808-Ljbffr

OrganOx is a commercial stage organ technology company dedicated to developing technologies to improve outcomes for patients with acute or chronic organ failure. The company was established as a spin out of the University of Oxford in 2008 and is now part of the Terumo Group. OrganOx is a pioneer in normothermic machine perfusion (NMP). It's flagship platform, the metra®, is available for use in the U.S., Europe, Canada, and Australia. It has been utilized in over 7,000 liver transplants to date to keep donor livers in a metabolically active state outside the body enabling longer preservation times and functional assessment of the organ prior to transplant, leading to an increased number of organs available for transplant. Founded in 1921, Terumo Corporation (TSE:4543) strives to fulfil its mission of “Contributing to Society through Healthcare” by providing a comprehensive range of solutions in the fields of therapeutic procedures, hospital operations, and life sciences in more than 160 countries and regions. The Senior Digital Infrastructure & DevOps Engineer will be responsible for designing, building, securing, automating and maintaining the cloud infrastructure and the deployment foundations that support OrganOx’s digital products and connected device services. The role is primarily Digitalfocused, supporting software engineering teams with scalable environments, infrastructure-as-code, CI/CD, observability, cybersecurity and reliable operational practices for regulated medical device software. The role will also provide infrastructure and engineering support to the Data domain where shared platforms, cloud services, integration pipelines, Azure resources, SAP interfaces, Databricks environments, or high-throughput device and enterprise data flows require robust engineering input. The successful candidate will act as a practical bridge between Digital and Data, while retaining primary accountability for the Digital infrastructure, DevOps and cloud engineering responsibilities. This is a hands‑on senior role suited to someone who is comfortable working across cloud infrastructure, software delivery, automation, security, operational support, regulated digital product development and selective data-platform engineering. This is an office based role in Oxford, with flexibility, to ensure stakeholder engagement with Engineering, Quality and other relevant business units. Listed below are the major responsibilities of the role and a brief description of some of the key tasks to be performed. This list is not totally exhaustive. • Design, build, secure, and maintain scalable Azure cloud infrastructure for OrganOx digital products, connected device services, development environments, and production deployments., • Own and improve core platform capabilities across networking, identity and access management, storage, compute, monitoring, backup, resilience, security, and cost control., • Implement repeatable infrastructure-as-code, CI/CD, automated deployment, testing, release controls, and operational handover practices using appropriate tooling., • Work closely with software engineering teams and development partners to support development, integration, validation, deployment, troubleshooting, and ongoing platform support., • Establish monitoring, logging, alerting, observability, and incident-support practices to improve reliability, performance, supportability, and operational readiness., • Ensure infrastructure and delivery practices support cybersecurity, data protection, access control, encryption, auditability, and compliance expectations for regulated healthcare software., • Provide infrastructure and engineering input for shared Digital/Data platforms, including connected device cloud services, Azure resources, Databricks, SAP interfaces, data pipelines, and enterprise data flows where required., • Mentor less experienced engineers, contribute to technical standards, and maintain appropriate architecture, deployment, runbook, support, and regulated lifecycle documentation., • Adhere to the letter and spirit of OrganOx’s Code of Conduct and all other company policies, • Proven experience in infrastructure, DevOps, cloud engineering, platform engineering, or software delivery, ideally within regulated healthcare, life sciences, or medical technology (essential), • Strong hands‑on Microsoft Azure experience across networking, identity and access management, storage, compute, Key Vault, monitoring, resource management, resilience, security, and cost management (essential), • Experience with infrastructure-as-code, CI/CD, environment management, automated deployment, testing, release controls, and operational support using tools such as Terraform, Bicep, Azure DevOps, or GitHub Actions (essential), • Strong scripting, automation, troubleshooting, observability, logging, alerting, incident diagnosis, and performance improvement skills (essential), • Good understanding of cybersecurity, secure configuration, access control, encryption, secrets management, auditability, and compliance expectations for regulated software systems (essential), • Ability to support software teams and development partners through development, integration, deployment, operational handover, and ongoing platform support (essential), • Working knowledge of data‑platform infrastructure concepts, including Azure data services, Databricks, SAP integration, ETL/ELT pipelines, orchestration and data governance sufficient to support shared Digital/Data needs (essential), • Strong communication, stakeholder‑management, technical leadership and mentoring skills across technical and non-technical teams (essential), • Experience with IEC 62304, ISO 14971, or other regulated software development and risk‑management processes (desirable), • Experience with connected medical device platforms, cloud‑hosted digital health services, remote monitoring, or high‑throughput device data services (desirable), • Experience with containerisation, Kubernetes, AKS, API management, application gateways, or equivalent cloud application hosting technologies (desirable), • Experience with Databricks, Spark, Delta Lake, Unity Catalog, Azure Data Factory, SAP BW/4HANA, S/4HANA, OData, CDS views, CDC patterns, or equivalent enterprise data technologies (desirable), • Microsoft Azure certifications such as AZ-104, AZ-305, AZ-400, equivalent practical experience, or familiarity with cloud cost optimisation and FinOps practices (desirable), • Degree in Computer Science, Engineering, or equivalent technical qualification. At OrganOx, we value innovation, evidence, integrity, teamwork, respect, and passion. • We offer competitive compensation and comprehensive benefits, including healthcare and retirement plans., • We support work-life balance., • We provide opportunities for ongoing professional development. We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to age, disability, gender reassignment, marriage and civil partnership, pregnancy and maternity, race, religion or belief, sex, sexual orientation race, or any other characteristics protected by law. #J-18808-Ljbffr

Cardiac Cath Lab/Cardiology Nurse (Bank) Oxford Manor Hospital | Nursing | Bank | Part time Up to £35.00 depending on experience The department opening hours are between 8-6 Monday to Friday and some Saturday working Working on the bank means you are not contracted to a set number of hours per week but instead work on an ad-hoc basis to suit the needs of the business and your availability. The intervention suite completes a range of procedures including; cardiac device implantation such as Pacemakers, CRT, ICDs and cardioversion in addition to Radiology interventional procedures. As well as scrubbing and circulating for cases, you will be involved in the patient journey from start to finish, including pre-assessment outpatient work, patient follow up and supporting wards and recovery with your expertise. You’ll also work with a range of consultants whilst developing your own skills in the cardiology environment. • Providing a specialist private cardiac service to patients requiring cardiac device implantation and cardioversion., • Being involved in the whole patient journey from pre-assessment to discharge ensuring patients individual needs are met and planned accordingly., • Acting as scrub nurse to Consultant Cardiologists and promote and maintain a caring and highly professional standard of nursing, meeting the needs of the patients undergoing Cath Lab procedures., • Working with the cardiology ward/recovery staff ensuring patients are admitted and prepared for Cath Lab procedures ensuring appropriate investigations are done and accurately recording documentation., • To be an RN with post registration experience., • Experience of working in a Cardiac Catheter lab environment., • Initiative to manage your own clinical workload within a small team We want you to love coming to work, feeling healthy, happy and valued. That’s why we’ve developed a benefits package with you in mind. This includes holiday in line with the working time directive, access to our pension scheme and discounted gym membership at £35.00 a month. Our modern hospital is based within a stone’s throw of the historic City of Oxford, a world-renowned centre of excellence for surgical and medical expertise. We are proud of the wonderful environment and team we have established, providing our patients with first class care. We operate 6 well equipped and modern operating theatres with 64 well-presented ensuite rooms. We cater for inpatient and day care, providing a broad range of surgical specialties and clinics including Paediatrics, Oncology, Interventional Cardiology & Radiology, Orthopaedics, Endoscopy, Gynaecology, Urology, Ophthalmology as well as women’s and men’s health clinics. The hospital is located with excellent transport links by road and rail, both to and from London, Thames Valley, and the Midlands. It starts with you. #J-18808-Ljbffr

At the Ellison Institute of Technology (EIT), we're on a mission to translate scientific discovery into real world impact. We bring together visionary scientists, technologists, engineers, researchers, educators and innovators to tackle humanity's greatest challenges in four transformative areas: • Health, Medical Science & Generative Biology, • Food Security & Sustainable Agriculture, • Climate Change & Managing CO₂, • Artificial Intelligence & Robotics This is ambitious work - work that demands curiosity, courage, and a relentless drive to make a difference. At EIT, you'll join a community built on excellence, innovation, tenacity, trust, and collaboration, where bold ideas become real-world breakthroughs. Together, we push boundaries, embrace complexity, and create solutions to scale ideas from lab to society. Explore more at . Within this ecosystem, the Pathogen Mission exemplifies EIT's commitment to transformative science. It aims to revolutionise the diagnosis and treatment of infectious diseases by leveraging whole genome sequencing (WGS)-based metagenomic and pathogen-specific analytical tools. This remit includes the development of a decentralised, sample-to-answer sequencing diagnostic platform for infectious diseases, enabling rapid and accurate analysis of patient samples without prior assumptions. Supported by Oracle Inc.'s cloud-computing scale and security infrastructure, the Pathogen Mission is progressing towards certified diagnostic products for deployment in laboratories, hospitals, and public health organisations worldwide. We're seeking an experienced and innovative Senior MEMS Development Engineer to develop novel microfabricated devices and sensor interfaces for next-generation nanopore sequencing technologies. This hands‑on role will focus on designing, prototyping, and characterising MEMS devices, taking concepts from proof‑of‑concept through to integrated multi‑channel sensing systems. Working closely with a Senior Electronics R&D Engineer, you'll drive device development through iterative design, testing, and optimisation. You’ll tackle challenges spanning microfabrication, materials, device architecture, and MEMS-electronics integration while collaborating with external fabrication partners and technical suppliers. As the programme grows, you’ll help establish the MEMS engineering capabilities, processes, and technical foundations needed to support a wider multidisciplinary team. • Take technical ownership of the MEMS engineering development of novel microfabricated sensing structures and device interfaces, from early concepts through to functional prototypes and integrated systems, • Design and develop microfabricated devices and test structures, including the selection of materials, fabrication processes and device geometries, • Develop and evaluate fabrication approaches using established semiconductor and MEMS manufacturing techniques, adapting processes to meet the requirements of novel sensing devices, • Work closely with the Senior Electrical R&D Engineer to co‑develop and evaluate prototype devices, using experimental findings to guide iterative improvements in MEMS design and electronic integration, • Design and characterise mechanical, electrical and material interfaces, investigating their influence on device performance, reliability and repeatability, • Develop experimental methods and test structures to assess fabrication quality, dimensional accuracy, device performance and reliability, • Investigate the effects of materials, surface properties, fabrication tolerances and assembly processes on device behaviour and performance, • Collaborate with electrical and mechanical engineers to develop prototype assemblies, alignment methods and experimental test platforms, • Identify and resolve fabrication challenges through design iteration, experimental characterisation and failure analysis, • Develop increasingly sophisticated prototype devices as the project progresses, supporting the transition from initial feasibility studies to integrated nanopore sensing systems, • Identify and engage specialist external fabrication facilities, engineering suppliers and technical collaborators to support the development and manufacture of prototype components and devices, • Define technical specifications and fabrication requirements for external suppliers, including design documentation, material requirements, dimensional tolerances and performance criteria, • Coordinate technical activities with external suppliers and collaborators, reviewing fabrication approaches, monitoring progress and evaluating deliverables against agreed requirements, • Plan and execute structured experiments, analyse performance data and translate findings into engineering requirements and design improvements, • Contribute to the selection and development of fabrication methods, considering manufacturability, scalability, cost and process reliability, • Maintain clear technical documentation, design records and experimental results, contributing to intellectual property development and technical reviews while ensuring appropriate confidentiality, • Provide technical guidance and mentoring as the engineering team expands, helping establish robust engineering practices and development processes We welcome applicants from industry, applied research and academia who can demonstrate strong technical expertise and practical engineering capability. • Degree in Electrical Engineering, Mechanical Engineering, Materials Science, Physics or a related discipline, or equivalent relevant experience, • Significant experience in MEMS engineering, semiconductor microfabrication or microdevice development, ideally involving novel sensors, electronic interfaces or precision microfabricated systems, • Strong understanding of MEMS design principles, materials selection and microfabrication techniques, • Experience designing microfabricated devices using CAD tools, including the preparation of layouts, fabrication drawings or photolithography mask designs, • Practical knowledge of semiconductor and MEMS manufacturing processes, such as photolithography, thin‑film deposition, etching, surface treatment and metallisation, • Experience developing and characterising prototype devices, including dimensional, mechanical and electrical evaluation, • Ability to understand and resolve fabrication challenges through experimental investigation, design modification and process optimisation, • Knowledge of material properties, fabrication tolerances and their influence on device functionality and reliability, • Experience planning and executing structured experimental programmes to characterise complex devices and resolve technical challenges, • Ability to work independently, establish technical approaches and deliver functional prototypes in an early‑stage R&D environment, • Experience collaborating with multidisciplinary teams and translating requirements between MEMS, electronics, mechanical engineering and device fabrication, • Ability to develop clear technical specifications and work effectively with external fabrication facilities, engineering suppliers or development partners, • Experience developing MEMS or microfabricated devices for biosensing, electrochemical sensing, nanopore technologies or other sensor applications, • Knowledge of silicon micromachining, wafer processing and microelectronic device fabrication, • Experience with microfabricated electrodes, conductive thin films, dielectric materials or electronic sensor interfaces, • Familiarity with microelectronic packaging, device assembly, bonding and integration of MEMS with electronic systems, • Experience with polymeric materials, elastomeric components or other compliant materials used in microsystems, • Knowledge of mechanical contact behaviour, surface interactions, material deformation and reliability testing at small length scales, • Experience with optical microscopy, electron microscopy, profilometry, surface analysis or other microdevice characterisation techniques, • Experience designing devices that incorporate fluidic, electrochemical or biological components, • Familiarity with finite element analysis or other simulation methods for mechanical, thermal or material behaviour, • Experience working with external MEMS foundries, academic cleanroom facilities or specialist microfabrication suppliers, • Knowledge of fabrication process development, process yield improvement and quality control, • Understanding of design for manufacture, engineering reliability and transitioning prototype devices towards scalable production, • Hands‑on and inventive: Enjoys solving technical challenges through practical engineering, experimentation and rapid prototyping, • Comfortable with early‑stage R&D: Able to work effectively where solutions are not yet established and technical requirements evolve through experimentation, • Analytical and systematic: Uses sound engineering judgement and quantitative evidence to understand complex behaviour and guide design decisions, • Collaborative: Works closely with specialists in electronics, mechanical engineering, chemistry and MEMS fabrication, as well as external technical partners, to develop integrated solutions, • Independent and proactive: Can establish experimental capabilities, identify priorities and progress technical work with limited existing infrastructure, • Technically ambitious: Motivated by challenging engineering problems and developing technologies with the potential for substantial real‑world impact, • Clear communicator: Able to explain complex technical challenges, document findings and communicate requirements effectively with colleagues, suppliers and external collaborators, • Salary: Competitive + travel allowance + bonus, • Enhanced holiday pay, • Pension, • Life Assurance, • Income Protection, • Private Medical Insurance, • Hospital Cash Plan, • Therapy Services, • Perk Box, • Electric Car Scheme, • You must have the right to work permanently in the UK with a willingness to travel as necessary. In certain cases, we can consider sponsorship, and this will be assessed on a case‑by‑case basis, • You will live in, or within easy commuting distance of, Oxford (or be willing to relocate), • You must be eligible to work in the UK with occasional travel (1-3 trips per year) #J-18808-Ljbffr

This post is aimed at senior trainees in cardiac electrophysiology who already have experience in catheter ablation and cardiac device implantation who are within 6 months of their CCT. The job is primarily EP Lab-based with one clinic per week (and occasional extras) and specialist EP ward referral duties. The aim is to gain experience in complex ablation (e.g. atrial fibrillation, ventricular tachycardia), developing competence as a solo operator and prepare for a consultant role. • Responsibility for the care of adult patients undergoing investigation and treatment of heart rhythm conditions, • Day-to-day running of EP lab lists (patient consent and preparation, list coordination, discharge planning and administration), • Support of ablation and cardiac implantable device lists, • Autonomous Fellow EP lists in the lab, • Presentation and discussion of clinical cases at the multi-professional MDT, • Participation in research, governance and clinical audit within the unit., • Arrhythmia Clinic at OUH and occasionally associated hospitals., • Involvement in the training and supervision of junior medical staff in the EP lab, including the teaching of medical and nursing students. Oxford University Hospitals NHS Foundation Trust is one of the largest NHS teaching trusts in the country. It provides a wide range of general and specialist clinical services and is a base for medical education, training and research. The Trust comprises four hospitals - the John Radcliffe Hospital, Churchill Hospital and Nuffield Orthopaedic Centre in Headington and the Horton General Hospital in Banbury. Our values, standards and behaviours define the quality of clinical care we offer and the professional relationships we make with our patients, colleagues and the wider community. We call this Delivering Compassionate Excellence and its focus is on our values of compassion, respect, learning, delivery, improvement and excellence. These values put patients at the heart of what we do and underpin the quality healthcare we would like for ourselves or a member of our family. Watch how we set out to deliver compassionate excellence via the OUH YouTube channel. • Responsibility for the care of adult patients undergoing investigation and treatment of heart rhythm conditions, • Day-to-day running of EP lab lists (patient consent and preparation, list coordination, discharge planning and administration), • Support of ablation and cardiac implantable device lists, • Autonomous Fellow EP lists in the lab, • Presentation and discussion of clinical cases at the multi-professional MDT, • Participation in research, governance and clinical audit within the unit., • Arrhythmia Clinic at OUH and occasionally associated hospitals., • Involvement in the training and supervision of junior medical staff in the EP lab, including the teaching of medical and nursing students., • GMC Full Licence to Practise, • MRCP or equivalent, • General training in cardiology to registrar year 5 level or equivalent., • Experience in cardiac electrophysiology (a minimum of 12 months, • Within 6 months of CCT in Cardiology, • Experience in transseptal punctures (solo operator). Previous first-operator experience in pulmonary vein isolation ablation. Interest in research with publications. CCT in Cardiology and Cardiac Electrophysiology, • experience in pulmonary vein isolation ablation. Interest in research with publications., • experience in pulmonary vein isolation ablation. Interest in research with publications. 321-MRC-MS-8271100-S6 #J-18808-Ljbffr

• Bonus Scheme, • 25 Days Holiday + Bank Holidays, • Life Assurance, • Income Protection, • Enhanced Sick Pay We are supporting a leading engineering and manufacturing organisation in the search for a to join a growing team supporting complex, high-value programmes within a highly regulated environment. This is an excellent opportunity for an engineer who enjoys driving process improvement, supporting new product introduction and implementing robust manufacturing solutions from concept through to production. Working closely with engineering, quality, operations and project teams, you will play a key role in improving manufacturing capability, reducing waste and ensuring products are delivered safely, efficiently and to the highest quality standards. As a Manufacturing / Process Engineer, you will be responsible for developing and improving manufacturing processes, supporting production readiness and driving continuous improvement across the operation. You will work on both existing and new products, ensuring manufacturing methods, tooling, documentation and process controls are robust, efficient and capable of meeting customer requirements. • Develop and improve manufacturing processes across production operations, • Support NPI projects from concept through to full production release, • Create and maintain manufacturing documentation, SOPs and work instructions, • Lead process validation and manufacturing readiness activities, • Identify and implement process improvements to increase efficiency and reduce waste, • Conduct root cause investigations and implement corrective actions, • Analyse production data and KPIs to drive operational improvements, • Support equipment, tooling and fixture improvement projects, • Work closely with quality, engineering and production teams to achieve programme objectives, • Drive Lean Manufacturing and Continuous Improvement initiatives across the site We are interested in speaking with candidates from manufacturing, production, process or industrial engineering backgrounds. • Experience within a Manufacturing Engineer, Process Engineer, Production Engineer or similar role, • Strong background in manufacturing process improvement, • Experience supporting NPI and production launches, • Knowledge of Lean Manufacturing, Six Sigma or Continuous Improvement methodologies, • Experience with process validation, SOP creation and process documentation, • Strong problem-solving and root cause analysis skills, • Ability to work effectively with cross-functional teams, • Experience within aerospace, nuclear, automotive, medical device or other advanced manufacturing environments would be advantageous, • Full right to work in the UK without restrictions, • Opportunity to influence manufacturing strategy and process performance, • Work on technically challenging engineering programmes, • Significant project ownership and stakeholder exposure, • Excellent career progression opportunities, • Strong benefits package including bonus, healthcare and market-leading pension contribution For a confidential discussion or to apply, please contact Jackson Leonard today. Code: INDENM Please note as we receive a high level of applications we can only respond to applicants whose skills & qualifications are suitable for this position. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business. #J-18808-Ljbffr

The RoleJoining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at Harwell to support onshore mRNA vaccine production for respiratory diseases in the UK.This long term investment will create skilled jobs and strengthen collaboration with academic, NHS, and government partners. We welcome experts ready to help expand access to life saving vaccines.At Moderna's Harwell manufacturing facility, you will play a pivotal hands-on engineering role in introducing, commissioning, and optimising sophisticated automation systems supporting drug product packaging and drug substance manufacturing. You will help establish new automated labelling and secondary packaging capabilities while ensuring the reliability, compliance, and continuous improvement of existing Emerson DeltaV and Allen-Bradley/Rockwell PLC-based process control systems. Working independently as a technical specialist and collaborating across manufacturing, engineering, quality, validation, and digital teams, you will help translate advanced automation technology into safe, efficient, validated manufacturing operations, with opportunities to explore emerging digital and Generative AI-enabled solutions.Here’s What You’ll DoDrive packaging automation and manufacturing performance: Provide hands-on, day-to-day automation engineering support across drug product packaging and existing Drug Substance (DS) manufacturing operations. Troubleshoot and optimise PLCs, Emerson DeltaV distributed control systems, HMIs, instrumentation, industrial networks, machine controls, servo and motion systems, vision technologies, and equipment interfaces to maintain reliable manufacturing operations.Become a technical expert in automated packaging technologies: Support the introduction, operation, and continuous improvement of automated labelling and secondary packaging equipment, including labelers, cartoners, case packers, serialization and aggregation systems, vision inspection equipment, printers, scanners, conveyors, robotics, and material-handling systems. Develop a detailed understanding of equipment functionality, control architectures, and interfaces with wider manufacturing systems.Support packaging line configuration and operational readiness: Partner with manufacturing teams to manage equipment setup, format changes, line clearance, recipe management, and changeovers across different products and packaging configurations. Identify opportunities to simplify operations, reduce changeover times, and improve packaging-line consistency, flexibility, and throughput.Deliver automation projects from design through manufacturing start-up: Support new and modified automation systems throughout their complete engineering lifecycle, including design, Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), commissioning, qualification, validation, start-up, and handover to routine manufacturing. Contribute to new-equipment introduction, technology transfer, scale-up, and commercial manufacturing readiness.Strengthen process automation and control systems: Provide technical support for existing drug substance manufacturing automation, with particular emphasis on Emerson DeltaV and Allen-Bradley/Rockwell PLC-based systems. Diagnose complex control-system issues spanning instrumentation, electrical systems, industrial communications, automation logic, and mechanical equipment interfaces.Develop robust automation engineering documentation: Create, review, and maintain automation lifecycle documentation, including User Requirement Specification (URS) inputs, functional and design specifications, control strategies, configuration records, engineering drawings, risk assessments, Standard Operating Procedures (SOPs), troubleshooting guides, and engineering standards. Ensure documentation supports effective system operation, maintainability, and regulatory compliance.Collaborate with equipment manufacturers and system integrators: Work directly with Original Equipment Manufacturers (OEMs), automation suppliers, and system integrators to support equipment design, technical troubleshooting, upgrades, modifications, and performance improvements. Help ensure vendor-delivered solutions meet Moderna's operational, technical, safety, and quality expectations.Lead technical investigations and sustainable problem resolution: Independently investigate automation failures, recurring equipment downtime, quality events, and manufacturing process deviations. Apply structured root cause analysis to complex multidisciplinary problems, developing and implementing effective corrective and preventive actions (CAPAs) that address underlying causes and prevent recurrence.Use manufacturing data to improve equipment performance: Analyse equipment and process data to identify recurring failures, performance trends, and opportunities to improve equipment reliability, throughput, Overall Equipment Effectiveness (OEE), changeover performance, and operational robustness. Leverage manufacturing historians, MES, CMMS, and available analytics capabilities to support evidence-based engineering decisions.Maintain validated and compliant automation systems: Support GxP activities, including formal change controls, deviations, CAPAs, risk assessments, qualification, and validation. Partner closely with Quality and Validation to ensure packaging and process automation systems remain in a controlled and validated state throughout their operational lifecycle, with appropriate consideration of electronic records, data integrity, and computerized system requirements.Optimise equipment and systems integration: Troubleshoot interactions between packaging equipment, automation platforms, industrial networks, and plant-level digital systems. Contribute to robust communication and data exchange across operational technology (OT) and information technology (IT) environments, supporting equipment connectivity, serialization, and manufacturing-system integration.Drive reliability and lifecycle improvements: Contribute to equipment lifecycle management, preventive maintenance strategies, spare-parts planning, and technology obsolescence management. Apply reliability engineering principles to improve equipment availability, reduce unplanned downtime, and strengthen long-term manufacturing performance.Explore digital innovation and emerging technologies: Identify opportunities to leverage digital manufacturing tools, advanced analytics, and approved Generative AI-enabled solutions to support troubleshooting, technical knowledge management, engineering documentation, and equipment performance optimisation while maintaining appropriate GxP and data integrity controls.Collaborate across a multidisciplinary manufacturing environment: Work closely with Engineering, Manufacturing, Maintenance, Quality, Validation, Supply Chain, Automation, Digital, and external technical partners to deliver integrated packaging and process automation solutions that meet operational requirements, business objectives, and patient needs. Communicate complex technical findings clearly to manufacturing colleagues, technical stakeholders, leadership, and equipment vendors.Provide flexible manufacturing support: Take ownership of technical issues through resolution in a fast-paced manufacturing environment, balancing competing priorities and working independently. Provide occasional off-hours, weekend, and holiday support as manufacturing operations require.The key Moderna Mindsets you’ll need to succeed in the role:“We behave like owners. The solutions we’re building go beyond any job description.”"We digitize everywhere possible using the power of code to maximize our impact on patients.”Here’s What You’ll Need (Minimum Qualifications)Bachelor of Science degree in Mechanical Engineering, Electrical Engineering, Automation Engineering, Manufacturing Engineering, Packaging Engineering , or a related technical discipline.3+ years of automation engineering experience supporting manufacturing equipment, preferably within pharmaceutical, biotechnology, medical device, or another highly regulated industry.Demonstrated experience troubleshooting and supporting automated manufacturing or packaging equipment .Experience working within a GMP/GxP-regulated manufacturing environment .Ability to troubleshoot complex equipment problems involving multiple disciplines, including mechanical, electrical, controls, and automation systems.Experience supporting equipment changes through formal engineering and quality-system processes.Clear communication skills, with the ability to convey complex technical information in an understandable manner to manufacturing personnel, technical teams, leadership, vendors, and Quality stakeholders.Ability to work effectively in a fast-paced manufacturing environment and independently drive technical issues to resolution.Flexibility to occasionally provide off-hours, holiday, and weekend support as manufacturing needs require.Here’s What You’ll Bring to the Table (Preferred Qualifications)Strong knowledge of pharmaceutical drug product packaging operations and packaging-line equipment.Experience with packaging OEMs and technologies such as Marchesini, Optima, Syntegon/Bosch, Körber, Antares Vision, Cognex, Keyence, Zebra, Videojet, Domino, Rockwell Automation , or similar systems.Proficiency with Allen-Bradley/Rockwell PLCs, HMIs, servo systems, industrial networks, and machine controls .Experience with machine vision and automated inspection systems .Knowledge of serialization and aggregation requirements and associated Level 1–4 packaging architecture.Familiarity with 21 CFR Part 11, electronic records/electronic signatures, dataintegrity, and computerized system lifecycle principlesUnderstanding of packaging-related quality considerations such as label control, reconciliation, vision inspection, barcode grading, tamper evidence, container/closure integrity interfaces, and product traceability .Experience with Lean Manufacturing, Six Sigma, structured problem solving, FMEA, RCA, and reliability engineering methodologies .Experience using manufacturing data, historians, MES, CMMS, or analytics tools to improve equipment performance.Understanding of IT/OT networking and the ability to troubleshoot communication issues between equipment and plant systems.Knowledge of equipment lifecycle management, preventive maintenance, spare-parts strategies, and obsolescence management.Experience supporting new-equipment introduction, technology transfer, scale-up, and commercial manufacturing readiness.Ability to quickly learn new equipment, technologies, and manufacturing processes.A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative , consistent with the language in the existing role.As part of Moderna’s commitment to workplace safety, this role may require an enhanced pre-employment check.Our Working ModelAs we build our company, we have always believed that an in-person culture is critical to our success. This role is 100% onsite, reflecting the importance of being physically present to support the work, collaborate closely with colleagues, and contribute to our site-based operations.Working onsite enables real-time collaboration, strong team connections, direct mentorship, and the hands-on partnership needed to deliver our mission. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.Moderna is a smoke-free, alcohol-free, and drug-free work environment.Pay & BenefitsAt Moderna, we believe that when you feel your best, you can do your best work. That’s why our benefits and well-being resources are designed to support you—at work, at home, and everywhere in between.Competitive healthcare, plus voluntary benefit programs to support your unique needsA holistic approach to well-being with access to fitness, mindfulness, and mental health supportFamily building benefits, including fertility, adoption, and surrogacy supportGenerous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdownSavings and investments to help you plan for the futureLocation-specific perks and extrasThe benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.About ModernaSince our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!Moderna is committed to equal opportunity in employment and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.We’re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at .- #J-18808-Ljbffr

At the Ellison Institute of Technology (EIT), we're on a mission to translate scientific discovery into real world impact. We bring together visionary scientists, technologists, engineers, researchers, educators and innovators to tackle humanity's greatest challenges in four transformative areas: • Health, Medical Science & Generative Biology, • Food Security & Sustainable Agriculture, • Climate Change & Managing CO₂, • Artificial Intelligence & Robotics This is ambitious work - work that demands curiosity, courage, and a relentless drive to make a difference. At EIT, you'll join a community built on excellence, innovation, tenacity, trust, and collaboration, where bold ideas become real-world breakthroughs. Together, we push boundaries, embrace complexity, and create solutions to scale ideas from lab to society. Explore more at . Within this ecosystem, the Pathogen Mission exemplifies EIT's commitment to transformative science. It aims to revolutionise the diagnosis and treatment of infectious diseases by leveraging whole genome sequencing (WGS)-based metagenomic and pathogen-specific analytical tools. This remit includes the development of a decentralised, sample-to-answer sequencing diagnostic platform for infectious diseases, enabling rapid and accurate analysis of patient samples without prior assumptions. Supported by Oracle Inc.'s cloud-computing scale and security infrastructure, the Pathogen Mission is progressing towards certified diagnostic products for deployment in laboratories, hospitals, and public health organisations worldwide. We are seeking an experienced and innovative Senior Electronics R&D Engineer to develop advanced electronic interfaces, instrumentation, and measurement systems for next-generation nanopore sequencing technologies. This is a hands-on role within an ambitious early-stage development programme, taking technologies from proof of concept through to integrated, multi-channel sensing systems. Working closely with a Senior MEMS Development Engineer, you will design, build, and test experimental electronics, develop custom instrumentation, and optimise prototype devices through iterative development. Key areas of focus include precision analogue measurement, low-noise circuit design, multi-channel data acquisition, electronic control systems, and system integration. You will translate emerging concepts into working prototypes, identify technical limitations, and drive continuous improvement based on experimental data. The role also involves collaborating with external suppliers and technical partners, defining requirements, overseeing outsourced development, and evaluating resulting components and systems. As the programme grows, you will help establish the electrical engineering capabilities, testing infrastructure, and technical foundations needed to support a multidisciplinary development team. • Take technical ownership of the electrical engineering development of advanced electronic interfaces and measurement systems, from early concepts through to functional prototypes and integrated devices, • Design, build and commission custom electronic test equipment and experimental platforms to characterise electrical performance, reliability and repeatability, • Develop prototype electronic circuits and sensing architectures, including multi-channel analogue measurement systems, signal conditioning and data‑acquisition electronics, • Work closely with the Senior MEMS Development Engineer to co‑develop and evaluate prototype devices, using experimental findings to guide iterative improvements in device and instrumentation design, • Design and implement sensitive, low‑noise measurement systems capable of characterising electrical currents in the picoampere range, • Develop automated testing and data‑acquisition methods to assess electrical and sensing performance, including software for instrument control and data analysis, • Investigate electrical noise, leakage currents, signal integrity, parasitic effects and cross‑talk in multi‑channel sensing systems, • Develop and evaluate approaches to electrical grounding, shielding and electrostatic discharge (ESD) protection for sensitive electronic and electrochemical systems, • Collaborate with mechanical, MEMS and other engineering disciplines to develop experimental fixtures, prototype assemblies and integrated test platforms, • Design increasingly sophisticated electronic test platforms as the project progresses, supporting the transition from initial feasibility studies to integrated nanopore sensing systems, • Define technical requirements and specifications for external engineering suppliers, including the design and fabrication of custom electronics, components and specialist test equipment, • Coordinate technical activities with external suppliers and collaborators, reviewing designs, monitoring progress and evaluating deliverables against agreed performance requirements, • Plan and execute structured experiments, analyse performance data and translate findings into engineering requirements and design improvements, • Contribute to component selection, prototype fabrication, supplier engagement and assessments of manufacturability, scalability and cost, • Maintain clear technical documentation, design records and experimental results, contributing to intellectual property development and technical reviews while ensuring appropriate confidentiality, • Provide technical guidance and mentoring as the engineering team expands, helping establish robust engineering practices and development processes, • Degree in Electrical or Electronic Engineering, Physics or a related discipline, or equivalent relevant experience, • Significant experience in electronic engineering research and development, ideally involving novel instrumentation, sensor systems or precision measurement technologies, • Strong understanding of analogue and mixed‑signal electronics, including low‑noise circuit design, signal conditioning and measurement techniques, • Proven experience designing, building and debugging electronic hardware, including custom circuits, printed circuit boards and laboratory test systems, • Practical experience developing experimental instrumentation using laboratory equipment such as oscilloscopes, source‑measure units, precision current measurement systems and data‑acquisition hardware, • Experience developing or integrating electronic control, switching or multi‑channel measurement systems, • Ability to develop automated test methods, including scripting or programming for instrument control, data acquisition and analysis, • Experience planning and executing structured experimental programmes to characterise complex electronic systems and resolve technical challenges, • Strong understanding of electrical signal integrity, grounding, shielding and methods for minimising noise and interference, • Ability to work independently, establish technical direction and deliver working prototypes in an early‑stage R&D environment, • Experience collaborating with multidisciplinary teams and translating requirements between electronics, mechanical engineering and device fabrication, • Ability to develop clear technical specifications and work effectively with external engineering suppliers, development partners or specialist fabricators, • Experience with picoampere or similarly sensitive current measurements, including transimpedance amplifiers, leakage‑current management and low‑noise analogue front‑end design, • Knowledge of electrochemical sensing, biosensors, nanopore technologies or other low‑current sensor systems, • Experience with semiconductor devices, MEMS interfaces, microelectronic packaging or electronic sensor integration, • Familiarity with ASIC interfaces, FPGA‑based control, electronic multiplexing or multi‑channel sensor‑readout architectures, • Experience developing test equipment for evaluating the electrical performance and reliability of prototype devices, • Knowledge of ESD protection strategies for sensitive electronic devices or electrochemical sensors, • Experience with Python, LabVIEW or similar tools for automated test equipment, instrument control and data analysis, • Familiarity with precision PCB design techniques, guarding, shielding and control of parasitic capacitance, • Experience integrating prototype electronics with microfabricated devices, fluidic systems or other multidisciplinary hardware, • Experience working with external engineering companies or specialist suppliers to develop, fabricate and qualify custom components or instrumentation, • Understanding of design for manufacture, engineering reliability and transitioning prototype systems towards scalable production, • Hands‑on and inventive: Enjoys solving technical challenges through practical engineering, experimentation and rapid prototyping, • Comfortable with early‑stage R&D: Able to work effectively where solutions are not yet established and technical requirements evolve through experimentation, • Analytical and systematic: Uses sound engineering judgement and quantitative evidence to understand complex behaviour and guide design decisions, • Collaborative: Works closely with specialists in MEMS, mechanical engineering, chemistry and electronics, as well as external technical partners, to develop integrated solutions, • Independent and proactive: Can establish experimental capabilities, identify priorities and progress technical work with limited existing infrastructure, • Technically ambitious: Motivated by challenging engineering problems and developing technologies with the potential for substantial real‑world impact, • Clear communicator: Able to explain complex technical challenges, document findings and communicate requirements effectively with colleagues, suppliers and external collaborators, • Salary: Competitive + travel allowance + bonus, • Enhanced holiday pay, • Pension, • Life Assurance, • Income Protection, • Private Medical Insurance, • Hospital Cash Plan, • Therapy Services, • Perk Box, • Electric Car Scheme, • You must have the right to work permanently in the UK with a willingness to travel as necessary. In certain cases, we can consider sponsorship, and this will be assessed on a case‑by‑case basis, • You will live in, or within easy commuting distance of, Oxford (or be willing to relocate), • You must be eligible to work in the UK with occasional travel (1-3 trips per year) #J-18808-Ljbffr

At the Ellison Institute of Technology (EIT), we’re on a mission to translate scientific discovery into real world impact. We bring together visionaryscientists, technologists, engineers, researchers, educators and innovatorsto tackle humanity’s greatest challenges in four transformative areas: • Health, Medical Science & Generative Biology, • Food Security & Sustainable Agriculture, • Climate Change & Managing CO₂, • Artificial Intelligence & Robotics This is ambitious work - work that demands curiosity, courage, and a relentless drive to make a difference. At EIT, you’ll join a community built on excellence, innovation, tenacity, trust, and collaboration, where bold ideas become real-world breakthroughs. Together, we push boundaries, embrace complexity, and create solutions to scale ideas from lab to society. Explore more at . Welcome to the Pathogen Program Within this ecosystem, the Pathogen Mission exemplifies EIT’s commitment to transformative science. It aims to revolutionise the diagnosis and treatment of infectious diseases by leveraging whole genome sequencing (WGS)-based metagenomic and pathogen-specific analytical tools. This remit includes the development of a decentralised, sample-to-answer sequencing diagnostic platform for infectious diseases, enabling rapid and accurate analysis of patient samples without prior assumptions. Supported by Oracle Inc.’s cloud-computing scale and security infrastructure, the Pathogen Mission is progressing towards certified diagnostic products for deployment in laboratories, hospitals, and public health organisations worldwide. Your Role We are seeking an experienced and innovative Senior Electronics R&D Engineer to develop advanced electronic interfaces, instrumentation, and measurement systems for next-generation nanopore sequencing technologies. This is a hands-on role within an ambitious early-stage development programme, taking technologies from proof of concept through to integrated, multi-channel sensing systems. Working closely with a Senior MEMS Development Engineer, you will design, build, and test experimental electronics, develop custom instrumentation, and optimise prototype devices through iterative development. Key areas of focus include precision analogue measurement, low-noise circuit design, multi-channel data acquisition, electronic control systems, and system integration. You will translate emerging concepts into working prototypes, identify technical limitations, and drive continuous improvement based on experimental data. The role also involves collaborating with external suppliers and technical partners, defining requirements, overseeing outsourced development, and evaluating resulting components and systems. As the programme grows, you will help establish the electrical engineering capabilities, testing infrastructure, and technical foundations needed to support a multidisciplinary development team. Key Responsibilities • Take technical ownership of the electrical engineering development of advanced electronic interfaces and measurement systems, from early concepts through to functional prototypes and integrated devices., • Design, build and commission custom electronic test equipment and experimental platforms to characterise electrical performance, reliability and repeatability., • Develop prototype electronic circuits and sensing architectures, including multi-channel analogue measurement systems, signal conditioning and data-acquisition electronics., • Work closely with the Senior MEMS Development Engineer to co-develop and evaluate prototype devices, using experimental findings to guide iterative improvements in device and instrumentation design., • Design and implement sensitive, low-noise measurement systems capable of characterising electrical currents in the picoampere range., • Develop automated testing and data-acquisition methods to assess electrical and sensing performance, including software for instrument control and data analysis., • Investigate electrical noise, leakage currents, signal integrity, parasitic effects and cross-talk in multi-channel sensing systems., • Develop and evaluate approaches to electrical grounding, shielding and electrostatic discharge (ESD) protection for sensitive electronic and electrochemical systems., • Collaborate with mechanical, MEMS and other engineering disciplines to develop experimental fixtures, prototype assemblies and integrated test platforms., • Design increasingly sophisticated electronic test platforms as the project progresses, supporting the transition from initial feasibility studies to integrated nanopore sensing systems., • Define technical requirements and specifications for external engineering suppliers, including the design and fabrication of custom electronics, components and specialist test equipment., • Coordinate technical activities with external suppliers and collaborators, reviewing designs, monitoring progress and evaluating deliverables against agreed performance requirements., • Plan and execute structured experiments, analyse performance data and translate findings into engineering requirements and design improvements., • Contribute to component selection, prototype fabrication, supplier engagement and assessments of manufacturability, scalability and cost., • Maintain clear technical documentation, design records and experimental results, contributing to intellectual property development and technical reviews while ensuring appropriate confidentiality., • Provide technical guidance and mentoring as the engineering team expands, helping establish robust engineering practices and development processes. Knowledge, Skills and Experience We welcome applicants from industry, applied research and academia who can demonstrate strong technical expertise and practical engineering capability. • Degree in Electrical or Electronic Engineering, Physics or a related discipline, or equivalent relevant experience., • Significant experience in electronic engineering research and development, ideally involving novel instrumentation, sensor systems or precision measurement technologies., • Strong understanding of analogue and mixed-signal electronics, including low-noise circuit design, signal conditioning and measurement techniques., • Proven experience designing, building and debugging electronic hardware, including custom circuits, printed circuit boards and laboratory test systems., • Practical experience developing experimental instrumentation using laboratory equipment such as oscilloscopes, source-measure units, precision current measurement systems and data-acquisition hardware., • Experience developing or integrating electronic control, switching or multi-channel measurement systems., • Ability to develop automated test methods, including scripting or programming for instrument control, data acquisition and analysis., • Experience planning and executing structured experimental programmes to characterise complex electronic systems and resolve technical challenges., • Strong understanding of electrical signal integrity, grounding, shielding and methods for minimising noise and interference., • Ability to work independently, establish technical direction and deliver working prototypes in an early-stage R&D environment., • Experience collaborating with multidisciplinary teams and translating requirements between electronics, mechanical engineering and device fabrication., • Ability to develop clear technical specifications and work effectively with external engineering suppliers, development partners or specialist fabricators. Desirable Knowledge, Skills and Experience • Experience with picoampere or similarly sensitive current measurements, including transimpedance amplifiers, leakage-current management and low-noise analogue front-end design., • Knowledge of electrochemical sensing, biosensors, nanopore technologies or other low-current sensor systems., • Experience with semiconductor devices, MEMS interfaces, microelectronic packaging or electronic sensor integration., • Familiarity with ASIC interfaces, FPGA-based control, electronic multiplexing or multi-channel sensor-readout architectures., • Experience developing test equipment for evaluating the electrical performance and reliability of prototype devices., • Knowledge of ESD protection strategies for sensitive electronic devices or electrochemical sensors., • Experience with Python, LabVIEW or similar tools for automated test equipment, instrument control and data analysis., • Familiarity with precision PCB design techniques, guarding, shielding and control of parasitic capacitance., • Experience integrating prototype electronics with microfabricated devices, fluidic systems or other multidisciplinary hardware., • Experience working with external engineering companies or specialist suppliers to develop, fabricate and qualify custom components or instrumentation., • Understanding of design for manufacture, engineering reliability and transitioning prototype systems towards scalable production. Key Attributes • Hands-on and inventive: Enjoys solving technical challenges through practical engineering, experimentation and rapid prototyping., • Comfortable with early-stage R&D: Able to work effectively where solutions are not yet established and technical requirements evolve through experimentation., • Analytical and systematic: Uses sound engineering judgement and quantitative evidence to understand complex behaviour and guide design decisions., • Collaborative: Works closely with specialists in MEMS, mechanical engineering, chemistry and electronics, as well as external technical partners, to develop integrated solutions., • Independent and proactive: Can establish experimental capabilities, identify priorities and progress technical work with limited existing infrastructure., • Technically ambitious: Motivated by challenging engineering problems and developing technologies with the potential for substantial real-world impact., • Clear communicator: Able to explain complex technical challenges, document findings and communicate requirements effectively with colleagues, suppliers and external collaborators. Our Benefits: • Salary: Competitive + travel allowance + bonus, • Enhanced holiday pay, • Pension, • Life Assurance, • Income Protection, • Private Medical Insurance, • Hospital Cash Plan, • Therapy Services, • Perk Box, • Electric Car Scheme Working Together – What It Involves: • You must have the right to work permanently in the UK with a willingness to travel as necessary. In certain cases, we can consider sponsorship, and this will be assessed on a case-by-case basis., • You will live in, or within easy commuting distance of, Oxford (or be willing to relocate)., • You must be eligible to work in the UK with occasional travel (1-3 trips per year). #J-18808-Ljbffr

IonQ, Inc . [NYSE: IONQ] is the world's leading quantum platform and merchant supplier - delivering integrated quantum solutions across computing, networking, sensing, and security. IonQ's newest generation of quantum computers, the IonQ Tempo, is the latest in a line of cutting-edge systems that have been helping customers and partners including Amazon Web Services, and AstraZeneca achieve 20x performance results and accelerate innovation in drug discovery, materials science, financial modeling, logistics, cybersecurity, and defense. In 2025, the company achieved 99.99% two-qubit gate fidelity, setting a world record in quantum computing performance . Headquartered in College Park, Maryland, IonQ has operations in California, Colorado, Massachusetts, Tennessee, Washington, Italy, South Korea, Sweden, Switzerland, Canada, and the United Kingdom. Our quantum computing services are available through all major cloud providers, while we also meet the needs of networking and sensing customers across land, sea, air, and space. IonQ is making quantum platforms more accessible and impactful than ever before. Oxford, England, UK Hybrid We are looking for a Senior Silicon Validation Engineer to join our Cryo-CMOS IC team at IonQ Oxford. You will lead the validation and characterisation of analogue and mixed-signal ASICs for our trapped-ion quantum processors, from test planning and platform development through first-silicon bring-up, debug and system integration. This is a hands-on technical role. You will shape our validation architecture, build reusable hardware and software, and provide the evidence needed to make confident silicon acceptance decisions. The work includes room-temperature silicon validation and silicon characterisation at cryogenic temperatures (around 4 kelvin), on packaged parts, chip-on-board assemblies and bare die on a cryogenic probe station. You will own validation delivery across chip and system interfaces, working closely with analogue and digital design, verification, modelling, firmware and systems engineers. You will turn requirements into measurable tests, prepare platforms before silicon arrives and resolve failures across the chip, board and software. As a Senior engineer, you will set technical standards, guide other engineers and improve coverage, repeatability and test efficiency across successive ASIC generations. Key responsibilities include: • Own the silicon validation strategy, plans, acceptance criteria and readiness reviews, with traceability from block and system requirements to tests, results and unresolved risks., • Present the silicon acceptance report to the Cryo-CMOS IC Lead and programme stakeholders., • Lead first-silicon bring-up and characterisation of sample-and-hold and switch arrays, DACs, ADCs, references, amplifiers, switches, regulators, clocking and device-level test structures, across supply, temperature, operating modes and device variation, with sound calibration and measurement uncertainty., • Develop validation boards, fixtures and reusable Python automation, instrument drivers and regression suites, addressing signal integrity, grounding, power integrity and measurement access, with version-controlled tests and reproducible data analysis., • Plan and lead cryogenic measurements with specialist colleagues, including bare-die probing and the cold signal chain, and drive failures to root cause, separating silicon defects from board, firmware and test artefacts and correlating results with simulations, device models and foundry or partner data., • Influence testability before tape-out, coordinate validation with external design partners, the foundry and other IonQ sites., • Lead technical reviews, mentor engineers and document methods to improve throughput, data quality and reuse. You will bring substantial experience in analogue or mixed-signal silicon validation and characterisation, with ownership of multiple silicon bring-up programmes. A degree in electrical or electronic engineering, or equivalent practical experience, is expected. You should combine hands-on laboratory skills with sound judgement on test coverage, measurement confidence and programme risk. You'd be a great fit with: • Strong electronics fundamentals and experience validating precision signal chains, data converters or power-management circuits, including their digital control interfaces., • Practical expertise with oscilloscopes, precision sources and meters, signal generators, spectrum and logic analysers; confidence designing reliable low-noise, low-leakage measurements., • Strong Python programming for instrument control, automated testing and statistical analysis; disciplined use of Git or equivalent version control and maintainable test software., • Experience designing and debugging test PCBs, reviewing layouts and working with interfaces such as SPI, I2C, JTAG and custom shift-register chains, alongside embedded firmware or FPGA-based platforms., • A record of resolving complex chip, board and software interactions through structured experiments and collaboration., • Experience leading technical projects, mentoring engineers and communicating evidence, uncertainty and decisions in clear written reports. Useful additional experience includes cryogenic or other extreme-temperature testing; wafer or bare-die probing; early-stage IP or test-chip evaluation; FPGA development and C/C++; circuit simulation; and production test correlation. Prior quantum computing is welcome but not required. • Be part of a team that's shaping the future of quantum. We offer more than just a role, you'll join a world class community of scientists, engineers and innovators working to unlock the full potential of quantum computing., • We offer a range of benefits, including opportunities to further your career alongside industry leaders, a competitive salary with IonQ stock options, an annual performance bonus, generous annual leave, flexible hybrid working, private medical and dental insurance for you and your family, and much more., • Join us and be part of the future of quantum computing., • Compensation will vary based on individual factors such as education, qualifications, and experience of the final candidate(s), specific office location, and calibration against relevant market data and internal team equity. Posted base salary figures are subject to change as new market data becomes available. Our benefits include comprehensive medical, dental, and vision plans, matching 401(k), unlimited PTO and paid holidays, parental/adoption leave, legal insurance, and a home technology stipend. Details of participation in these benefit plans will be provided when a candidate receives an offer of employment., • At IonQ, we believe in fair treatment, access, opportunity, and advancement for all while striving to identify and eliminate barriers. We empower employees to thrive by fostering a culture of autonomy, productivity, and respect. We are dedicated to creating an environment where individuals can feel welcomed, respected, supported, and valued. We're proud to be an equal opportunity employer and welcome applicants from all backgrounds. We are committed to equity and justice. We welcome different voices and viewpoints and do not discriminate on the basis of race, religion, ancestry, physical and/or mental disability, medical condition, genetic information, marital status, sex, gender, gender identity, gender expression, transgender status, age, sexual orientation, military or veteran status, or any other basis protected by law. We are proud to be an Equal Employment Opportunity employer. The position you are applying for will require access to technology that is subject to U.S. export control and government contract restrictions. Employment with IonQ is contingent on either verifying "U.S. Person" (e.g., U.S. citizen, U.S. national, U.S. permanent resident, or lawfully admitted into the U.S. as a refugee or granted asylum) status for export controls and government contracts work, obtaining any necessary license, and/or confirming the availability of a license exception under U.S. export controls. Please note that in the absence of confirming you are a U.S. Person for export control and government contracts work purposes, IonQ may choose not to apply for a license or decline to use a license exception (if available) for you to access export-controlled technology that may require authorization, and similarly, you may not qualify for government contracts work that requires U.S. Persons, and IonQ may decline to proceed with your application on those bases alone. Accordingly, we will have some additional questions regarding your immigration status that will be used for export control and compliance purposes, and the answers will be reviewed by compliance personnel to ensure compliance with federal law. Due to applicable export control laws and regulations, candidates must be a U.S. citizen or national, U.S. permanent resident (i.e., current Green Card holder), or lawfully admitted into the U.S. as a refugee or granted asylum. Accordingly, we will have some additional questions regarding your immigration status that will be used for export control and compliance purposes, and the answers will be reviewed by compliance personnel to ensure compliance with federal law. #J-18808-Ljbffr

OrganOx is an innovative, fast-paced, global medical device company with a mission to save lives by making every donated organ count. We are a commercial stage organ technology company, spun out of the University of Oxford in 2008, committed to improving transplantation outcomes throughout the world. The company's first product, the OrganOx metra normothermic machine perfusion (NMP) system for liver transplantation, has been used to support more than 5,000 liver transplant operations globally. Position Summary The Systems Test Architect provides technical and strategic leadership on design, development and test. Driving a culture of innovation, technical excellence and delivery responsibility; enabling efficient development of cutting-edge Class 3 Medical Devices in an ISO 13485, 21 CFR PART 820 and MDR quality management system environment. This is an onsite position based in Oxford with flexibility. Major Responsibilities • Author and maintain the System Test strategy and roadmap of developments, • Conducting the analysis, trending and insight generation of insights to identify risks and capitalize on opportunities, • Lead activities for high level system design, through all stages of technical development and across the business structure in with company goals and technology strategies, • Ensuring test design and testability input to enable DfT and DfR of System, Mechanical, Electronic, Software and Digital Health designs., • Researching technologies and making informed recommendations for their introduction based on best practice and project/company goals, • Comprehensive system test of designs in the product and project portfolio to ensure criteria are met across a range of attributes including function, performance, safety, interface and reliability, • Collaborate with and advise key stakeholders to gather and understand needs and technical specifications, working closely to ensure alignment., • Supporting, coaching and mentoring engineers across the business in the development of their Knowledge, Skills and Abilities, • System Test Engineering SOP & WI that enable Design Verification and Validation. Including Plans, Sample Sizing, Methods, Protocols, training, execution, analysis and reporting, • Selection recommendations, development and qualification of tools and systems, • Integrating relevant DHF content and technical activities for products across the project portfolio to achieve efficient, compliant delivery., • Contributing to performance metrics and their review, identifying improvement opportunities and implementing development plans, • Collaborate with colleagues, teams throughout the business and external resources to ensure adherence to architectural guidelines, best practice and timely execution., • Supporting engineers with completion of the relevant records for test activities in the DHF, DMR and DHR; facilitating the regulatory submission process and ensuring the capability for future development and maintenance of designs., • Adhere to the letter and spirit of OrganOx's Code of Conduct and all other company policies Requirements Skills & Experience • Extensive experience in developing test strategies, infrastructure, and tool qualifications, • Hands-on experience working with external test houses to ensure compliance with IEC 60601 standards, • Strong understanding of sample size development and statistical justification, • Experience with audits and regulatory submissions, including preparation and presentations to regulatory bodies, • Experience with software driven mechatronic devices, precision control and hydraulics., • Experience with Class 2 or 3 medical devices and familiarity with the unique challenges in this field are desirable, • Advanced knowledge of medical device testing tools and technologies (desirable), • Exceptional communication and leadership skills with a collaborative mindset, • Demonstrable knowledge of the regulatory environment, including FDA, IEC 60601, ISO 13485, ISO 62366 and other relevant standards Qualifications • Bachelor's or Master's degree in Engineering, Biomedical Sciences, or a related field, • A well established and proven track record in systems testing within the medical device industry, preferably with Class 3 devices Benefits At OrganOx, we value innovation, evidence, integrity, teamwork, respect, and passion. We offer competitive compensation and comprehensive benefits, including healthcare and retirement plans. We support work-life balance and provide opportunities for ongoing professional development. We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to age, disability, gender reassignment, marriage and civil partnership, pregnancy and maternity, race, religion or belief, sex, sexual orientation race, or any other characteristics protected by law. #J-18808-Ljbffr

At the Ellison Institute of Technology (EIT), we’re on a mission to translate scientific discovery into real world impact. We bring together visionaryscientists, technologists, engineers, researchers, educators and innovatorsto tackle humanity’s greatest challenges in four transformative areas: • Health, Medical Science & Generative Biology, • Food Security & Sustainable Agriculture, • Climate Change & Managing CO₂, • Artificial Intelligence & Robotics This is ambitious work - work that demands curiosity, courage, and a relentless drive to make a difference. At EIT, you’ll join a community built on excellence, innovation, tenacity, trust, and collaboration, where bold ideas become real-world breakthroughs. Together, we push boundaries, embrace complexity, and create solutions to scale ideas from lab to society. Explore more at www.eit.org. Welcome to the Pathogen Project: Within this ecosystem, the Pathogen Mission exemplifies EIT’s commitment to transformative science. It aims to revolutionise the diagnosis and treatment of infectious diseases by leveraging whole genome sequencing (WGS)-based metagenomic and pathogen-specific analytical tools. This remit includes the development of a decentralised, sample-to-answer sequencing diagnostic platform for infectious diseases, enabling rapid and accurate analysis of patient samples without prior assumptions. Supported by Oracle Inc.’s cloud-computing scale and security infrastructure, the Pathogen Mission is progressing towards certified diagnostic products for deployment in laboratories, hospitals, and public health organisations worldwide. Your Role: At EIT we are seeking an experienced and detail orientated Microfluidics Engineer / Scientist to help develop next-generation diagnostic technology. In this role, you’ll work alongside experts in microfluidics, microbiology, electronics and firmware to design, build and iterate prototype instrumentation for a point-of-care device capable of metagenomic sequencing through a microfluidic cartridge interface. You will take a hands-on role in translating microfluidic workflows into robust, system-ready implementations, working at the interface between cartridge design and automated instrumentation. This will involve designing and running experiments, supporting integration of microfluidic systems with actuation and control hardware, and resolving real-world challenges related to fluid behavior, timing, sealing and system interaction. You will contribute directly to the development of decentralised diagnostic systems aimed at improving infectious disease detection in hospitals and public health settings worldwide. Key Responsibilities: • Design, develop and improve microfluidic systems and cartridge architectures for use within automated instrumentation., • Translate biological assay requirements into practical microfluidic designs suitable for automation., • Define and refine interfaces between cartridge and instrument, including fluidic, mechanical and thermal interactions., • Ensure cartridge designs remain compatible with automation, sensing and actuation strategies throughout development and system integration., • Collaborate with instrumentation, electronics and firmware engineers to ensure cartridge designs work effectively with automated actuation and control systems., • Support integration of microfluidic cartridges into prototype systems, including hands-on testing, troubleshooting and system-level validation., • Prototype and test microfluidic designs using appropriate fabrication techniques, such as soft lithography, machining and rapid prototyping., • Design and execute experiments to evaluate cartridge performance, including yield, efficiency and repeatability., • Identify and help resolve fluidic, mechanical and assay-related failure modes., • Contribute to improving robustness, manufacturability and ease of use of cartridge designs., • Document designs, test results and iteration outcomes clearly and systematically., • Contribute to design reviews and technical decision-making within the microfluidics domain. Knowledge, Skills and Experience: We welcome applicants with a range of experiences and career paths. You may have gained relevant expertise in industry, applied research or academia. • BSc or BEng (or equivalent) in Engineering, Physics, Bioengineering, or related field with specialisation in microfluidics, MEMS, or lab-on-a-chip systems, • 4+ years’ experience in microfluidics, lab-on-chip systems, or related areas (industry or applied research)., • Experience designing and developing microfluidic systems, devices or closely related technologies., • Understanding of fluid behaviour at small scales, including areas such as mixing, flow control or multiphase systems., • Experience working with biological or chemical assays, ideally within microfluidic or closely related systems., • Practical experience in prototyping and testing devices or experimental systems., • Experience designing for integration with external systems, such as actuators, pumps or thermal systems., • Ability to design and run structured experiments to evaluate system performance., • Experience troubleshooting and improving performance in complex systems., • Familiarity with CAD or similar design tools., • Strong problem-solving skills and a practical approach to experimental work., • Ability to work effectively within multidisciplinary teams spanning engineering, biology and software. We recognise that candidates may not meet every listed criterion. If your experience aligns with most of the requirements and you are motivated by the mission, we encourage you to apply. Desirable Knowledge, Skills and Experience: • Experience designing microfluidic systems for automated or semi-automated platforms., • Knowledge of sample preparation workflows, such as nucleic acid extraction, host depletion or amplification., • Familiarity with bead-based workflows, particle separation or cell lysis techniques., • Experience working with complex biological samples, such as blood, sputum or environmental samples., • Understanding of contamination control and sample handling in diagnostic systems., • Experience considering manufacturability and scale-up of microfluidic designs., • Familiarity with cartridge-based or disposable device design., • Exposure to integration of microfluidics with sensors or detection systems., • Experience working in research and development or product development environments. Key Attributes: • Enjoys hands-on experimental and engineering work, including building, testing and iterating real systems., • Comfortable working in an R&D environment where priorities can evolve., • Approaches technical challenges thoughtfully and systematically., • Collaborative and team-oriented, working effectively with engineers, scientists and software developers., • Able to translate scientific concepts into robust engineering solutions., • Detail-oriented and methodical in experimental design, testing and documentation., • Able to work independently within their area of expertise while contributing to wider team goals., • Communicates technical challenges and solutions clearly across disciplines. Our Benefits: • Salary: Competitive + travel allowance + bonus, • Enhanced holiday pay, • Pension, • Life Assurance, • Income Protection, • Private Medical Insurance, • Hospital Cash Plan, • Therapy Services, • Perk Box, • Electric Car Scheme Working Together – What It Involves: • You must have the right to work permanently in the UK with a willingness to travel as necessary. In certain cases, we can consider sponsorship, and this will be assessed on a case-by-case basis., • You will live in, or within easy commuting distance of, Oxford (or be willing to relocate)., • You must be eligible to work in the UK with occasional travel (1-3 trips per year). #J-18808-Ljbffr

At the Ellison Institute of Technology (EIT), we’re on a mission to translate scientific discovery into real world impact. We bring together visionary scientists, technologists, engineers, researchers, educators and innovators to tackle humanity’s greatest challenges in four transformative areas: • Health, Medical Science & Generative Biology, • Food Security & Sustainable Agriculture, • Climate Change & Managing CO₂, • Artificial Intelligence & Robotics This is ambitious work - work that demands curiosity, courage, and a relentless drive to make a difference. At EIT, you’ll join a community built on excellence, innovation, tenacity, trust, and collaboration, where bold ideas become real-world breakthroughs. Together, we push boundaries, embrace complexity, and create solutions to scale ideas from lab to society. Explore more at . Within this ecosystem, the Pathogen Mission exemplifies EIT’s commitment to transformative science. It aims to revolutionise the diagnosis and treatment of infectious diseases by leveraging whole genome sequencing (WGS)-based metagenomic and pathogen-specific analytical tools. This remit includes the development of a decentralised, sample-to-answer sequencing diagnostic platform for infectious diseases, enabling rapid and accurate analysis of patient samples without prior assumptions. Supported by Oracle Inc.’s cloud-computing scale and security infrastructure, the Pathogen Mission is progressing towards certified diagnostic products for deployment in laboratories, hospitals, and public health organisations worldwide. We're seeking an experienced and innovative Senior MEMS Development Engineer/Scientist to develop novel microfabricated devices and sensor interfaces for next-generation nanopore sequencing technologies. This hands-on role will focus on designing, prototyping, and characterising MEMS devices, taking concepts from proof-of-concept through to integrated multi-channel sensing systems. Working closely with a Senior Electronics R&D Engineer, you'll drive device development through iterative design, testing, and optimisation. You’ll tackle challenges spanning microfabrication, materials, device architecture, and MEMS-electronics integration while collaborating with external fabrication partners and technical suppliers. As the programme grows, you’ll help establish the MEMS engineering capabilities, processes, and technical foundations needed to support a wider multidisciplinary team. • Take technical ownership of the MEMS engineering development of novel microfabricated sensing structures and device interfaces, from early concepts through to functional prototypes and integrated systems., • Design and develop microfabricated devices and test structures, including the selection of materials, fabrication processes and device geometries., • Develop and evaluate fabrication approaches using established semiconductor and MEMS manufacturing techniques, adapting processes to meet the requirements of novel sensing devices., • Work closely with the Senior Electrical R&D Engineer to co-develop and evaluate prototype devices, using experimental findings to guide iterative improvements in MEMS design and electronic integration., • Design and characterise mechanical, electrical and material interfaces, investigating their influence on device performance, reliability and repeatability., • Develop experimental methods and test structures to assess fabrication quality, dimensional accuracy, device performance and reliability., • Investigate the effects of materials, surface properties, fabrication tolerances and assembly processes on device behaviour and performance., • Collaborate with electrical and mechanical engineers to develop prototype assemblies, alignment methods and experimental test platforms., • Identify and resolve fabrication challenges through design iteration, experimental characterisation and failure analysis., • Develop increasingly sophisticated prototype devices as the project progresses, supporting the transition from initial feasibility studies to integrated nanopore sensing systems., • Identify and engage specialist external fabrication facilities, engineering suppliers and technical collaborators to support the development and manufacture of prototype components and devices., • Define technical specifications and fabrication requirements for external suppliers, including design documentation, material requirements, dimensional tolerances and performance criteria., • Coordinate technical activities with external suppliers and collaborators, reviewing fabrication approaches, monitoring progress and evaluating deliverables against agreed requirements., • Plan and execute structured experiments, analyse performance data and translate findings into engineering requirements and design improvements., • Contribute to the selection and development of fabrication methods, considering manufacturability, scalability, cost and process reliability., • Maintain clear technical documentation, design records and experimental results, contributing to intellectual property development and technical reviews while ensuring appropriate confidentiality., • Provide technical guidance and mentoring as the engineering team expands, helping establish robust engineering practices and development processes. We welcome applicants from industry, applied research and academia who can demonstrate strong technical expertise and practical engineering capability. • Degree in Electrical Engineering, Mechanical Engineering, Materials Science, Physics or a related discipline, or equivalent relevant experience., • Significant experience in MEMS engineering, semiconductor microfabrication or microdevice development, ideally involving novel sensors, electronic interfaces or precision microfabricated systems., • Strong understanding of MEMS design principles, materials selection and microfabrication techniques., • Experience designing microfabricated devices using CAD tools, including the preparation of layouts, fabrication drawings or photolithography mask designs., • Practical knowledge of semiconductor and MEMS manufacturing processes, such as photolithography, thin-film deposition, etching, surface treatment and metallisation., • Experience developing and characterising prototype devices, including dimensional, mechanical and electrical evaluation., • Ability to understand and resolve fabrication challenges through experimental investigation, design modification and process optimisation., • Knowledge of material properties, fabrication tolerances and their influence on device functionality and reliability., • Experience planning and executing structured experimental programmes to characterise complex devices and resolve technical challenges., • Ability to work independently, establish technical approaches and deliver functional prototypes in an early-stage R&D environment., • Experience collaborating with multidisciplinary teams and translating requirements between MEMS, electronics, mechanical engineering and device fabrication., • Ability to develop clear technical specifications and work effectively with external fabrication facilities, engineering suppliers or development partners., • Experience developing MEMS or microfabricated devices for biosensing, electrochemical sensing, nanopore technologies or other sensor applications., • Knowledge of silicon micromachining, wafer processing and microelectronic device fabrication., • Experience with microfabricated electrodes, conductive thin films, dielectric materials or electronic sensor interfaces., • Familiarity with microelectronic packaging, device assembly, bonding and integration of MEMS with electronic systems., • Experience with polymeric materials, elastomeric components or other compliant materials used in microsystems., • Knowledge of mechanical contact behaviour, surface interactions, material deformation and reliability testing at small length scales., • Experience with optical microscopy, electron microscopy, profilometry, surface analysis or other microdevice characterisation techniques., • Experience designing devices that incorporate fluidic, electrochemical or biological components., • Familiarity with finite element analysis or other simulation methods for mechanical, thermal or material behaviour., • Experience working with external MEMS foundries, academic cleanroom facilities or specialist microfabrication suppliers., • Knowledge of fabrication process development, process yield improvement and quality control., • Understanding of design for manufacture, engineering reliability and transitioning prototype devices towards scalable production., • Hands-on and inventive: Enjoys solving technical challenges through practical engineering, experimentation and rapid prototyping., • Comfortable with early-stage R&D: Able to work effectively where solutions are not yet established and technical requirements evolve through experimentation., • Analytical and systematic: Uses sound engineering judgement and quantitative evidence to understand complex behaviour and guide design decisions., • Collaborative: Works closely with specialists in electronics, mechanical engineering, chemistry and MEMS fabrication, as well as external technical partners, to develop integrated solutions., • Independent and proactive: Can establish experimental capabilities, identify priorities and progress technical work with limited existing infrastructure., • Technically ambitious: Motivated by challenging engineering problems and developing technologies with the potential for substantial real-world impact., • Clear communicator: Able to explain complex technical challenges, document findings and communicate requirements effectively with colleagues, suppliers and external collaborators., • Salary: Competitive + travel allowance + bonus, • Enhanced holiday pay, • Pension, • Life Assurance, • Income Protection, • Private Medical Insurance, • Hospital Cash Plan, • Therapy Services, • Perk Box, • Electric Car Scheme, • You must have the right to work permanently in the UK with a willingness to travel as necessary. In certain cases, we can consider sponsorship, and this will be assessed on a case-by-case basis., • You will live in, or within easy commuting distance of, Oxford (or be willing to relocate)., • You must be eligible to work in the UK with occasional travel (1-3 trips per year). #J-18808-Ljbffr

Location: Oxfordshire Type: Full-time, Permanent - Fully on site We are looking for a hands-on Production Engineer to assist with the scale-up, industrialisation, and day-to-day manufacturing support of our next-generation fluidic products. Working alongside senior engineers, you will bridge the gap between R&D and production by building, wiring, and commissioning assembly fixtures, automated test equipment, and robotic cells. • Process Scale-Up: Support the transfer of new products into production, tuning processes like precision dispensing, laser welding, and leak testing., • Workshop & Hardware: Build, wire, debug, and maintain mechanical fixtures, electrical enclosures, sensors, and basic PLC/HMI controls., • Validation & Quality: Assist with equipment validation (FAT/SAT, IQ/OQ/PQ) and continuous improvement using root-cause analysis and SPC tools., • Background: Degree or apprenticeship in Mechanical, Electrical, Automation, or Mechatronics Engineering., • Practical Skills: Hands-on workshop experience wiring, building, and troubleshooting electromechanical machinery., • Technical Basics: Familiarity with 3D CAD, electrical schematics, and industrial sensors/actuators., • Bonus Points: Exposure to medical device/biotech standards (ISO 13485), basic robotics, or precision fluid handling #J-18808-Ljbffr

This is an exciting time to join an established and internationally respected medical device company with a long history of developing and producing highly regarded medical equipment. Now part of a larger international medical technology group, the business is entering an important period of investment, new product introduction and production development. Alongside the continued production and evolution of the products for which the company is renowned, the business is preparing for the introduction of next‑generation and entirely new products, creating significant opportunities to develop the production operation in Abingdon. As Production Engineering Team Lead, you will be at the centre of this change. This is not simply a role focused on maintaining today's production environment. We are looking for someone who can help define how tomorrow's products will be produced - developing existing production processes, introducing new methods and technologies, establishing and improving production lines, and ensuring that new products move successfully from development into efficient, repeatable and high‑quality production. The successful individual will inherit an experienced Production Engineering team and an established production environment. The challenge will be to preserve what works well while identifying where things can be done differently and better. We are therefore looking for a creatively minded and practically orientated engineering leader: someone who is comfortable challenging existing methods, evaluating new tools and technologies, and turning ideas into sustainable improvements in quality, productivity, cost, capacity and production performance. To lead and develop the Production Engineering team, managing its workload, priorities and technical resources while providing effective engineering support across the wider production operation. The Production Engineering Team Lead will work closely with Production, NPD, Quality & Regulatory, Purchasing/Sourcing and other functions to support existing products while playing a key role in the industrialisation and introduction of new products into the Abingdon production facility. The position will combine hands‑on engineering leadership with longer‑term responsibility for improving production capability, processes and methods. A central objective will be to ensure that Production Engineering is not simply responding to today's production problems, but is actively preparing the business for future products, increased production requirements and continued growth. • Lead the day‑to‑day activities of the Production Engineering department and directly manage a team of five Production Engineers., • Establish clear priorities, objectives and workloads for the team, balancing immediate production requirements with longer‑term engineering and improvement projects., • Work closely with the Production department to resolve day‑to‑day issues and minimise disruption to output., • Provide engineering leadership for the introduction of new products into production, working closely with NPD from the development stage through industrialisation, validation, production launch and subsequent volume production., • Support the creation, modification and optimisation of production lines for both new and existing products, considering quality, ergonomics, workflow, capacity, efficiency, cost and scalability., • Review existing production methods and identify opportunities to introduce new processes, tooling, equipment, automation and production technologies where these can improve quality, productivity or cost., • Champion a culture of continuous improvement, using appropriate Lean Manufacturing, problem‑solving and process‑improvement techniques to identify and eliminate waste and improve production performance., • Review and investigate rejected parts, assemblies and production failures, establishing root causes and implementing robust corrective actions., • Support production change control and associated software/system testing., • Develop and support cost‑down and value‑improvement initiatives across existing products and production processes without compromising product quality or regulatory compliance., • Develop and support test protocols and the validation of new or modified parts, assemblies, production equipment and processes., • Work closely with Purchasing and Sourcing on the evaluation and approval of new and revised components and samples., • Support the qualification and validation of new suppliers, processes and products, including visits to supplier facilities where appropriate., • Provide engineering support throughout the lifecycle of established products, including component obsolescence, supplier changes, quality variation, test issues and opportunities for functional or production improvement., • Work collaboratively with Quality & Regulatory on complaint investigations, root‑cause analysis, CAPA activity and the implementation of sustainable corrective and preventative actions., • Develop appropriate production strategies for new product introductions, considering tooling, fixtures, test equipment, process capability, production layout, documentation, training and capacity requirements., • Identify opportunities to improve the use of production data, systems and engineering tools to support better decision‑making and performance., • Ensure that production processes are robust, repeatable and capable of delivering the required standards of product quality and output., • Develop effective relationships across Engineering, NPD, Production, Quality, Regulatory, Supply Chain and Purchasing, ensuring Production Engineering is involved early enough to influence product and process decisions. A key part of the position is the leadership and development of the Production Engineering team. • Coach, mentor and develop the five Production Engineers, identifying individual development needs and opportunities to broaden technical capability., • Create an environment in which engineers are encouraged to question existing processes, propose improvements and take ownership of engineering problems., • Develop the capability of the department so that it can successfully support both the established product portfolio and the next generation of products entering production., • Establish clear priorities and accountability while encouraging collaboration and knowledge sharing., • Build strong relationships with the wider production workforce, including assembly, calibration, test and quality personnel. We are interested in an engineer who combines strong production engineering knowledge with leadership ability and an improvement mindset. You are likely to have: • A Degree, HNC or equivalent qualification in Mechanical, Production, Manufacturing, Electronics or another relevant engineering discipline., • At least five years' experience within a design, production or engineering environment., • Experience of leading, supervising or developing engineers within a production environment., • Strong practical understanding of production processes, Production Engineering and the introduction or improvement of production equipment, tooling and processes., • Experience of New Product Introduction (NPI/NPD) and industrialisation, ideally taking products from engineering development through validation and into production., • Demonstrable experience of continuous improvement, Lean Manufacturing, root‑cause analysis and structured problem solving., • An ability to examine an established production process objectively - recognising what should be retained while identifying where technology, process or working practices could be improved., • Strong analytical and numerical skills with the ability to use data to identify problems and support engineering decisions., • Proven planning, organisation and change‑management capability., • Excellent communication and people‑management skills, with the ability to work effectively across Engineering, Production, Quality and Supply Chain functions., • The ability to manage multiple priorities and remain effective within a demanding production environment. Experience in some of the following areas would be advantageous: • Medical devices or another highly regulated production environment., • ISO 13485 or comparable regulated quality systems., • Process validation and production validation., • Production line design, layout and optimisation., • Production tooling, jigs, fixtures and test equipment., • Lean Manufacturing, Six Sigma, SMED, 5S or related improvement methodologies., • Automation or semi‑automation of production processes., • Design for Manufacture and Assembly (DFMA)., • Supplier development and component qualification., • CAPA, 8D, root‑cause analysis or similar structured problem‑solving methodologies., • ERP/MRP and the effective use of production data. This appointment offers an unusual combination. You will be joining an established medical device business with an experienced workforce, respected products and a substantial engineering heritage, while also becoming part of a wider international medical technology group with significant ambitions for innovation, new products and production growth. For the right Production Engineering leader, this creates the opportunity to influence much more than the day‑to‑day running of an engineering department. You will have the opportunity to help determine how new products are introduced, how existing production processes evolve, which technologies and methods are adopted, and how the Abingdon operation prepares for its next phase of development. It is an opportunity for someone who enjoys making things better - combining the strengths of an established engineering business with the ideas, technologies and production strategies required for its future. #J-18808-Ljbffr

Oxford Nanopore Technologies is a global biotechnology company pioneering nanopore-based sensing technology that enables the analysis of DNA, RNA and other molecules. Our mission is to bring the widest benefits to society by enabling the analysis of anything, by anyone, anywhere! Headquartered in the UK and serving customers in over 125 countries, we are transforming scientific discovery and advancing research across human health, cancer, infectious diseases, agriculture and environmental science. We are looking for a Senior Production Quality Engineer to become our team's go-to production quality champion. In this role, you won't just be managing paperwork—you will be the bridge between Engineering, Production, and Supply Chain, driving root‑cause investigations, closing capability gaps, and embedding a proactive, gold‑standard quality culture across our entire production landscape. As Our Senior Production Quality Engineer, You Will Own The Quality Narrative On The Shop Floor And In The Lab. Your Day-to-day Will Involve: • Leading Investigations: Take full ownership of internal and supplier NCRs and CAPAs from initiation to verification, using structured root‑cause analysis (5‑Why, Fishbone, etc.)., • Standardising Excellence: Define, document, and standardise our goods‑in inspection processes, creating clear acceptance/rejection criteria and training the inspection teams to execute them flawlessly., • Mitigating Risk Early: Participate heavily in risk assessment activities (DFMEA/PFMEA) and review engineering drawings to ensure everything is clear, robust, and inspectable., • Driving Continuous Improvement: Analyse quality data to spot trends, eliminate systemic defects, and lead change control activities (including BOM and work instruction updates)., • Auditing & Compliance: Keep us sharp and audit‑ready, actively participating in internal and external audits (including ISO 13485). We need someone who understands the rigor of regulated manufacturing but possesses the soft skills to coach, mentor, and constructively challenge existing practices. • A degree in Mechanical Engineering (or a closely related discipline)., • Proven track record in a Quality Engineering or Manufacturing Quality role, ideally working with electromechanical devices., • Hands‑on working knowledge of ISO 13485 and ISO 14971., • Expertise in structured problem‑solving (CAPA/NCR management) and the ability to interpret engineering drawings and risk documentation., • A proactive, collaborative team player who can manage multiple moving parts, drive investigations forward, and work effectively in teams of 2 to 20 people., • A formal qualification in Quality or a Lean Six Sigma Green Belt., • An ISO 13485 Lead or Internal Auditor certification., • Experience specific to the medical device industry., • A knack for mentoring others and a strong grasp of statistical quality tools. This isn't a role where you will be an invisible cog in a massive machine. You will report directly to the Associate Director of Production Engineering, giving your work high visibility and real strategic weight. You will have the autonomy to build out processes, coach teams, and directly influence the reliability of life‑changing products. We offer outstanding benefits to include an attractive bonus, generous pension contributions, private healthcare and an excellent starting salary. If you are looking to utilise your skills to really make a difference to humankind, then consider joining our team and apply today! Please note that no terminology in this advert is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Every candidate will be assessed only in accordance with their merits, qualifications and abilities to perform the duties of the job. Our goal is to bring the widest benefits to society through enabling the analysis of anything, by anyone, anywhere. The company has developed a new generation of nanopore‑based sensing technology for faster, information‑rich, accessible and affordable molecular analysis. The first application is DNA/RNA sequencing, and the technology is in development for the analysis of other types of molecules including proteins. The technology is used to understand and characterise the biology of humans and diseases such as cancer, plants, animals, bacteria, viruses, and whole environments. With a thriving culture of ambition and strong innovation goals, Oxford Nanopore is a UK headquartered company with global operations and customers in more than 125 countries. #J-18808-Ljbffr

Caristo Diagnostics in Oxford, UK, is seeking a Software Developer Engineer in Test to strengthen its automation team. You will enhance a Python/Selenium/Behave framework, improve reliability and speed, and extend coverage across tests for medical device software validations. You will mentor juniors

Oxford, England, United Kingdom About IonQ: IonQ, Inc. [NYSE: IONQ] is the world’s leading quantum platform and merchant supplier - delivering integrated quantum solutions across computing, networking, sensing, and security. IonQ’s newest generation of quantum computers, the IonQ Tempo, is the latest in a line of cutting‑edge systems that have been helping customers and partners including Amazon Web Services, and AstraZeneca achieve 20x performance results and accelerate innovation in drug discovery, materials science, financial modeling, logistics, cybersecurity, and defense. In 2025, the company achieved 99.99% two-qubit gate fidelity, setting a world record in quantum computing performance. Headquartered in College Park, Maryland, IonQ has operations in California, Colorado, Massachusetts, Tennessee, Washington, Italy, South Korea, Sweden, Switzerland, Canada, and the United Kingdom. Our quantum computing services are available through all major cloud providers, while we also meet the needs of networking and sensing customers across land, sea, air, and space. IonQ is making quantum platforms more accessible and impactful than ever before. Location: Oxford, UK Office commitment: Hybrid The Role: Quantum is now, and it's built here. Oxford Ionics, now part of IonQ, is pioneering the next generation of quantum computing. Using our world‑leading trapped‑ion technology, we're building the most powerful, accurate and reliable quantum systems to tackle problems that today's supercomputers cannot solve. We're looking for an enthusiastic and highly technical Staff Software Engineer for our non‑realtime controllers team who will thrive in our dynamic cross‑disciplinary environment. You'd be working closely with our skilled software engineers, our systems teams who operate the physical quantum computers, and our world‑leading quantum scientists to build and operate the software that controls the hardware surrounding our quantum computers. Previous exposure to quantum systems is not required. You will take on our most demanding hardware integrations and the framework work that makes every other controller better. This is a hands‑on engineering role: you would be the most experienced engineer writing controllers, not the one directing others to write them. A working quantum computer is far more than the ion trap and its real‑time control electronics. It depends on a fleet of supporting hardware, including cryogenic compressors, vacuum pumps, power supplies, lasers, temperature controllers, wavemeters and cameras, that has to be kept observable, controllable and reliable. The timing‑critical operations such as gate waveforms and ion transport run on dedicated real‑time FPGA systems, while this team owns everything that does not need hard timing guarantees. These services run on general‑purpose Linux hardware and must be rock‑solid, because a failed compressor or an un‑noticed pressure drift takes a whole machine offline. Responsibilities: This is a hands‑on engineering role. Your influence comes from the code you ship and review, and from the problems you take off everyone other's plate. Key responsibilities include: • Take on our most demanding device integrations, and do the deep diagnosis of problems that only appear against real hardware in a live lab., • Remove whole classes of failure across the fleet, rather than instances of them., • Improve the shared framework yourself, and bring the existing controllers along with each change., • Build the tooling, simulators and test infrastructure that let the whole team move faster., • Evolve how our services are deployed and operated as the fleet grows, and make the fleet observable enough that problems are found early., • Raise the bar of everyone around you through the code you write and the reviews you give. Requirements: To be successful, you will need deep systems engineering experience, a track record of shipping and operating reliable services, and the judgement to tell a problem worth solving structurally from one worth patching. We're looking for someone who wants to stay hands‑on in the code at this level rather than move away from it. You’ll be a great fit with: • Expert systems engineering skills. Our controllers are written in Rust, so either solid Rust experience or deep proficiency in another systems language and the appetite to work in a Rust codebase, including async programming., • Experience building and operating networked services in production such as gRPC or REST, with a real grasp of error handling, observability and failure modes., • Experience of hardware and instrument protocols and interfaces such as SCPI, Modbus, serial and Ethernet., • A reputation as the person people bring the undiagnosable bug to, and the ability to prioritise work with a clear understanding of critical versus urgent items., • Excellent communication skills both within software and across disciplines. Be part of a team that’s shaping the future of quantum. We offer more than just a role, you’ll join a world class community of scientists, engineers and innovators working to unlock the full potential of quantum computing. We offer a range of benefits, including opportunities to further your career alongside industry leaders, a competitive salary with IonQ stock options, an annual performance bonus, generous annual leave, flexible hybrid working, private medical and dental insurance for you and your family, and much more. Join us and be part of the future of quantum computing. We’re proud to be an equal opportunity employer and welcome applicants from all backgrounds. Compensation will vary based on individual factors such as education, qualifications, and experience of the final candidate(s), specific office location, and calibration against relevant market data and internal team equity. Posted base salary figures are subject to change as new market data becomes available. Our benefits include comprehensive medical, dental, and vision plans, matching 401(k), unlimited PTO and paid holidays, parental/adoption leave, legal insurance, and a home technology stipend. Details of participation in these benefit plans will be provided when a candidate receives an offer of employment. At IonQ, we believe in fair treatment, access, opportunity, and advancement for all while striving to identify and eliminate barriers. We empower employees to thrive by fostering a culture of autonomy, productivity, and respect. We are dedicated to creating an environment where individuals can feel welcomed, respected, supported, and valued. We are committed to equity and justice. We welcome different voices and viewpoints and do not discriminate on the basis of race, religion, ancestry, physical and/or mental disability, medical condition, genetic information, marital status, sex, gender, gender identity, gender expression, transgender status, age, sexual orientation, military or veteran status, or any other basis protected by law. We are proud to be an Equal Employment Opportunity employer. US Technical Jobs. The position you are applying for will require access to technology that is subject to U.S. export control and government contract restrictions. Employment with IonQ is contingent on either verifying “U.S. Person” (e.g., U.S. citizen, U.S. national, U.S. permanent resident, or lawfully admitted into the U.S. as a refugee or granted asylum) status for export controls and government contracts work, obtaining any necessary license, and/or confirming the availability of a license exception under U.S. export controls. Please note that in the absence of confirming you are a U.S. Person for export control and government contracts work purposes, IonQ may choose not to apply for a license or decline to use a license exception (if available) for you to access export‑controlled technology that may require authorization, and similarly, you may not qualify for government contracts work that requires U.S. Persons, and IonQ may decline to proceed with your application on those bases alone. Accordingly, we will have some additional questions regarding your immigration status that will be used for export control and compliance purposes, and the answers will be reviewed by compliance personnel to ensure compliance with federal law. US Non-Technical Jobs. Due to applicable export control laws and regulations, candidates must be a U.S. citizen or national, U.S. permanent resident (i.e., current Green Card holder), or lawfully admitted into the U.S. as a refugee or granted asylum. Accordingly, we will have some additional questions regarding your immigration status that will be used for export control and compliance purposes, and the answers will be reviewed by compliance personnel to ensure compliance with federal law. #J-18808-Ljbffr

Employer Oxford University Hospitals NHS Foundation Trust Employer type NHS Site JR Hospital & Horton Hospital Town Oxford & Banbury Salary £49,387 - £56,515 per annum pro rata Salary period Yearly Closing 25/11/2026 23:59 Oxford University Hospitals NHS Foundation Trust is one of the largest NHS teaching trusts in the country. It provides a wide range of general and specialist clinical services and is a base for medical education, training and research. The Trust comprises of four hospitals - the John Radcliffe Hospital, Churchill Hospital and Nuffield Orthopaedic Centre in Headington and the Horton General Hospital in Banbury. Our values, standards and behaviours define the quality of clinical care we offer and the professional relationships we make with our patients, colleagues and the wider community. We call thisDelivering Compassionate Excellenceand its focus is on our values of compassion, respect, learning, delivery, improvement and excellence. Many of our recruitment programmes useValue Based Interviewingto identify those who have the skills we seek, who share our values and who are able to deliver compassionate excellence from the outset. We know that this makes a significant difference to your job satisfaction and above all the outcomes and experience of our patients and their families. For more information about our Values and Value Based Interviewing please visit www.ouh.nhs.uk/about/vision-and-values To undertake a range of diagnostic cardiac investigations at highly specialist cardiac physiologist level and provide expert, clinically accurate reports, adhering to local and national guidelines. Provide expert knowledge and skills in a range of cardiac investigations, communicating results across a multidisciplinary team. Provide training to all relevant members of the MDT in the delivery of routine and complex cardiac investigations. To work closely with the consultant cardiologists, clinical cardiac physiology leads, advanced nurse practitioners and other medical colleagues in providing clinical leadership and input into service development. To facilitate the efficient and effective management of resources within cardiac physiology. To contribute to the strategic development and daily operational management of the Department. To initiate and undertake audit within the specialist area and work collaboratively with research departments. To act as a clinical role model and resource to staff, and demonstrate a commitment to evidence based/best practice care and clinical excellence, in order to optimise quality of care. Ensure that the standards of the service delivered meet the national clinical standards and comply with the strategic aims of the Trust. The Oxford University Hospitals NHS Foundation Trust requires a clinically excellent BSE accredited Echocardiographer to join one of the largest NHS teaching trusts in the country. The Trust comprises of four hospitals, three in Oxford and one in Banbury and the Cardiac Physiology department works across all four sites and the rest of the county in community hubs. We are looking for a motivated Band 7 Cardiac Physiologist to join our supportive, dynamic, and friendly team. Candidates must be able to demonstrate post graduate level of working via a continuous development portfolio and evidence of leadership, mentorship and specialist working within an area of Cardiac Physiology would be advantageous. The successful post holder will join a large team of experienced Cardiac Physiologists, Arrhythmia and Complex Device Nurse Practitioners. The department encourages active involvement with professional bodies, and has regular representation at council level with BSE, BHRS and BCIS. We are a practical assessment centre for BSE and participate in the STP OSFA assessments for the National School of Healthcare Science. Professional development is encouraged at all levels. We are a National School of Healthcare Science accredited training centre. Professional registration is preferred i.e., RCCP or AHCS We would consider flexible working patterns. Oxford University Hospitals NHS Foundation Trustis one of the largest NHS teaching trusts in the country. It provides a wide range of general and specialist clinical services and is a base for medical education, training, and research. Find out more here www.ouh.nhs.uk The Trust comprises four hospitals - the John Radcliffe Hospital, Churchill Hospital and Nuffield Orthopaedic Centre in Headington and the Horton General Hospital in Banbury. Our values, standards and behaviours define the quality of clinical care we offer and the professional relationships we make with our patients, colleagues, and the wider community. We call thisDelivering Compassionate Excellenceand its focus is on our values of compassion, respect, learning, delivery, improvement and excellence. These values put patients at the heart of what we do and underpin the quality healthcare we would like for ourselves or a member of our family. Watch how we set out to deliver compassionate excellence via the OUH YouTube channel . • To support the Head of Cardiac Physiology in all operational/managerial matters as required e.g. effective use of resources, management of cardiac physiology personnel. · In collaboration with the Band 7 group create, support and develop a dynamic cardiac physiology team with a unified vision for future planning and development of the department. · To implement and support quality initiatives within Cardiac Medicine, in collaboration with the Band 7 group, by utilising effective use and monitoring of standards, auditing and evaluation of the echocardiography service in order to meet the needs of patients within this speciality. · To work with the Band 7 group to ensure procedures are in place to facilitate the achievement of Trust targets for cardiac medicine such as achieving diagnostic test waiting times and implementation of clinical governance frameworks. · In collaboration with the Head of Cardiac Physiology, lead the development and evaluation of relevant protocols, guidelines and procedures based on current evidence/research and facilitate /support other staff to do the same. · To monitor activity within the clinical area whilst ensuring that staffing levels and skill mix meet clinical requirements. · To promote awareness and understanding in others of efficient resource utilisation through education and example. · In collaboration with the Band 7 group to ensure that all new staff has an appropriate induction and orientation and assigned mentor. · To improve and develop Cardiac Physiologist roles Planned interview date: to be confirmed • • STP/ BSc Clinical Physiology or equivalent, • • Relevant experience performing at Band 6 level, • • Demonstrates ability to support junior and senior members of staff, • • Evidence of ongoing professional development, • • Evidence of leadership development, • • Recognised teaching /assessing qualification, • • Evidence of Masters level study, • • Demonstrable experience in a broad range of cardiac physiological procedures, such as ECG, Exercise Tolerance Testing supervision, Echocardiography, continuous ambulatory monitoring preparation and analysis, haemodynamic monitoring/recording during cardiac angiography & complex coronary intervention, implant and follow up of brady/tachy devices and Electrophysiological procedures., • • Experience in co-ordinating or managing a team, • • Professional attitude, takes pride in work, • • Patient centred approach, compassionate, • • Role model, open and honest in communication and delivers over and above what is expected, • • Respectful to colleagues and patients, respects diversity. Works well within a team, • • Committed to professional development of self and team, • • Ability to learn from successes and setbacks, • • Open to change, • • Effective communication skills (verbal and written, • • Demonstrates adaptability /flexibility and a positive approach to challenges, • • Able to cope under pressure, • • Decision making and problem solving skills, • • Professional appearance and compliance with policies, • • Ambitious and enthusiastic, • • Evidence of professional development Sexual Safety Charter : In 2023NHS England launched its first sexual safety charter, and our Trust proudly signed it. We pledge zero tolerance for inappropriate sexual behaviour and commit tothe ten core principles Oxford University Hospitalspromotes a safe, respectful hiring environment. Vacancy Closures: Please note, this vacancy may close early if a high volume of applications are received. Visa and Immigration: Oxford University Hospitals NHS Foundation Trust is able to offer Certificates of Sponsorship for all eligible roles for a Skilled Worker Visa without exception, provided the role meets the minimum salary and skill level criteria set by the Home Office (UKVI). All eligible candidates will be considered with equal consideration at all stages of the application and recruitment process. Skilled worker: Health and Care Visa | NHS Employers / Work in the UK - GOV.UK COVID-19: The COVID-19 vaccination remains the best way to protect yourself, your family, your colleagues and of course our patients from the virus when working in our healthcare settings. Whilst COVID-19 vaccination is not a condition of employment, we do encourage our staff to get vaccinated. If you are unvaccinated there is helpful advice and information at Oxfordshire County Council Website where you can also find out more about how to access vaccination. Probation Period: This post is subject to a 6 month probationary period. If you currently hold a contract of employment with the Oxford University Hospitals, this will not apply. This statement does not apply to Medical staff or Executive Appointments. Referencing: When providing employment reference details please provide correct work related email addresses so references can be sought promptly when we are looking to progress your application. Your first referee will need to be your line manager, supervisor or clinical lead from your current or most recent post or place of study. Please note that if you have previously worked for the Trust we will require a reference from your last Manager, this information is essential if your offer of employment is to be confirmed. To note: Applicants must write their own applications. If AI tools are used, the application may be rejected as this document is crucial for assessment. This does not prevent you from seeking support via AI with applications for the purposes of any disability and/or long-term health conditions. When using AI to help write your application, it is important to personalise it, especially your supporting statement. While AI can simplify the process, it will not fully understand the job's requirements and/or be able to showcase your skills, knowledge, and experience. Write your statement to show why you are interested in the role and how you would be a valued member of the team/OUH employee. No unsolicited recruitment agency telephone calls or emails. This post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service. Please note that this job advertisement will close automatically once the application limit is reached, regardless of whether this occurs before the advertised closing date. #J-18808-Ljbffr

Main area Electrophysiology (EP) Grade NHS Medical & Dental: Senior Clinical Fellow Contract Permanent: N/a Hours Full time - 40 hours per week (N/a) Job ref 321-MRC-MS-8271100-S6 Site Oxford University Foundation Trust Town Headington Salary £67,325 - £76,582 Per Annum Salary period Yearly Closing 16/11/2026 23:59 Oxford University Hospitals NHS Foundation Trust is one of the largest NHS teaching trusts in the country. It provides a wide range of general and specialist clinical services and is a base for medical education, training and research. The Trust comprises of four hospitals - the John Radcliffe Hospital, Churchill Hospital and Nuffield Orthopaedic Centre in Headington and the Horton General Hospital in Banbury. Our values, standards and behaviours define the quality of clinical care we offer and the professional relationships we make with our patients, colleagues and the wider community. We call thisDelivering Compassionate Excellenceand its focus is on our values of compassion, respect, learning, delivery, improvement and excellence. Many of our recruitment programmes useValue Based Interviewingto identify those who have the skills we seek, who share our values and who are able to deliver compassionate excellence from the outset. We know that this makes a significant difference to your job satisfaction and above all the outcomes and experience of our patients and their families. For more information about our Values and Value Based Interviewing please visit www.ouh.nhs.uk/about/vision-and-values This post is aimed at senior trainees in cardiac electrophysiology who already have experience in catheter ablation and cardiac device implantation who are within 6 months of their CCT. The job is primarily EP Lab-based with one clinic per week (and occasional extras) and specialist EP ward referral duties. The aim is to gain experience in complex ablation (e.g. atrial fibrillation, ventricular tachycardia), developing competence as a solo operator and prepare for a consultant role. • Responsibility for the care of adult patients undergoing investigation and treatment of heart rhythm conditions, • Day-to-day running of EP lab lists (patient consent and preparation, list coordination, discharge planning and administration), • Support of ablation and cardiac implantable device lists, • Autonomous “Fellow” EP lists in the lab, • Presentation and discussion of clinical cases at the multi-professional MDT, • Participation in research, governance and clinical audit within the unit., • Arrhythmia Clinic at OUH and occasionally associated hospitals., • Involvement in the training and supervision of junior medical staff in the EP lab, including the teaching of medical and nursing students. Oxford University Hospitals NHS Foundation Trust is one of the largest NHS teaching trusts in the country. It provides a wide range of general and specialist clinical services and is a base for medical education, training and research.The Trust comprises four hospitals - the John Radcliffe Hospital, Churchill Hospital and Nuffield Orthopaedic Centre in Headington and the Horton General Hospital in Banbury. Our values, standards and behaviours define the quality of clinical care we offer and the professional relationships we make with our patients, colleagues and the wider community. We call this Delivering Compassionate Excellence and its focus is on our values of compassion, respect, learning, delivery, improvement and excellence. These values put patients at the heart of what we do and underpin the quality healthcare we would like for ourselves or a member of our family. Watch how we set out to deliver compassionate excellence via the OUH YouTube channel . • Responsibility for the care of adult patients undergoing investigation and treatment of heart rhythm conditions, • Day-to-day running of EP lab lists (patient consent and preparation, list coordination, discharge planning and administration), • Support of ablation and cardiac implantable device lists, • Autonomous “Fellow” EP lists in the lab, • Presentation and discussion of clinical cases at the multi-professional MDT, • Participation in research, governance and clinical audit within the unit., • Arrhythmia Clinic at OUH and occasionally associated hospitals., • Involvement in the training and supervision of junior medical staff in the EP lab, including the teaching of medical and nursing students., • GMC Full Licence to Practice, • MRCP or equivalent, • General training in cardiology to registrar year 5 level or equivalent., • Experience in cardiac electrophysiology (a minimum of 12 months, • Within 6 months of CCT in Cardiology, • Experience in transseptal punctures (solo operator). Previous first-operatorexperience in pulmonary vein isolation ablation. Interest in research withpublications. CCT in Cardiology and Cardiac Electrophysiology, • experience in pulmonary vein isolation ablation. Interest in research withpublications., • experience in pulmonary vein isolation ablation. Interest in research withpublications. Sexual Safety Charter : In 2023NHS England launched its first sexual safety charter, and our Trust proudly signed it. We pledge zero tolerance for inappropriate sexual behaviour and commit tothe ten core principles Oxford University Hospital s promotes a safe, respectful hiring environment. If you want to make a difference with us, come and join our team. Together, we will uphold the highest standards of care and professionalism. Vacancy Closures: Please note, this vacancy may close early if a high volume of applications are received. Visa and Immigration: Oxford University Hospitals NHS Foundation Trust is able to offer Certificates of Sponsorship for all eligible roles for a Skilled Worker Visa without exception, provided the role meets the minimum salary and skill level criteria set by the Home Office (UKVI). All eligible candidates will be considered with equal consideration at all stages of the application and recruitment process. Skilled worker: Health and Care Visa | NHS Employers / Work in the UK - GOV.UK COVID-19: The COVID-19 vaccination remains the best way to protect yourself, your family, your colleagues and of course our patients from the virus when working in our healthcare settings. Whilst COVID-19 vaccination is not a condition of employment, we do encourage our staff to get vaccinated. If you are unvaccinated there is helpful advice and information at Oxfordshire County Council Website where you can also find out more about how to access vaccination. Probation Period: This post is subject to a 6 month probationary period. If you currently hold a contract of employment with the Oxford University Hospitals, this will not apply. This statement does not apply to Medical staff or Executive Appointments. Referencing: When providing employment reference details please provide correct work related email addresses so references can be sought promptly when we are looking to progress your application. Your first referee will need to be your line manager, supervisor or clinical lead from your current or most recent post or place of study. Please note that if you have previously worked for the Trust we will require a reference from your last Manager, this information is essential if your offer of employment is to be confirmed. To note: Applicants must write their own applications. If AI tools are used, the application may be rejected as this document is crucial for assessment. This does not prevent you from seeking support via AI with applications for the purposes of any disability and/or long-term health conditions. When using AI to help write your application, it is important to personalise it, especially your supporting statement. While AI can simplify the process, it will not fully understand the job's requirements and/or be able to showcase your skills, knowledge, and experience. Write your statement to show why you are interested in the role and how you would be a valued member of the team/OUH employee. No unsolicited recruitment agency telephone calls or emails. You must have appropriate UK professional registration. This post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service. Please note that this job advertisement will close automatically once the application limit is reached, regardless of whether this occurs before the advertised closing date. Band 5 NurseandBand 2 Healthcare Support Workerrecruitment iscentralised, meaning when you apply you will be considered fora number of rolesacross the Trust. If you have any questions please email: . Domestic / catering / porteringservices at theJohn Radcliffe Hospitalare provided byMitie. Domestic / catering / portering / maintenance engineerservices at theChurchill HospitalandNuffield Orthopaedic Centreare provided byG4S. Maintenance engineer services at the John Radcliffe Hospital are provided by Equans. To use ReachDeck to listen to or translate this site you must You can view our departments and services alphabetically. Some areas also have dedicated microsites, which are featured in the linked images below. "Oxford University" is a registered trade mark of the University of Oxford, and is used with the University's permission. #J-18808-Ljbffr

IonQ, Inc . [NYSE: IONQ] is the world's leading quantum platform and merchant supplier - delivering integrated quantum solutions across computing, networking, sensing, and security. IonQ's newest generation of quantum computers, the IonQ Tempo, is the latest in a line of cutting-edge systems that have been helping customers and partners including Amazon Web Services, and AstraZeneca achieve 20x performance results and accelerate innovation in drug discovery, materials science, financial modeling, logistics, cybersecurity, and defense. In 2025, the company achieved 99.99% two-qubit gate fidelity, setting a world record in quantum computing performance . This role is based at our Oxford, England (UK) office, with the option to work a few days a week remotely. Up to 5% 1765 We are looking for a Staff Analog Mixed-Signal Design and Modelling Engineer to join our Cryo-CMOS IC team at IonQ Oxford. In this role, you will develop behavioural models and mixed-signal verification environments for ASICs used in our trapped-ion quantum processors. In this position, you will build and maintain the model of the chip that the whole team simulates against, a mixed-abstraction model combining transistor-level circuits with Verilog-A/Verilog-AMS and SystemVerilog real-number behavioural blocks. These models will be derived form first-principles mathematics and correlated against schematic and measured silicon. You will decide which blocks are represented at which level of abstraction, keep the models faithful to the schematics and measured silicon. The full-chip model will then be used to verify the ASICs that control the quantum processor from room temperature down to a few kelvin. You will develop verification plans, run simulations and regressions, and validate models against circuit simulations and available silicon measurements. As a Staff Engineer, you will lead modelling and verification reviews, help define sign-off criteria and mentor other engineers. Your work will support tape-out and silicon bring-up, helping deliver reliable control electronics for IonQ's quantum computing systems. Key responsibilities include: • Own the full-chip modelling strategy: model architecture, abstraction levels, accuracy targets and sign-off criteria used across the IC development flow, • Owning analog and mixed-signal blocks (references, DACs, switches, regulators, clock distribution) from specification through schematic design, • Own top-level integration: define block interfaces and specifications, assemble the top level, and run the full-chip mixed-signal simulations that verify the ASIC Develop Verilog-A and Verilog-AMS models of analog blocks and assemble them into a simulatable full chip, • Build real-number models so the full chip runs in digital verification and regression at practical speed, • Derive models from mathematics: turn a transfer function, a Z-parameter network description or a MATLAB analysis into robust Verilog-A with well-behaved tolerances, • Define and run model-versus-schematic correlation, keeping models in sync with design releases, and feed measured silicon behaviour, back into the models and the block designs, • Develop verification plans from specifications, covering operating modes, analog-digital interfaces, power-up and reset sequences, and relevant process, voltage and temperature conditions., • Stand up mixed-signal co-simulation and regression (Cadence AMS Designer, Xcelium with Spectre) Lead block-level design reviews and mentor engineers on circuit design and modelling craft, • Lead modelling and verification reviews, define AMS sign-off criteria with the IC Lead, and present coverage, correlation results and risks for tape-out decisions, • Mentor engineers in modelling and verification To be successful, you will need deep analog and mixed-signal design and modelling experience, typically 10+ years. You will have designed blocks proven in silicon and models and used in production tape-out flows. You will bring expert transistor-level design of precision analog blocks (references, DACs, regulators, switches, clock distribution) taken through PVT and Monte Carlo, layout and silicon validation, together with expert Verilog-A and Verilog-AMS and strong real-number modelling. You'd be a great fit with: • Multiple tape-outs with responsibility for block design and top-level integration, including silicon bring-up and bench characterisation, • Strong mathematical foundations: linear systems, Laplace and z-domain analysis, network (Z-) parameters, noise and non-linearity, • Fluency in a production Cadence flow: Virtuoso, Spectre, Xcelium and AMS Designer or similar co-simulation environments, including parasitic extraction and post-layout sign-off, • SystemVerilog, plus MATLAB or Python/NumPy for analysis and model validation; scripting to automate model generation, checking and regression, • Cryogenic, space or other extreme-environment silicon experience will be highly beneficial, especially designing beyond foundry model validity using measured device data, • Ability to lead technical reviews, agree interfaces and verification criteria across teams, and communicate technical findings and risks clearly We're looking for someone who can design a block to specification and model it at the right fidelity, derive a model from equations and implement it end to end. You should be able to judge what to model and at what abstraction, align designers, verification and systems engineers on what a model does and does not promise, and contribute effectively within a fast-moving, highly technical team. Compensation will vary based on individual factors such as education, qualifications, and experience of the final candidate(s), specific office location, and calibration against relevant market data and internal team equity. Posted base salary figures are subject to change as new market data becomes available. Our benefits include comprehensive medical, dental, and vision plans, matching 401(k), unlimited PTO and paid holidays, parental/adoption leave, legal insurance, and a home technology stipend. Details of participation in these benefit plans will be provided when a candidate receives an offer of employment. At IonQ, we believe in fair treatment, access, opportunity, and advancement for all while striving to identify and eliminate barriers. We empower employees to thrive by fostering a culture of autonomy, productivity, and respect. We are dedicated to creating an environment where individuals can feel welcomed, respected, supported, and valued. We are committed to equity and justice. We welcome different voices and viewpoints and do not discriminate on the basis of race, religion, ancestry, physical and/or mental disability, medical condition, genetic information, marital status, sex, gender, gender identity, gender expression, transgender status, age, sexual orientation, military or veteran status, or any other basis protected by law. We are proud to be an Equal Employment Opportunity employer. The position you are applying for will require access to technology that is subject to U.S. export control and government contract restrictions. Employment with IonQ is contingent on either verifying "U.S. Person" (e.g., U.S. citizen, U.S. national, U.S. permanent resident, or lawfully admitted into the U.S. as a refugee or granted asylum) status for export controls and government contracts work, obtaining any necessary license, and/or confirming the availability of a license exception under U.S. export controls. Please note that in the absence of confirming you are a U.S. Person for export control and government contracts work purposes, IonQ may choose not to apply for a license or decline to use a license exception (if available) for you to access export-controlled technology that may require authorization, and similarly, you may not qualify for government contracts work that requires U.S. Persons, and IonQ may decline to proceed with your application on those bases alone. Accordingly, we will have some additional questions regarding your immigration status that will be used for export control and compliance purposes, and the answers will be reviewed by compliance personnel to ensure compliance with federal law. Due to applicable export control laws and regulations, candidates must be a U.S. citizen or national, U.S. permanent resident (i.e., current Green Card holder), or lawfully admitted into the U.S. as a refugee or granted asylum. Accordingly, we will have some additional questions regarding your immigration status that will be used for export control and compliance purposes, and the answers will be reviewed by compliance personnel to ensure compliance with federal law. #J-18808-Ljbffr

OrganOx is a commercial stage organ technology company dedicated to developing technologies to improve outcomes for patients with acute or chronic organ failure. The company was established as a spin out of the University of Oxford in 2008 and is now part of the Terumo Group. OrganOx is a pioneer in normothermic machine perfusion (NMP). It's flagship platform, the metra®, is available for use in the U.S., Europe, Canada, and Australia. It has been utilized in over 7,000 liver transplants to date to keep donor livers in a metabolically active state outside the body enabling longer preservation times and functional assessment of the organ prior to transplant, leading to an increased number of organs available for transplant. Founded in 1921, Terumo Corporation (TSE:4543) strives to fulfill its mission of "Contributing to Society through Healthcare" by providing a comprehensive range of solutions in the fields of therapeutic procedures, hospital operations, and life sciences in more than 160 countries and regions. OrganOx is a commercial stage organ technology company dedicated to developing technologies to improve outcomes for patients with acute or chronic organ failure. The company was established as a spin out of the University of Oxford in 2008 and is now part of the Terumo Group. OrganOx is a pioneer in normothermic machine perfusion (NMP). It's flagship platform, the metra®, is available for use in the U.S., Europe, Canada, and Australia. It has been utilized in over 7,000 liver transplants to date to keep donor livers in a metabolically active state outside the body enabling longer preservation times and functional assessment of the organ prior to transplant, leading to an increased number of organs available for transplant. Founded in 1921, Terumo Corporation (TSE:4543) strives to fulfill its mission of "Contributing to Society through Healthcare" by providing a comprehensive range of solutions in the fields of therapeutic procedures, hospital operations, and life sciences in more than 160 countries and regions. The Senior Electronics Design Engineer will take a leading role in the design, development, and verification of electronic systems for OrganOx medical devices. This role combines hands-on electronics design with technical ownership of subsystems, supporting architectural decisions and mentoring less-experienced engineers. This is an on-site role in Oxford with flexibility, combining on-site collaboration with remote design work to ensure close interaction with cross-functional engineering, quality, and regulatory teams. • Owning the design and development of electronic subsystems from concept through to manufacturing handover, • Designing analogue, digital, and mixed-signal circuits with a strong focus on safety, reliability, and compliance, • Producing and reviewing schematics and PCB layouts, ideally using Altium Designer, • Supporting electronic architecture decisions in collaboration with the Principal Electronics Engineer, Software engineering and systems engineering, • Performing component selection, design calculations, and risk assessments in line with IEC 60601 and ISO 14971, • Leading electronics design verification activities, including functional testing, EMC pre-compliance, and safety-related testing, • Supporting debugging and root-cause analysis during prototype development and verification, • Preparing and maintaining high-quality technical documentation suitable for regulated medical device development, • Supporting transfer to manufacturing, including engagement with suppliers and CMOs, • Providing technical guidance and informal mentoring to junior electronics engineers, • Participating actively in design reviews and contributing to continuous product improvement, • Adhere to the letter and spirit of OrganOx's Code of Conduct and all other company policies, • Proven relevant industry experience in electronics design, • Strong experience in analogue and digital electronics design for complex products, • Experience in safety-critical, regulated industries, preferably medical devices, is strongly preferred, • Proven ability to take ownership of electronic subsystems and deliver them to production, • Proficiency in schematic capture and PCB layout; experience with Altium Designer is highly desirable, • Good understanding of EMC/EMI mitigation techniques and design-for-manufacture principles, • Hands-on experience with laboratory test equipment (oscilloscopes, logic analysers, spectrum analysers), • Working knowledge of medical device standards (IEC 60601, ISO 13485, IEC 62304, ISO 14971) would be an advantage, • Ability to work independently while collaborating effectively within a multidisciplinary team, • Clear communication skills, including the ability to explain technical decisions and trade-offs, • Ability to travel occasionally (up to 10%), • Bachelor's or Master's degree in Electronics Engineering or a related discipline At OrganOx, we value innovation, evidence, integrity, teamwork, respect, and passion. We offer competitive compensation and comprehensive benefits, including healthcare and retirement plans. We support work-life balance and provide opportunities for ongoing professional development. We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to age, disability, gender reassignment, marriage and civil partnership, pregnancy and maternity, race, religion or belief, sex, sexual orientation race, or any other characteristics protected by law. #J-18808-Ljbffr

At the Ellison Institute of Technology (EIT), we’re on a mission to translate scientific discovery into real world impact. We bring together visionaryscientists, technologists, engineers, researchers, educators and innovatorsto tackle humanity’s greatest challenges in four transformative areas: • Health, Medical Science & Generative Biology, • Food Security & Sustainable Agriculture, • Climate Change & Managing CO₂, • Artificial Intelligence & Robotics This is ambitious work - work that demands curiosity, courage, and a relentless drive to make a difference. At EIT, you’ll join a community built on excellence, innovation, tenacity, trust, and collaboration, where bold ideas become real-world breakthroughs. Together, we push boundaries, embrace complexity, and create solutions to scale ideas from lab to society. Explore more at www.eit.org. The Scientific Compute and Data team builds the compute, data and tooling foundation behind EIT's science. We run the cloud and GPU infrastructure that the models train on, the data infrastructure that instruments, robots and researchers use, and the data products and shared data models that let one team's results be built on by the next. We provide hands-on expertise in platform engineering, data engineering, and data management, and create common tooling for every lab to accelerate their experiments across gene editing, battery chemistry, plant biology and more. At EIT we are seeking an experienced Data Engineer to join our Scientific Compute and Data team. Our Data Engineers in Autonomous Systems work within a wider project, AutoLabs. This is where EIT automates the scientific discovery loop: experimental design, execution, analysis, and the learning that feeds back into the next experiment and the lab itself. The AutoLabs data platform captures, stores and serves high-frequency multimodal data. It spans an edge-to-cloud telemetry stack (MQTT, Kafka, media streams such as HLS), streaming APIs, and a growing set of hardware integrations across multiple sites including robotic systems, sensor rigs and lab instruments. Our labs produce raw data for a fast-growing set of models: vision-language-action models, orchestration and monitoring models, and world models that learn the dynamics of a laboratory to simulate experiments before they are run. As a Data Engineer, you’ll work directly alongside AI researchers, software engineers, robotics engineers, and domain scientists to build the data layer that makes our autonomous operations possible. You will contribute to an engineering culture that values robust system design, testing, and deep collaboration, but allows flexibility for rapid prototyping and responsiveness to changing landscapes. • Build high-throughput, low-latency ingestion for live video, sensor telemetry, robot joint state and instrument control signals, integrating validation at the edge before data reaches the cloud., • Work across the edge-to-cloud stack, from edge devices and MQTT brokers through to Kafka topics, cloud storage, and the APIs that serve scientists and ML pipelines., • Turn streams of robot state, instrument output and video into structured database transactions: which arm did what to which sample, when, and what came out., • Build the knowledge graph on top of that, linking inputs to results, so that a fact can always be traced back to the video segment and sensor readings behind it., • Make the output model-ready: the formats, sampling, labelling and provenance that training and evaluation need, working directly with the researchers who consume it.Nobody checks every box - if you’re not sure if you’re qualified, we still encourage you to apply., • You have strong programming experience in Python, and value code quality, reliability, and performance while adapting to an evolving industry., • You think in systems and own them end-to-end - from device output to APIs - and embrace long-term engineering rather than one-off scripts., • Experience with real-time data streaming - Kafka or Pub/Sub (or equivalent), and the challenges that come with high-frequency, low-latency data capture., • You treat reproducibility, version control, schema design and lineage as the things that make good science possible., • A clear, respectful communicator who can collaborate with scientists, roboticists and researchers., • Automated lab or life sciences environments - instrument APIs, lab protocols, and what scientists expect of data quality., • Data pipelines for physical systems: robotics (e.g. MQTT), autonomous vehicles, lab or clinical instruments, industrial control, or similar environments., • Knowledge, entity, search or feed systems where correctness under continuous update was the hard part., • Stateful stream processing (Flink, Kafka Streams, Beam or similar): event time, watermarks, exactly-once., • APIs for data ingestion and consumption with FastAPI, gRPC or GraphQL., • Graph stores and entity resolution or curation at scale, where the interesting decisions are about what to keep, merge or drop., • Experience working close to model development, such as curating training or evaluation data, or building the data systems that feed models. You don’t need to be a machine learning engineer, but you should know what makes a dataset good., • Salary dependent on experience + travel allowance + bonus, • Enhanced holiday. Our annual leave allowance is 25 days plus 8 bank holidays and an additional 3 days between Christmas and New Year. You will also have the opportunity to purchase an additional 5 days annual leave in January and July., • Pension - Employer contribution 7.5%, minimum employee contribution 5%, • Life Assurance., • Income Protection, • Private Medical Insurance as standard for you, your partner and any dependents. Including hospital Cash Plan, • Employee discounts, • Electric car scheme, • Nursery Salary Sacrifice scheme, • Cycle to Work Scheme, • Family Planning, • Neurodiversity support including advise and assessments, • Coaching & Therapy services, • 2 days per week in Oxford office, 1 day per week in employee’s choice of Oxford or London office, 2 days per week work from any UK location., • You must have the right to work permanently in the UK with a willingness to travel as necessary. In certain cases, we can consider sponsorship, and this will be assessed on a case-by-case basis. #J-18808-Ljbffr

OrganOx is seeking a Principal Electronics Engineer to serve as the technical lead for electronics design across OrganOx products. This on-site role in Oxford combines hands-on design, technical leadership, and mentoring of junior engineers to deliver robust, compliant electronic solutions. The role collaborates with engineering, quality, and regulatory teams to ensure designs meet stringent medical device standards and are suitable for high-volume manufacturing. #J-18808-Ljbffr

Role: Principal FPGA Design Engineer Location: Oxfordshire Package: £80k - £120k + Bonus + Generous Benefits About the Business: We are partnering with a pioneering UK technology innovator developing next-generation medical device technologies. Operating globally, they combine hardware, custom silicon, and complex data processing to transform global healthcare and scientific research. Role Overview: A hands-on technical leadership and mentorship position, owning the architecture and delivery of high-throughput FPGA subsystems. You will drive designs across the full lifecycle-from initial requirements through RTL implementation, custom-ASIC bring-up, lab validation, and product release. Key Responsibilities: • System Architecture: Lead FPGA subsystem architecture for complex data platforms., • RTL & Verification: Design/verify digital RTL (SystemVerilog/Verilog) using AMD/Xilinx toolchains., • Optimization: Maximize throughput, power efficiency, resource usage, and timing closure., • Integration: Collaborate with ASIC, FW, and SW teams to support board bring-up., • Leadership: Champion CI/CD automation and mentor mid/senior hardware engineers. What We Need: • Proven full-lifecycle FPGA design experience (architecture to hardware bring-up)., • Strong SystemVerilog/Verilog skills with AMD/Xilinx toolchains (Vivado/Questa)., • Hands-on experience with high-speed interfaces (PCIe/DMA) and lab debugging tools., • Scripting for workflow automation (Python, Tcl, Make)., • Degree in Electronic Engineering or equivalent industry background. Apply: Interested in leading core architecture on high-impact technology? Apply with your CV today for a confidential discussion.

Metric Bio are proud to continue supporting one of our longest-standing partners, a pioneering medical device company whose technology is directly saving lives. Their platform has already been used in over 7,000 life‑critical transplant procedures worldwide. Backed by a global healthcare leader and spun out of a world‑renowned UK university, this is a rare opportunity to build software that genuinely matters. They are looking for a Windows Software Engineer to join a close‑knit engineering team in Oxford, contributing across the full SDLC with a focus on device hosted applications, product connectivity and robust cybersecurity in a regulated medical device environment. • Designing and developing software for a Class II/III medical device in compliance with IEC 62304, ISO 14971, IEC 62366 and FDA regulations, • Owning requirements definition, design documentation and comprehensive traceability across all phases of design control, • Implementing multi‑threading, asynchronous programming and deterministic behaviour in device environments, • Building and maintaining secure connectivity using TLS, certificate based authentication and messaging technologies such as Azure IoT Hub and MQTT, • Designing OTA update mechanisms including safe rollback, validation and compatibility strategies, • Contributing to hazard analysis, FMEA, code reviews, unit testing and integration testing, • Collaborating with Electronics, Systems, Data Science, QARA and Field Service teams across product engineering and new product development, • Expert level C# and modern .NET (versions 6, 7 or 8) in long‑lived production systems, along with PowerShell scripting, • Proven experience developing device hosted applications and services on Windows based platforms, • Strong knowledge of Windows security hardening and cybersecurity best practices, • Experience with dependency injection, application lifecycle management and structured logging tools such as Serilog or NLog, • Familiarity with requirements management tools such as Codebeamer, Polarion or Jama, and task management via Jira, • A track record of delivering to IEC 62304 or an equivalent regulated framework, ideally in medical devices, • Degree in Computer Science or a relevant engineering discipline Apply if you want to use your technical skills to genuinely positively impact human lives! #J-18808-Ljbffr

Planet Recruitment seeks a Technical Publications Administrator in Abingdon to turn complex mechanical and electronic information into practical instructions.You will create and maintain IFUs, service manuals, and production procedures for medical devices, with a strong focus on accuracy and clear c

At the Ellison Institute of Technology (EIT), we’re on a mission to translate scientific discovery into real world impact. We bring together visionaryscientists, technologists, engineers, researchers, educators and innovatorsto tackle humanity’s greatest challenges in four transformative areas: • Health, Medical Science & Generative Biology, • Food Security & Sustainable Agriculture, • Climate Change & Managing CO₂, • Artificial Intelligence & Robotics This is ambitious work - work that demands curiosity, courage, and a relentless drive to make a difference. At EIT, you’ll join a community built on excellence, innovation, tenacity, trust, and collaboration, where bold ideas become real-world breakthroughs. Together, we push boundaries, embrace complexity, and create solutions to scale ideas from lab to society. Explore more at . Within this ecosystem, the Pathogen Mission exemplifies EIT’s commitment to transformative science. It aims to revolutionise the diagnosis and treatment of infectious diseases by leveraging whole genome sequencing (WGS)-based metagenomic and pathogen-specific analytical tools. This remit includes the development of a decentralised, sample-to-answer sequencing diagnostic platform for infectious diseases, enabling rapid and accurate analysis of patient samples without prior assumptions. Supported by Oracle Inc.’s cloud-computing scale and security infrastructure, the Pathogen Mission is progressing towards certified diagnostic products for deployment in laboratories, hospitals, and public health organisations worldwide. We’re seeking an experienced and innovative Senior MEMS Development Engineer to develop novel microfabricated devices and sensor interfaces for next-generation nanopore sequencing technologies. This hands-on role will focus on designing, prototyping, and characterising MEMS devices, taking concepts from proof-of-concept through to integrated multi-channel sensing systems. Working closely with a Senior Electronics R&D Engineer, you’ll drive device development through iterative design, testing, and optimisation. You’ll tackle challenges spanning microfabrication, materials, device architecture, and MEMS‑electronics integration while collaborating with external fabrication partners and technical suppliers. As the programme grows, you’ll help establish the MEMS engineering capabilities, processes, and technical foundations needed to support a wider multidisciplinary team. • Take technical ownership of the MEMS engineering development of novel microfabricated sensing structures and device interfaces, from early concepts through to functional prototypes and integrated systems., • Design and develop microfabricated devices and test structures, including the selection of materials, fabrication processes and device geometries., • Develop and evaluate fabrication approaches using established semiconductor and MEMS manufacturing techniques, adapting processes to meet the requirements of novel sensing devices., • Work closely with the Senior Electrical R&D Engineer to co-develop and evaluate prototype devices, using experimental findings to guide iterative improvements in MEMS design and electronic integration., • Design and characterise mechanical, electrical and material interfaces, investigating their influence on device performance, reliability and repeatability., • Develop experimental methods and test structures to assess fabrication quality, dimensional accuracy, device performance and reliability., • Investigate the effects of materials, surface properties, fabrication tolerances and assembly processes on device behaviour and performance., • Collaborate with electrical and mechanical engineers to develop prototype assemblies, alignment methods and experimental test platforms., • Identify and resolve fabrication challenges through design iteration, experimental characterisation and failure analysis., • Develop increasingly sophisticated prototype devices as the project progresses, supporting the transition from initial feasibility studies to integrated nanopore sensing systems., • Identify and engage specialist external fabrication facilities, engineering suppliers and technical collaborators to support the development and manufacture of prototype components and devices., • Define technical specifications and fabrication requirements for external suppliers, including design documentation, material requirements, dimensional tolerances and performance criteria., • Coordinate technical activities with external suppliers and collaborators, reviewing fabrication approaches, monitoring progress and evaluating deliverables against agreed requirements., • Plan and execute structured experiments, analyse performance data and translate findings into engineering requirements and design improvements., • Contribute to the selection and development of fabrication methods, considering manufacturability, scalability, cost and process reliability., • Maintain clear technical documentation, design records and experimental results, contributing to intellectual property development and technical reviews while ensuring appropriate confidentiality., • Provide technical guidance and mentoring as the engineering team expands, helping establish robust engineering practices and development processes. We welcome applicants from industry, applied research and academia who can demonstrate strong technical expertise and practical engineering capability. • Degree in Electrical Engineering, Mechanical Engineering, Materials Science, Physics or a related discipline, or equivalent relevant experience., • Significant experience in MEMS engineering, semiconductor microfabrication or microdevice development, ideally involving novel sensors, electronic interfaces or precision microfabricated systems., • Strong understanding of MEMS design principles, materials selection and microfabrication techniques., • Experience designing microfabricated devices using CAD tools, including the preparation of layouts, fabrication drawings or photolithography mask designs., • Practical knowledge of semiconductor and MEMS manufacturing processes, such as photolithography, thin-film deposition, etching, surface treatment and metallisation., • Experience developing and characterising prototype devices, including dimensional, mechanical and electrical evaluation., • Ability to understand and resolve fabrication challenges through experimental investigation, design modification and process optimisation., • Knowledge of material properties, fabrication tolerances and their influence on device functionality and reliability., • Experience planning and executing structured experimental programmes to characterise complex devices and resolve technical challenges., • Ability to work independently, establish technical approaches and deliver functional prototypes in an early-stage R&D environment., • Experience collaborating with multidisciplinary teams and translating requirements between MEMS, electronics, mechanical engineering and device fabrication., • Ability to develop clear technical specifications and work effectively with external fabrication facilities, engineering suppliers or development partners., • Experience developing MEMS or microfabricated devices for biosensing, electrochemical sensing, nanopore technologies or other sensor applications., • Knowledge of silicon micromachining, wafer processing and microelectronic device fabrication., • Experience with microfabricated electrodes, conductive thin films, dielectric materials or electronic sensor interfaces., • Familiarity with microelectronic packaging, device assembly, bonding and integration of MEMS with electronic systems., • Experience with polymeric materials, elastomeric components or other compliant materials used in microsystems., • Knowledge of mechanical contact behaviour, surface interactions, material deformation and reliability testing at small length scales., • Experience with optical microscopy, electron microscopy, profilometry, surface analysis or other microdevice characterisation techniques., • Experience designing devices that incorporate fluidic, electrochemical or biological components., • Familiarity with finite element analysis or other simulation methods for mechanical, thermal or material behaviour., • Experience working with external MEMS foundries, academic cleanroom facilities or specialist microfabrication suppliers., • Knowledge of fabrication process development, process yield improvement and quality control., • Understanding of design for manufacture, engineering reliability and transitioning prototype devices towards scalable production., • Hands-on and inventive: Enjoys solving technical challenges through practical engineering, experimentation and rapid prototyping., • Comfortable with early-stage R&D: Able to work effectively where solutions are not yet established and technical requirements evolve through experimentation., • Analytical and systematic: Uses sound engineering judgement and quantitative evidence to understand complex behaviour and guide design decisions., • Collaborative: Works closely with specialists in electronics, mechanical engineering, chemistry and MEMS fabrication, as well as external technical partners, to develop integrated solutions., • Independent and proactive: Can establish experimental capabilities, identify priorities and progress technical work with limited existing infrastructure., • Technically ambitious: Motivated by challenging engineering problems and developing technologies with the potential for substantial real-world impact., • Clear communicator: Able to explain complex technical challenges, document findings and communicate requirements effectively with colleagues, suppliers and external collaborators., • Salary: Competitive + travel allowance + bonus, • Enhanced holiday pay, • Pension, • Life Assurance, • Income Protection, • Private Medical Insurance, • Hospital Cash Plan, • Therapy Services, • Perk Box, • Electric Car Scheme, • You must have the right to work permanently in the UK with a willingness to travel as necessary. In certain cases, we can consider sponsorship, and this will be assessed on a case-by-case basis., • You will live in, or within easy commuting distance of, Oxford (or be willing to relocate)., • You must be eligible to work in the UK with occasional travel (1-3 trips per year). #J-18808-Ljbffr

Oxford Ionics, now part of IonQ, is pioneering the next generation of quantum computing. Using our world-leading trapped-ion technology, we’re building the most powerful, accurate and reliable quantum systems to tackle problems that today’s supercomputers cannot solve. Joining Oxford Ionics means becoming part of a global IonQ team that is transforming the future of quantum technology - faster, at scale, and with real world impact. IonQ, Inc. [NYSE: IONQ] is the world’s leading quantum company delivering solutions to solve the world’s most complex problems. IonQ’s newest generation quantum computers, IonQ Tempo and IonQ Forte Enterprise, are the latest in cutting-edge systems that have been helping customers and partners such as Amazon Web Services, AstraZeneca, and NVIDIA achieve 20x performance results. The company achieved 99.99% two-qubit gate fidelity, setting a world record in quantum computing performance in 2025. The company is accelerating its technology roadmap and intends to deliver the world’s most powerful quantum computers with 2 million qubits by 2030 to accelerate innovation in drug discovery, materials science, financial modeling, logistics, cybersecurity, and defense. IonQ’s advancements in quantum networking position the company as a leader in building the quantum internet. We’re looking for a Senior Photonics Test Engineer to join our photonics effort and own the experimental characterisation and validation of photonic devices and components that support our quantum computing platform. This is a lab-first, hands-on metrology role: you’ll design and operate optical test setups (often microscope-style systems with stages, alignment, and calibration) that generate trusted data and clear pass/fail decisions on device performance. You’ll sit close to the action; working day-to-day with photonics, device, and hardware teams. Turning real measurements into feedback that improves designs and accelerates iteration. If you like building robust measurement rigs, tightening repeatability, and making experimental data genuinely useful, this one’s for you. You’ll take ownership of testing, characterising, and validating photonic components and devices, and you’ll help raise the bar on how we design and run metrology in the lab. This role blends practical optical engineering with strong experimental discipline: selecting components, designing measurement approaches, running experiments, and turning results into clear technical direction for the wider team. Responsibilities include: • Device characterisation: Run experimental testing and characterisation of photonic devices/components using advanced optical equipment, producing clear, defensible results., • Metrology setup design: Design, assemble, validate and calibrate optical measurement setups to improve capability, throughput, and repeatability., • Data + reporting: Analyse and interpret experimental data, presenting insights to stakeholders and guiding performance optimisation., • Cross-functional collaboration: Work closely with engineers and scientists across the stack to translate measurement outcomes into next-step design and test priorities. You’ll be someone who’s genuinely happy spending most of your time in the lab, building and operating optical test rigs and treating measurement quality (calibration, repeatability, documentation) as a craft. You don’t need to be the world’s leading integrated photonics expert but you do need strong optics fundamentals, a track record in metrology / characterisation, and the ability to take a setup from “idea” to “trusted tool” that the team can rely on. Bonus points if you’ve automated acquisition/analysis pipelines and improved measurement throughput in previous roles. • Strong experience with optical metrology / component characterisation in a hands-on lab environment., • Proven ability to design, assemble and calibrate optical test equipment or microscope-style measurement setups., • Confidence with data analysis and turning results into clear technical recommendations (automation skills a plus)., • A collaborative mindset—comfortable working across teams and communicating experimental outcomes clearly. So why us? Be part of a team that’s shaping the future of quantum. We offer more than just a role, you’ll join a world class community of scientists, engineers and innovators working to unlock the full potential of quantum computing. We offer a range of benefits, including opportunities to further your career alongside industry leaders, a competitive salary with IonQ stock options, an annual performance bonus, generous annual leave, flexible hybrid working, private medical and dental insurance for you and your family, and much more. Join us and be part of the future of quantum computing. We’re proud to be an equal opportunity employer and welcome applicants from all backgrounds. #J-18808-Ljbffr

• Responsibility for the care of adult patients undergoing investigation and treatment of heart rhythm conditions, • Day-to-day running of EP lab lists (patient consent and preparation, list coordination, discharge planning and administration), • Support of ablation and cardiac implantable device lists, • Autonomous "Fellow" EP lists in the lab, • Presentation and discussion of clinical cases at the multi-professional MDT, • Participation in research, governance and clinical audit within the unit., • Arrhythmia Clinic at OUH and occasionally associated hospitals., • Involvement in the training and supervision of junior medical staff in the EP lab, including the teaching of medical and nursing students. GMC Full Licence to Practice • MRCP or equivalent, General training in cardiology to registrar year 5 level or equivalent., • Experience in cardiac electrophysiology (a minimum of 12 months, • Within 6 months of CCT in Cardiology, • Experience in transseptal punctures (solo operator). Previous first-operatorexperience in pulmonary vein isolation ablation. Interest in research withpublications. CCT in Cardiology and Cardiac Electrophysiology, • experience in pulmonary vein isolation ablation. Interest in research withpublications., experience in pulmonary vein isolation ablation. Interest in research withpublications. In 2023 NHS England launched its first sexual safety charter, and our Trust proudly signed it. We pledge zero tolerance for inappropriate sexual behaviour and commit to the ten core principles, You must have appropriate UK professional registration. Oxford University Hospitals NHS Foundation Trust is one of the largest NHS teaching trusts in the country. It provides a wide range of general and specialist clinical services and is a base for medical education, training and research. The Trust comprises of four hospitals - the John Radcliffe Hospital, Churchill Hospital and Nuffield Orthopaedic Centre in Headington and the Horton General Hospital in Banbury. Our values, standards and behaviours define the quality of clinical care we offer and the professional relationships we make with our patients, colleagues and the wider community. We call this Delivering Compassionate Excellence and its focus is on our values of compassion, respect, learning, delivery, improvement and excellence. Oxford University Hospitals NHS Foundation Trust is one of the largest NHS teaching trusts in the country. It provides a wide range of general and specialist clinical services and is a base for medical education, training and research.The Trust comprises four hospitals - the John Radcliffe Hospital, Churchill Hospital and Nuffield Orthopaedic Centre in Headington and the Horton General Hospital in Banbury. Our values, standards and behaviours define the quality clinical care we offer and the professional relationships we make with our patients, colleagues and the wider community. We call this Delivering Compassionate Excellence and its focus is on our values of compassion, respect, learning, delivery, improvement and excellence. These values put patients at the heart of what we do and underpin the quality healthcare we would like for ourselves or a member of our family. Watch how we set out to deliver compassionate excellence via the OUH YouTube channel. Oxford University Hospitals promotes a safe, respectful hiring environment. If you want to make a difference with us, come and join our team. Together, we will uphold the highest standards of care and professionalism. #J-18808-Ljbffr

Company: Company: Oxford University Hospitals NHS Foundation Trust This post is aimed at senior trainees in cardiac electrophysiology who already have experience in catheter ablation and cardiac device implantation who are within 6 months of their CCT. The job is primarily EP Lab-based with one clinic per week (and occasional extras) and specialist EP ward referral duties. The aim is to gain experience in complex ablation (e.g. atrial fibrillation, ventricular tachycardia), developing competence as a solo operator and prepare for a consultant role. • Responsibility for the care of adult patientsundergoing investigation and treatment of heart rhythm conditions, • Day-to-day running of EP lab lists (patient consent and preparation, list coordination, discharge planning and administration), • Support of ablation and cardiac implantable device lists, • Autonomous “Fellow” EP lists in the lab, • Presentation and discussion of clinical cases at the multi-professional MDT, • Participation in research, governance and clinical audit within the unit., • Arrhythmia Clinic at OUH and occasionally associated hospitals., • Involvement in the training and supervision of junior medical staff in the EP lab, including the teaching of medical and nursing students. Oxford University Hospitals NHS Foundation Trustis one of the largest NHS teaching trusts in the country. It provides a wide range of general and specialist clinical services and is a base for medical education, training and research.The Trust comprises four hospitals - the John Radcliffe Hospital, Churchill Hospital and Nuffield Orthopaedic Centre in Headington and the Horton General Hospital in Banbury. Our values, standards and behaviours define the quality of clinical care we offer and the professional relationships we make with our patients, colleagues and the wider community. We call this Delivering Compassionate Excellence and its focus is on our values of compassion, respect, learning, delivery, improvement and excellence. These values put patients at the heart of what we do and underpin the quality healthcare we would like for ourselves or a member of our family. Watch how we set out to deliver compassionate excellence via theOUH YouTube channel. • Responsibility for the care of adult patientsundergoing investigation and treatment of heart rhythm conditions, • Day-to-day running of EP lab lists (patient consent and preparation, list coordination, discharge planning and administration), • Support of ablation and cardiac implantable device lists, • Autonomous “Fellow” EP lists in the lab, • Presentation and discussion of clinical cases at the multi-professional MDT, • Participation in research, governance and clinical audit within the unit., • Arrhythmia Clinic at OUH and occasionally associated hospitals., • Involvement in the training and supervision of junior medical staff in the EP lab, including the teaching of medical and nursing students. This advert closes on Monday 16 Nov 2026 #J-18808-Ljbffr

Main area Cardiac Physiology Grade Band 7 Contract Permanent: 4 day week Hours • Full time, • Part time, • Flexible working37.5 hours per week Job ref 321-MRC-8298119-B7 Site JR Hospital & Horton Hospital Town Oxford & Banbury Salary £49,387 - £56,515 per annum pro rata Salary period Yearly Closing 25/11/2026 23:59 Oxford University Hospitals NHS Foundation Trust is one of the largest NHS teaching trusts in the country. It provides a wide range of general and specialist clinical services and is a base for medical education, training and research. The Trust comprises of four hospitals - the John Radcliffe Hospital, Churchill Hospital and Nuffield Orthopaedic Centre in Headington and the Horton General Hospital in Banbury. Our values, standards and behaviours define the quality of clinical care we offer and the professional relationships we make with our patients, colleagues and the wider community. We call thisDelivering Compassionate Excellenceand its focus is on our values of compassion, respect, learning, delivery, improvement and excellence. Many of our recruitment programmes useValue Based Interviewingto identify those who have the skills we seek, who share our values and who are able to deliver compassionate excellence from the outset. We know that this makes a significant difference to your job satisfaction and above all the outcomes and experience of our patients and their families. For more information about our Values and Value Based Interviewing please visit www.ouh.nhs.uk/about/vision-and-values To undertake a range of diagnostic cardiac investigations at highly specialist cardiac physiologist level and provide expert, clinically accurate reports, adhering to local and national guidelines. Provide expert knowledge and skills in a range of cardiac investigations, communicating results across a multidisciplinary team. Provide training to all relevant members of the MDT in the delivery of routine and complex cardiac investigations. To work closely with the consultant cardiologists, clinical cardiac physiology leads, advanced nurse practitioners and other medical colleagues in providing clinical leadership and input into service development. To facilitate the efficient and effective management of resources within cardiac physiology. To contribute to the strategic development and daily operational management of the Department. To initiate and undertake audit within the specialist area and work collaboratively with research departments. To act as a clinical role model and resource to staff, and demonstrate a commitment to evidence based/best practice care and clinical excellence, in order to optimise quality of care. Ensure that the standards of the service delivered meet the national clinical standards and comply with the strategic aims of the Trust. The Oxford University Hospitals NHS Foundation Trust requires a clinically excellent BSE accredited Echocardiographer to join one of the largest NHS teaching trusts in the country. The Trust comprises of four hospitals, three in Oxford and one in Banbury and the Cardiac Physiology department works across all four sites and the rest of the county in community hubs. We are looking for a motivated Band 7 Cardiac Physiologist to join our supportive, dynamic, and friendly team. Candidates must be able to demonstrate post graduate level of working via a continuous development portfolio and evidence of leadership, mentorship and specialist working within an area of Cardiac Physiology would be advantageous. The successful post holder will join a large team of experienced Cardiac Physiologists, Arrhythmia and Complex Device Nurse Practitioners. The department encourages active involvement with professional bodies, and has regular representation at council level with BSE, BHRS and BCIS. We are a practical assessment centre for BSE and participate in the STP OSFA assessments for the National School of Healthcare Science. Professional development is encouraged at all levels. We are a National School of Healthcare Science accredited training centre. Professional registration is preferred i.e., RCCP or AHCS We would consider flexible working patterns. Oxford University Hospitals NHS Foundation Trustis one of the largest NHS teaching trusts in the country. It provides a wide range of general and specialist clinical services and is a base for medical education, training, and research. Find out more here www.ouh.nhs.uk The Trust comprises four hospitals - the John Radcliffe Hospital, Churchill Hospital and Nuffield Orthopaedic Centre in Headington and the Horton General Hospital in Banbury. Our values, standards and behaviours define the quality of clinical care we offer and the professional relationships we make with our patients, colleagues, and the wider community. We call thisDelivering Compassionate Excellenceand its focus is on our values of compassion, respect, learning, delivery, improvement and excellence. These values put patients at the heart of what we do and underpin the quality healthcare we would like for ourselves or a member of our family. Watch how we set out to deliver compassionate excellence via the OUH YouTube channel . • To support the Head of Cardiac Physiology in all operational/managerial matters as required e.g. effective use of resources, management of cardiac physiology personnel. In collaboration with the Band 7 group create, support and develop a dynamic cardiac physiology team with a unified vision for future planning and development of the department. To implement and support quality initiatives within Cardiac Medicine, in collaboration with the Band 7 group, by utilising effective use and monitoring of standards, auditing and evaluation of the echocardiography service in order to meet the needs of patients within this speciality. To work with the Band 7 group to ensure procedures are in place to facilitate the achievement of Trust targets for cardiac medicine such as achieving diagnostic test waiting times and implementation of clinical governance frameworks. In collaboration with the Head of Cardiac Physiology, lead the development and evaluation of relevant protocols, guidelines and procedures based on current evidence/research and facilitate /support other staff to do the same. To monitor activity within the clinical area whilst ensuring that staffing levels and skill mix meet clinical requirements. To promote awareness and understanding in others of efficient resource utilisation through education and example. In collaboration with the Band 7 group to ensure that all new staff has an appropriate induction and orientation and assigned mentor. To improve and develop Cardiac Physiologist roles Planned interview date: to be confirmed • STP/ BSc Clinical Physiology or equivalent, • Relevant experience performing at Band 6 level, • Demonstrates ability to support junior and senior members of staff, • Evidence of ongoing professional development, • Evidence of leadership development, • Recognised teaching /assessing qualification, • Evidence of Masters level study, • Demonstrable experience in a broad range of cardiac physiological procedures, such as ECG, Exercise Tolerance Testing supervision, Echocardiography, continuous ambulatory monitoring preparation and analysis, haemodynamic monitoring/recording during cardiac angiography & complex coronary intervention, implant and follow up of brady/tachy devices and Electrophysiological procedures., • Experience in co-ordinating or managing a team, • Professional attitude, takes pride in work, • Patient centred approach, compassionate, • Role model, open and honest in communication and delivers over and above what is expected, • Respectful to colleagues and patients, respects diversity. Works well within a team, • Committed to professional development of self and team, • Ability to learn from successes and setbacks, • Open to change, • Effective communication skills (verbal and written, • Demonstrates adaptability /flexibility and a positive approach to challenges, • Able to cope under pressure, • Decision making and problem solving skills, • Professional appearance and compliance with policies, • Ambitious and enthusiastic, • Evidence of professional development Sexual Safety Charter : In 2023NHS England launched its first sexual safety charter, and our Trust proudly signed it. We pledge zero tolerance for inappropriate sexual behaviour and commit tothe ten core principles Oxford University Hospitalspromotes a safe, respectful hiring environment. Vacancy Closures: Please note, this vacancy may close early if a high volume of applications are received. Visa and Immigration: Oxford University Hospitals NHS Foundation Trust is able to offer Certificates of Sponsorship for all eligible roles for a Skilled Worker Visa without exception, provided the role meets the minimum salary and skill level criteria set by the Home Office (UKVI). All eligible candidates will be considered with equal consideration at all stages of the application and recruitment process. Skilled worker: Health and Care Visa | NHS Employers / Work in the UK - GOV.UK COVID-19: The COVID-19 vaccination remains the best way to protect yourself, your family, your colleagues and of course our patients from the virus when working in our healthcare settings. Whilst COVID-19 vaccination is not a condition of employment, we do encourage our staff to get vaccinated. If you are unvaccinated there is helpful advice and information at Oxfordshire County Council Website where you can also find out more about how to access vaccination. Probation Period: This post is subject to a 6 month probationary period. If you currently hold a contract of employment with the Oxford University Hospitals, this will not apply. This statement does not apply to Medical staff or Executive Appointments. Referencing: When providing employment reference details please provide correct work related email addresses so references can be sought promptly when we are looking to progress your application. Your first referee will need to be your line manager, supervisor or clinical lead from your current or most recent post or place of study. Please note that if you have previously worked for the Trust we will require a reference from your last Manager, this information is essential if your offer of employment is to be confirmed. To note: Applicants must write their own applications. If AI tools are used, the application may be rejected as this document is crucial for assessment. This does not prevent you from seeking support via AI with applications for the purposes of any disability and/or long-term health conditions. When using AI to help write your application, it is important to personalise it, especially your supporting statement. While AI can simplify the process, it will not fully understand the job's requirements and/or be able to showcase your skills, knowledge, and experience. Write your statement to show why you are interested in the role and how you would be a valued member of the team/OUH employee. No unsolicited recruitment agency telephone calls or emails. This post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service. Please note that this job advertisement will close automatically once the application limit is reached, regardless of whether this occurs before the advertised closing date. andBand 2 Healthcare Support Workerrecruitment iscentralised, meaning when you apply you will be considered fora number of rolesacross the Trust. If you have any questions please email: . Domestic / catering / porteringservices at theJohn Radcliffe Hospitalare provided byMitie. Domestic / catering / portering / maintenance engineerservices at theChurchill HospitalandNuffield Orthopaedic Centreare provided byG4S. Maintenance engineer services at the John Radcliffe Hospital are provided by Equans. All meetings and interviews will be scheduled on Microsoft Teams from a verified OUH email account. If you have any doubts about any correspondence around recruitment, please contact us To use ReachDeck to listen to or translate this site you must You can view our departments and services alphabetically. Some areas also have dedicated microsites, which are featured in the linked images below. "Oxford University" is a registered trade mark of the University of Oxford, and is used with the University's permission. #J-18808-Ljbffr

At the Ellison Institute of Technology (EIT), we’re on a mission to translate scientific discovery into real world impact. We bring together visionaryscientists, technologists, engineers, researchers, educators and innovatorsto tackle humanity’s greatest challenges in four transformative areas: • Health, Medical Science & Generative Biology, • Food Security & Sustainable Agriculture, • Climate Change & Managing CO₂, • Artificial Intelligence & Robotics This is ambitious work - work that demands curiosity, courage, and a relentless drive to make a difference. At EIT, you’ll join a community built on excellence, innovation, tenacity, trust, and collaboration, where bold ideas become real-world breakthroughs. Together, we push boundaries, embrace complexity, and create solutions to scale ideas from lab to society. Explore more at www.eit.org. We are looking for a Laboratory Technician with demonstrable experience to assist in the smooth and efficient operation of our laboratories by providing essential logistical, maintenance and support functions. This role will support our laboratory services, supporting cutting‑edge research. This is a fantastic opportunity for someone interested in laboratory operations to further their hands‑on experience in a dynamic, fast‑paced, collaborative research environment. This role will be responsible for maintaining the laboratories cleanliness, organisation and overall operational efficiency. It will involve supporting laboratory staff with basic technical tasks, inventory management and ensuring that the laboratory environment meets the required standards for safe and effective research. The ideal candidate will be detail‑orientated, able to multitask and demonstrate excellent communication skills, with a strong focus on maintaining laboratory supplies, equipment and workflow. Hours of work will generally be Monday to Friday, core hours 08:30 – 17:30 and will be office/site based. However, due to the nature of the role and organisation there may be times where flexibility is required during the evening and occasionally weekends. • General laboratory maintenance with guidance from Scientific Operations Manager and existing technicians., • Keep the laboratory clean and organised, including regularly cleaning common spaces and ensuring waste streams are appropriately managed., • Ensure that all equipment is properly received, logged, stored, calibrated, and maintained. Assist with equipment setup and basic troubleshooting where requested., • Act as point of contact for maintenance and servicing from external stakeholders, ensuring laboratory code of conduct is maintained throughout visits., • Disinfect and sterilise laboratory tools, consumables, and areas according to established protocols or where requested., • Ensure that laboratory safety standards are adhered to, including proper handling and disposal of waste materials., • Assist in managing inventory of reagents, consumables, and laboratory supplies., • Keep accurate records of inventory levels, assist with ordering new stock, and ensure that supplies are replenished in a timely manner., • Work alongside finance business partners and procurement to ensure that logistics and deliveries are maintained, and adequate equipment/instruments have been specified and procured., • Ensure that all reagents and materials are correctly labelled, stored, and easily accessible for workflows., • Assist with the transport and preparation of biological samples, ensuring that proper documentation and labelling procedures are followed., • Handle and deliver consumables or samples to designated researchers or technical teams., • Assist with maintaining a safe and compliant laboratory environment by adhering to health and safety guidelines., • Assist in monitoring laboratory conditions, including temperature‑sensitive storage for reagents or biological samples., • Help to ensure that laboratory personnel are following all safety protocols and that safety equipment (e.g., personal protective equipment, eyewash stations) is properly maintained and accessible., • BSc qualification in a related field., • Experience in laboratory maintenance and familiarity with basic laboratory techniques and safety protocols., • Strong attention to detail and a focus on organisation and cleanliness., • Ability to follow instructions and maintain accurate records., • Good communication skills and the ability to work effectively within a team., • Ability to manage time efficiently and handle multiple tasks., • Basic understanding of laboratory safety practices and handling of biological materials., • Comfortable with lifting and moving supplies and equipment, as well as standing for extended periods., • Experience with AI & Robotics or Device Engineering is not essential, but highly desirable., • Competitive salary + travel allowance + bonus, • Enhanced holiday. Our annual leave allowance is 25 days plus 8 bank holidays and an additional 3 days between Christmas and New Year. You will also have the opportunity to purchase an additional 5 days annual leave in January and July., • Pension - Employer contribution 7.5%, minimum employee contribution 5%, • Life Assurance., • Income Protection, • Private Medical Insurance as standard for you, your partner and any dependents. Including hospital Cash Plan, • Employee discounts, • Electric car scheme, • Nursery Salary Sacrifice scheme, • Cycle to Work Scheme, • Family Planning, • Neurodiversity support including advise and assessments, • Coaching & Therapy services, • You must have the right to work permanently in the UK with a willingness to travel as necessary. We do not offer sponsorship for this role., • You will live in, or within easy commuting distance of, Oxford (or be willing to relocate) and can commit to being site based during the week with occasional weekend working., • We are looking for the Laboratory Technician to start as soon as possible. #J-18808-Ljbffr

We are an AI healthcare company dedicated to revolutionizing early interception and treatment of lung disease, starting with the deadliest: lung cancer. We support clinicians in making life‑saving treatment decisions on behalf of their patients. To do this, we have developed the world’s first FDA‑cleared product for AI‑powered diagnostic support for lung cancer, and we are working to expand our platform to drive optimal decisions across the patient journey. You will drive the future of Optellum’s pioneering platform, the first FDA cleared solution for AI‑powered lung cancer diagnosis, to ensure it is used to enable optimal care for every patient in every clinic and will lead expanding Optellum’s platform beyond early diagnosis into precision oncology AI decision support across the care pathway. You will help drive the product vision, as well as own the high‑level roadmap, scope and positioning, working directly with Chief Product Officer. You will also lead the launch of products, development of collateral, and delivery of training. You will work closely with teams across the company, as well as with external stakeholders, including reference sites, customers, Key Opinion Leader (KOL) advisors, and industry partners. • Own the product vision and high‑level roadmap for Optellum's platform across diagnosis and precision therapy, working directly with the Chief Product Officer., • Identify and prioritize unmet needs across the lung cancer patient journey, from early detection and diagnosis through to therapy guidance., • Improve in‑market products using customer feedback, market insights and key collaborations., • Design the end‑to‑end clinical workflow for each product or combination of products., • Select and coordinate work with light‑house clinical reference sites and KOLs, guide market testing or piloting of prioritized concepts, and help scale what works., • Partner with sales and marketing on customer conversations, new product launches, positioning, and go‑to‑market execution., • Support regulatory submission, working with RA, the CPO and the CTO to draft and submit new products to obtain clearances in the US, Europe/UK and the rest of the world., • Partner with Customer Success to ensure key accounts succeed and support the Product Owner in prioritizing the feature backlog, release planning and maintenance., • Create alignment across Product, Engineering, Clinical, Marketing, Market Access and leadership on priorities, progress, risks, and product decisions., • Analyze and prioritize expansion into other disease states based on unmet needs and market opportunity, in line with commercial and partnering opportunities., • Lead and prioritize geographic market expansion, selecting which markets to enter and how, and leading early accounts to routine use of our products. We are looking for an entrepreneurial innovator with a passion for healthcare, complemented by strong communication and technical skills, strategic mindset and a drive to deliver pioneering clinical products. You learn fast, you are pragmatic, you thrive in fast‑paced environments where things need to be built and where you need to switch between many different topics. • 5+ year product-related experience , preferably in a Product Management role including time spent in healthtech or another regulated, safety‑critical industry., • User empathy and genuine interest in clinician workflows, and the willingness to travel and spend real time onsite with clients., • Excellent UX judgment, with a demonstrated ability to turn technical constraints into simple, intuitive workflows for non‑technical users., • Entrepreneurial drive and passion for great products: you have a strong entrepreneurial spirit, can strongly empathize with your users, and understand their clinical and commercial needs, • Goal execution oriented: willingness to learn as well as ability to handle multiple responsibilities and excellent project management skills to complete work on time and to the required quality., • Healthcare experience: several years of experience working in healthcare domains , with proven ability to understand and impact complex drivers of adoption of novel clinical products, • Adaptability & strategic mindset : you are a quick learner, feel comfortable navigating uncharted and ambiguous landscapes, break complex problems down into simple ways, and prioritize solutions, • Team player : you have demonstrated excellence in working collaboratively and effectively with a diverse range of internal and external stakeholders, in clinical, technical and commercial roles, • Excellent written and spoken communication skills : you are effective in tailoring a message to the appropriate audience with an ability to craft clear, compelling presentations and written material, • Location and travel : willingness and ability to travel globally to tradeshows and customer meetings (25% on average, with more frequent travel in certain periods). Optellum supports remote work. Your location should allow presence in Oxford, UK 1-2 days per week when needed, • Right to work in the UK (No Visa sponsorship available), • Medical imaging AI: experience with imaging‑based AI products, and familiarity with concepts such as neural networks, • Hands‑on experience with integration to EMR or other key IT hospital systems., • Regulated product experience: hands‑on experience developing medical device software in a regulated environment, including contributing to FDA clearance and/or CE marking, • Early‑stage or pre‑market products: you have worked on a product before it had regulatory clearance or a defined market, • Early‑stage startup or fast‑growing SME experience, ideally in software, a strong plus, • Understanding of clinical workflows (pulmonology / respiratory, surgery and radiology) and healthcare systems in the US, UK, EU and other geographies., • Strong familiarity with medical imaging and/or healthcare IT domains (EMR, PACS), • Understanding of lung cancer (other lung diseases and other cancers a plus), • International experience (work or study abroad) esp in North America, Europe and APAC, • Experience working within regulated environments (e.g. ISO 13485), • Work that is both challenging and rewarding and has a real positive impact on people's lives, • Fast growth, ownership, and high impact in a growing startup, • A culture of continuous learning and professional development to help you develop your skills, • Flexible working hours and location – must be able to attend the Oxford Office when required by the ongoing projects, • Competitive salary, reviewed annually, • A discretionary annual bonus based on company and individual performance, • 25 days' annual leave per year plus public holidays, • Auto‑enrolment pension scheme with employer contributions, • Private health care through AXA Health, plus a Medicash cash plan for routine dental, optical, and physiotherapy costs, • Group life assurance at four times your annual salary, and group income protection paying up to 75% of salary, • A confidential Employee Assistance Programme, available 24/7 to you and the adults in your household, plus a health and wellbeing app, • Cycle to Work scheme, • Great location in Oxford: just 10 min walk to train station, 1h to central London #J-18808-Ljbffr

Oxford Ionics, now part of IonQ, is pioneering the next generation of quantum computing. Using our world-leading trapped-ion technology, we’re building the most powerful, accurate and reliable quantum systems to tackle problems that today’s supercomputers cannot solve. Joining Oxford Ionics means becoming part of a global IonQ team that is transforming the future of quantum technology - faster, at scale, and with real world impact. IonQ, Inc. [NYSE: IONQ] is the world’s leading quantum company delivering solutions to solve the world’s most complex problems. IonQ’s newest generation quantum computers, IonQ Tempo and IonQ Forte Enterprise, are the latest in cutting-edge systems that have been helping customers and partners such as Amazon Web Services, AstraZeneca, and NVIDIA achieve 20x performance results. The company achieved 99.99% two-qubit gate fidelity, setting a world record in quantum computing performance in 2025. The company is accelerating its technology roadmap and intends to deliver the world’s most powerful quantum computers with 2 million qubits by 2030 to accelerate innovation in drug discovery, materials science, financial modeling, logistics, cybersecurity, and defense. IonQ’s advancements in quantum networking position the company as a leader in building the quantum internet. What to expect: We're looking for an enthusiastic and highly technical Software Engineer for our Non-Realtime Controllers team who will thrive in our dynamic cross-disciplinary environment. In this role, you will be responsible forworking closely with our software engineers, our systems team, and our quantum scientists to build and operate the software that controls the hardware surrounding our quantum computers, contributing to the team’s mission of enabling our systems team to operate the physical quantum computers and our science teams to experiment building towards fault tolerant computation. Previous exposure to quantum systems is not required. You’ll play an important part in shaping the non-realtime controllers, the system operations and services that support our work in building the world’s most advanced quantum systems. What you'll be responsible for: In this position, you will work hands-on with hardware control end to end, from the device protocol up to a service running reliably across our fleet, supporting the effective delivery of non-realtime controllers that ensure that the critical supporting hardware of a quantum computer is observable, controllable and reliable (from cryogenic compressors to lasers, wavemeters, and various sensors). You’ll have the opportunity to own areas of the hardware control surface end to end, from the device protocol up to a service running reliably across our fleet, contributing directly to the success of building utility-scale quantum computers. Key responsibilities include: • Own a group of device controllers end to end, covering API design, implementation, rollout and ongoing operational health, • Make services robust against the ways real instruments fail and strengthen observability, health checking and alerting, • Bring devices onto our current framework, and roll the result out across the fleet without disrupting running experiments, • Work closely with the software. systems and science teams who depend on these services, and to ensure our work integrates seamlessly with the wider software architecture What you’ll need: To be successful, you will need strong programming skills in a systems programming language and hands-on experience interfacing with hardware, and a track record of making software behave well against unreliable external dependencies. We’re looking for someone who can quickly iterate on low-level code in a collaborative, cross-disciplinary, environment and contribute effectively within a fast moving, highly technical team. You’d be a great fit with: • Strong programming skills in one or more systems programming languages and the appetite to work in a Rust codebase, • Experience with some hardware instrument and communication protocols (e.g. SCPI, serial, TCP/IP, USB, or similar), • Comfortable owning the production behaviour of what you build, not just its correctness in test, • Excellent communication skills both within software and across disciplines, and an interest in helping other engineers get better at the craft without wanting to stop building yourself So why us? Be part of a team that’s shaping the future of quantum. We offer more than just a role, you’ll join a world class community of scientists, engineers and innovators working to unlock the full potential of quantum computing. We offer a range of benefits, including opportunities to further your career alongside industry leaders, a competitive salary with IonQ stock options, an annual performance bonus, generous annual leave, flexible hybrid working, private medical and dental insurance for you and your family, and much more. Join us and be part of the future of quantum computing. We’re proud to be an equal opportunity employer and welcome applicants from all backgrounds. #J-18808-Ljbffr

About IonQ: IonQ, Inc. [NYSE: IONQ] is the world’s leading quantum platform and merchant supplier - delivering integrated quantum solutions across computing, networking, sensing, and security. IonQ’s newest generation of quantum computers, the IonQ Tempo, is the latest in a line of cutting-edge systems that have been helping customers and partners including Amazon Web Services, and AstraZeneca achieve 20x performance results and accelerate innovation in drug discovery, materials science, financial modeling, logistics, cybersecurity, and defense. In 2025, the company achieved 99.99% two-qubit gate fidelity, setting a world record in quantum computing performance. Headquartered in College Park, Maryland, IonQ has operations in California, Colorado, Massachusetts, Tennessee, Washington, Italy, South Korea, Sweden, Switzerland, Canada, and the United Kingdom. Our quantum computing services are available through all major cloud providers, while we also meet the needs of networking and sensing customers across land, sea, air, and space. IonQ is making quantum platforms more accessible and impactful than ever before. Location: Oxford, England, UK Working pattern: Hybrid We are looking for a Senior Silicon Validation Engineer to join our Cryo-CMOS IC team at IonQ Oxford. You will lead the validation and characterisation of analogue and mixed-signal ASICs for our trapped-ion quantum processors, from test planning and platform development through first-silicon bring-up, debug and system integration. This is a hands-on technical role. You will shape our validation architecture, build reusable hardware and software, and provide the evidence needed to make confident silicon acceptance decisions. The work includes room-temperature silicon validation and silicon characterisation at cryogenic temperatures (around 4 kelvin), on packaged parts, chip-on-board assemblies and bare die on a cryogenic probe station. You will own validation delivery across chip and system interfaces, working closely with analogue and digital design, verification, modelling, firmware and systems engineers. You will turn requirements into measurable tests, prepare platforms before silicon arrives and resolve failures across the chip, board and software. As a Senior engineer, you will set technical standards, guide other engineers and improve coverage, repeatability and test efficiency across successive ASIC generations. • Own the silicon validation strategy, plans, acceptance criteria and readiness reviews, with traceability from block and system requirements to tests, results and unresolved risks., • Present the silicon acceptance report to the Cryo-CMOS IC Lead and programme stakeholders., • Lead first-silicon bring-up and characterisation of sample-and-hold and switch arrays, DACs, ADCs, references, amplifiers, switches, regulators, clocking and device-level test structures, across supply, temperature, operating modes and device variation, with sound calibration and measurement uncertainty., • Develop validation boards, fixtures and reusable Python automation, instrument drivers and regression suites, addressing signal integrity, grounding, power integrity and measurement access, with version-controlled tests and reproducible data analysis., • Plan and lead cryogenic measurements with specialist colleagues, including bare-die probing and the cold signal chain, and drive failures to root cause, separating silicon defects from board, firmware and test artefacts and correlating results with simulations, device models and foundry or partner data., • Influence testability before tape-out, coordinate validation with external design partners, the foundry and other IonQ sites., • Lead technical reviews, mentor engineers and document methods to improve throughput, data quality and reuse. You will bring substantial experience in analogue or mixed-signal silicon validation and characterisation, with ownership of multiple silicon bring-up programmes. A degree in electrical or electronic engineering, or equivalent practical experience, is expected. You should combine hands-on laboratory skills with sound judgement on test coverage, measurement confidence and programme risk. • Strong electronics fundamentals and experience validating precision signal chains, data converters or power-management circuits, including their digital control interfaces., • Practical expertise with oscilloscopes, precision sources and meters, signal generators, spectrum and logic analysers; confidence designing reliable low-noise, low-leakage measurements., • Strong Python programming for instrument control, automated testing and statistical analysis; disciplined use of Git or equivalent version control and maintainable test software., • Experience designing and debugging test PCBs, reviewing layouts and working with interfaces such as SPI, I2C, JTAG and custom shift-register chains, alongside embedded firmware or FPGA-based platforms., • A record of resolving complex chip, board and software interactions through structured experiments and collaboration., • Experience leading technical projects, mentoring engineers and communicating evidence, uncertainty and decisions in clear written reports. Useful additional experience includes cryogenic or other extreme-temperature testing; wafer or bare-die probing; early-stage IP or test-chip evaluation; FPGA development and C/C++ ; circuit simulation; and production test correlation. Prior quantum computing is welcome but not required. Be part of a team that’s shaping the future of quantum. We offer more than just a role, you’ll join a world class community of scientists, engineers and innovators working to unlock the full potential of quantum computing. We offer a range of benefits, including opportunities to further your career alongside industry leaders, a competitive salary with IonQ stock options, an annual performance bonus, generous annual leave, flexible hybrid working, private medical and dental insurance for you and your family, and much more. Join us and be part of the future of quantum computing. We’re proud to be an equal opportunity employer and welcome applicants from all backgrounds. Compensation will vary based on individual factors such as education, qualifications, and experience of the final candidate(s), specific office location, and calibration against relevant market data and internal team equity. Posted base salary figures are subject to change as new market data becomes available. Our benefits include comprehensive medical, dental, and vision plans, matching 401(k), unlimited PTO and paid holidays, parental/adoption leave, legal insurance, and a home technology stipend. Details of participation in these benefit plans will be provided when a candidate receives an offer of employment. At IonQ, we believe in fair treatment, access, opportunity, and advancement for all while striving to identify and eliminate barriers. We empower employees to thrive by fostering a culture of autonomy, productivity, and respect. We are dedicated to creating an environment where individuals can feel welcomed, respected, supported, and valued. We are committed to equity and justice. We welcome different voices and viewpoints and do not discriminate on the basis of race, religion, ancestry, physical and/or mental disability, medical condition, genetic information, marital status, sex, gender, gender identity, gender expression, transgender status, age, sexual orientation, military or veteran status, or any other basis protected by law. We are proud to be an Equal Employment Opportunity employer. The position you are applying for will require access to technology that is subject to U.S. export control and government contract restrictions. Employment with IonQ is contingent on either verifying "U.S. Person" (e.g., U.S. citizen, U.S. national, U.S. permanent resident, or lawfully admitted into the U.S. as a refugee or granted asylum) status for export controls and government contracts work, obtaining any necessary license, and/or confirming the availability of a license exception under U.S. export controls. Please note that in the absence of confirming you are a U.S. Person for export control and government contracts work purposes, IonQ may choose not to apply for a license or decline to use a license exception (if available) for you to access export-controlled technology that may require authorization, and similarly, you may not qualify for government contracts work that requires U.S. Persons, and IonQ may decline to proceed with your application on those bases alone. Accordingly, we will have some additional questions regarding your immigration status that will be used for export control and compliance purposes, and the answers will be reviewed by compliance personnel to ensure compliance with federal law. Due to applicable export control laws and regulations, candidates must be a U.S. citizen or national, U.S. permanent resident (i.e., current Green Card holder), or lawfully admitted into the U.S. as a refugee or granted asylum. Accordingly, we will have some additional questions regarding your immigration status that will be used for export control and compliance purposes, and the answers will be reviewed by compliance personnel to ensure compliance with federal law. #J-18808-Ljbffr

The department opening hours are between 8-6 Monday to Friday and some Saturday working. Working on the bank means you are not contracted to a set number of hours per week but instead work on an ad-hoc basis to suit the needs of the business and your availability. The intervention suite completes a range of procedures including; cardiac device implantation such as Pacemakers, CRT, ICDs and cardioversion in addition to Radiology interventional procedures. As well as scrubbing and circulating for cases, you will be involved in the patient journey from start to finish, including pre-assessment outpatient work, patient follow up and supporting wards and recovery with your expertise. You’ll also work with a range of consultants whilst developing your own skills in the cardiology environment. • Providing a specialist private cardiac service to patients requiring cardiac device implantation and cardioversion., • Being involved in the whole patient journey from pre-assessment to discharge ensuring patients individual needs are met and planned accordingly., • Acting as scrub nurse to Consultant Cardiologists and promote and maintain a caring and highly professional standard of nursing, meeting the needs of the patients undergoing Cath Lab procedures., • Working with the cardiology ward/recovery staff ensuring patients are admitted and prepared for Cath Lab procedures ensuring appropriate investigations are done and accurately recording documentation., • To be an RN with post registration experience., • Experience of working in a Cardiac Catheter lab environment., • Initiative to manage your own clinical workload within a small team. We want you to love coming to work, feeling healthy, happy and valued. That’s why we’ve developed a benefits package with you in mind. • Holiday in line with the working time directive., • Access to our pension scheme., • Discounted gym membership at £35.00 a month. Nuffield Health Oxford. Our modern hospital is based within a stone’s throw of the historic City of Oxford, a world-renowned centre of excellence for surgical and medical expertise. We are proud of the wonderful environment and team we have established, providing our patients with first class care. We operate 6 well equipped and modern operating theatres with 64 well-presented ensuite rooms. We cater for inpatient and day care, providing a broad range of surgical specialties and clinics including Paediatrics, Oncology, Interventional Cardiology & Radiology, Orthopaedics, Endoscopy, Gynaecology, Urology, Ophthalmology as well as women’s and men’s health clinics. The hospital is located with excellent transport links by road and rail, both to and from London, Thames Valley, and the Midlands. Join Nuffield Health and create the future you want, today. Nuffield Health, is the UK’s largest healthcare charity. For over 60 years, we’ve been working to make the UK fitter, healthier, happier and stronger. All for the public benefit. We do this through our family of 31 award-winning hospitals, 113 fitness and wellbeing centres, healthcare clinics and over a 100 workplace wellbeing services. As a charity, we reinvest all our income into our services, into pioneering improvements in care, and most importantly into our social impact programmes, which are designed to support people who would not normally be able to afford or access our services. Its all part of our mission to give everyone the care they need and to build a healthier nation. #J-18808-Ljbffr

Oxford Nanopore Technologies: Our goal is to bring the widest benefits to society through enabling the analysis of anything, by anyone, anywhere. The company has developed a new generation of nanopore-based sensing technology for faster, information rich, accessible and affordable molecular analysis. The first application is DNA/RNA sequencing, and the technology is in development for the analysis of other types of molecules including proteins. The technology is used to understand and characterise the biology of humans and diseases such as cancer, plants, animals, bacteria, viruses, and whole environments. With a thriving culture of ambition and strong innovation goals, Oxford Nanopore is a UK headquartered company with global operations and customers in more than 125 countries! We are looking for a highly motivated Software Automation Test Engineer to carry out the quality assurance stage of software development for our primary sequencing software. As part of our team, the Software Automation Test Engineer will conduct and design automated and manual tests, as per the defined standards and procedures, to ensure the software built by our developers is fit for purpose. You'll find yourself working in cross-functional teams with software developers and project teams to deliver test plans, test cases, automated tests and reports on functional and non-functional requirements in a fast-paced agile environment. • Testing software releases by carrying out assigned tests, • Generating and completing test cases based on requirements, • Designing tests to mitigate risk, • Writing bug reports and providing objective feedback to software development teams, • Platform testing to include: desktop, tablet and mobile across Linux, OSX and Windows, • Working towards departmental and project deadlines, • Communicating findings to technical and non-technical colleagues We'll expect you to have an undergraduate degree or equivalent experience and professional qualifications. You'll also be experienced in automated testing with proven knowledge of testing desktop and/or mobile software. • Programming language such as Python or JavaScript, • Writing automated tests in a framework such as Pytest, Jest, Robot or Behave, • Writing UI tests in a framework such as WebdriverIO, Cypress or any Selenium based framework, • A solid understanding of the software development life-cycle and testing methodologies, • Behaviour Driven Development (BDD) approach, • ReST API and/or gRPC, • Virtualisation technology such as Docker, • Linux/Unix, • JIRA and XRay Test Management for JIRA, • Testing for medical device softwar As liaising with a variety of different collaborators is a regular part of this role, we're looking for someone with excellent verbal and written communication skills and an approachable manner that encourages interaction with others. You're also someone with a good eye for detail and excellent organisational abilities that enable you to work towards and achieve tight deadlines. This role will suit someone who works well under pressure, and who wants the challenge of being part of a fast-paced high-tech organisation. You will sometimes need to work with the team at our Oxford offices therefore you must be able to commute to our HQ based in Oxford. We offer outstanding benefits to include an attractive bonus, generous pension contributions, private healthcare and an excellent starting salary. Please note that no terminology in this advert is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Every candidate will be assessed only in accordance with their merits, qualifications and abilities to perform the duties of the job. Oxford Nanopore Technologies: Our goal is to bring the widest benefits to society through enabling the analysis of anything, by anyone, anywhere. The company has developed a new generation of nanopore-based sensing technology for faster, information rich, accessible and affordable molecular analysis. The first application is DNA/RNA sequencing, and the technology is in development for the analysis of other types of molecules including proteins. The technology is used to understand and characterise the biology of humans and diseases such as cancer, plants, animals, bacteria, viruses, and whole environments. With a thriving culture of ambition and strong innovation goals, Oxford Nanopore is a UK headquartered company with global operations and customers in more than 125 countries. #J-18808-Ljbffr

About IonQ: IonQ, Inc. [NYSE: IONQ] is the world’s leading quantum platform and merchant supplier - delivering integrated quantum solutions across computing, networking, sensing, and security. IonQ’s newest generation of quantum computers, the IonQ Tempo, is the latest in a line of cutting‑edge systems that have been helping customers and partners including Amazon Web Services, and AstraZeneca achieve 20x performance results and accelerate innovation in drug discovery, materials science, financial modeling, logistics, cybersecurity, and defense. In 2025, the company achieved 99.99% two‑qubit gate fidelity, setting a world record in quantum computing performance. Headquartered in College Park, Maryland, IonQ has operations in California, Colorado, Massachusetts, Tennessee, Washington, Italy, South Korea, Sweden, Switzerland, Canada, and the United Kingdom. Our quantum computing services are available through all major cloud providers, while we also meet the needs of networking and sensing customers across land, sea, air, and space. IonQ is making quantum platforms more accessible and impactful than ever before. Location: Oxford, UK Office commitment: Hybrid Quantum is now, and it's built here. Oxford Ionics, now part of IonQ, is pioneering the next generation of quantum computing. Using our world‑leading trapped‑ion technology, we're building the most powerful, accurate and reliable quantum systems to tackle problems that today's supercomputers cannot solve. We're looking for an enthusiastic and highly technical Staff Software Engineer for our non‑realtime controllers team who will thrive in our dynamic cross‑disciplinary environment. You'd be working closely with our skilled software engineers, our systems teams who operate the physical quantum computers, and our world‑leading quantum scientists to build and operate the software that controls the hardware surrounding our quantum computers. Previous exposure to quantum systems is not required. You will take on our most demanding hardware integrations and the framework work that makes every other controller better. This is a hands‑on engineering role: you would be the most experienced engineer writing controllers, not the one directing others to write them. A working quantum computer is far more than the ion trap and its real‑time control electronics. It depends on a fleet of supporting hardware, including cryogenic compressors, vacuum pumps, power supplies, lasers, temperature controllers, wavemeters and cameras, that has to be kept observable, controllable and reliable. The timing‑critical operations such as gate waveforms and ion transport run on dedicated real‑time FPGA systems, while this team owns everything that does not need hard timing guarantees. These services run on general‑purpose Linux hardware and must be rock‑solid, because a failed compressor or an un‑noticed pressure drift takes a whole machine offline. This is a hands‑on engineering role. Your influence comes from the code you ship and review, and from the problems you take off everyone other's plate. • Take on our most demanding device integrations, and do the deep diagnosis of problems that only appear against real hardware in a live lab., • Remove whole classes of failure across the fleet, rather than instances of them., • Improve the shared framework yourself, and bring the existing controllers along with each change., • Build the tooling, simulators and test infrastructure that let the whole team move faster., • Evolve how our services are deployed and operated as the fleet grows, and make the fleet observable enough that problems are found early., • Raise the bar of everyone around you through the code you write and the reviews you give. To be successful, you will need deep systems engineering experience, a track record of shipping and operating reliable services, and the judgement to tell a problem worth solving structurally from one worth patching. We're looking for someone who wants to stay hands‑on in the code at this level rather than move away from it. • Expert systems engineering skills. Our controllers are written in Rust, so either solid Rust experience or deep proficiency in another systems language and the appetite to work in a Rust codebase, including async programming., • Experience building and operating networked services in production such as gRPC or REST, with a real grasp of error handling, observability and failure modes., • Experience of hardware and instrument protocols and interfaces such as SCPI, Modbus, serial and Ethernet., • A reputation as the person people bring the undiagnosable bug to, and the ability to prioritise work with a clear understanding of critical versus urgent items., • Excellent communication skills both within software and across disciplines. Be part of a team that’s shaping the future of quantum. We offer more than just a role, you’ll join a world class community of scientists, engineers and innovators working to unlock the full potential of quantum computing. • opportunities to further your career alongside industry leaders, • a competitive salary with IonQ stock options, • an annual performance bonus, • generous annual leave, • flexible hybrid working, • private medical and dental insurance for you and your family, • and much more Join us and be part of the future of quantum computing. We’re proud to be an equal opportunity employer and welcome applicants from all backgrounds. Compensation will vary based on individual factors such as education, qualifications, and experience of the final candidate(s), specific office location, and calibration against relevant market data and internal team equity. Posted base salary figures are subject to change as new market data becomes available. Our benefits include comprehensive medical, dental, and vision plans, matching 401(k), unlimited PTO and paid holidays, parental/adoption leave, legal insurance, and a home technology stipend. Details of participation in these benefit plans will be provided when a candidate receives an offer of employment. At IonQ, we believe in fair treatment, access, opportunity, and advancement for all while striving to identify and eliminate barriers. We empower employees to thrive by fostering a culture of autonomy, productivity, and respect. We are dedicated to creating an environment where individuals can feel welcomed, respected, supported, and valued. We are committed to equity and justice. We welcome different voices and viewpoints and do not discriminate on the basis of race, religion, ancestry, physical and/or mental disability, medical condition, genetic information, marital status, sex, gender, gender identity, gender expression, transgender status, age, sexual orientation, military or veteran status, or any other basis protected by law. We are proud to be an Equal Employment Opportunity employer. The position you are applying for will require access to technology that is subject to U.S. export control and government contract restrictions. Employment with IonQ is contingent on either verifying “U.S. Person” (e.g., U.S. citizen, U.S. national, U.S. permanent resident, or lawfully admitted into the U.S. as a refugee or granted asylum) status for export controls and government contracts work, obtaining any necessary license, and/or confirming the availability of a license exception under U.S. export controls. Please note that in the absence of confirming you are a U.S. Person for export control and government contracts work purposes, IonQ may choose not to apply for a license or decline to use a license exception (if available) for you to access export‑controlled technology that may require authorization, and similarly, you may not qualify for government contracts work that requires U.S. Persons, and IonQ may decline to proceed with your application on those bases alone. Accordingly, we will have some additional questions regarding your immigration status that will be used for export control and compliance purposes, and the answers will be reviewed by compliance personnel to ensure compliance with federal law. Due to applicable export control laws and regulations, candidates must be a U.S. citizen or national, U.S. permanent resident (i.e., current Green Card holder), or lawfully admitted into the U.S. as a refugee or granted asylum. Accordingly, we will have some additional questions regarding your immigration status that will be used for export control and compliance purposes, and the answers will be reviewed by compliance personnel to ensure compliance with federal law. #J-18808-Ljbffr

Do you want to contribute to a safer market while gaining an authentic international experience as a consultant? Obelis is currently looking for a RA Expert Consultant specialized in food supplements! As a Food Supplements Expert Consultant, you will play a key role in supporting the Regulatory Affairs Department (RA) by providing senior regulatory expertise, overseeing complex projects, and contributing to the team's performance, operational efficiency, and achievement of departmental KPIs. • 1.Lead complex regulatory projects and provide expert regulatory guidance with a focus on food supplements compliance., • 2. Review and validate complex documentation and authority interactions., • 3. Drive technical excellence and departmental expertise., • 4. Act as a trusted advisor for strategic clients., • 5. Coach colleagues and support managers in coordination activities., • 6. Participate in Obelis events (in and outside UK), • 7. Support safe market access and work in an international consulting environment. The successful candidate will support clients on regulatory matters across the UK, EU, and US, with a primary focus on food supplements and is expected to become the designated Food Supplement PRRC, supporting appropriate regulatory oversight and accountability for food supplement compliance activities., • 8. Deliver professional, responsive, and high-quality service to external and internal clients., • 9. Act as, or work towards becoming, the designated Food Supplement PRRC, ensuring appropriate oversight of food supplement regulatory compliance activities in line with internal procedures and applicable requirements., • 10. Provide regulatory support covering UK, EU, and US product requirements, with particular emphasis on food supplements and related product categories., • 11. Perform borderline assessments to support appropriate product classification, including food supplement versus medicine, medical device, cosmetic, or other regulated product categories., • 12. Assess product composition, ingredients, claims (e.g. nutrition and health claims, including permitted claims, on-hold botanical claims, disease-risk reduction claims, and the avoidance of prohibited medicinal claims), labelling, and supporting documentation for regulatory compliance., • Applicants must hold a valid UK work permit., • Bachelor's/Master's degree in Food Science, Nutrition, Pharmacy, Chemistry, Toxicology, Biology or a related scientific discipline., • 3+ years of relevant experience in the food supplement consultancy sector., • Fluency in English (written and oral). Knowledge of additional languages is a plus., • Strong knowledge of regulatory applications and documentation review, • Solid understanding of regulatory environments and their impact on clients., • Analytical mindset with the ability to translate issues into practical improvements., • Ability to work cross-functionally across teams and stakeholders. At Obelis, we believe in continuous learning and professional growth. In this role, you will further develop your expertise in: • Regulatory strategy and expert advisory, • Project and stakeholder management, • Client advisory and relationship management, • Regulatory risk assessment and decision-making, • Location: Oxford, • Full-time position Obelis s.a is a quality-driven, service-oriented company, with over 30 years of experience in EU Regulations. Providing consultancies on medical devices, cosmetics, and other consumer goods, we believe in making manufacturers better through compliance and making safe products available on the market. #J-18808-Ljbffr

At the Ellison Institute of Technology (EIT), we’re on a mission to translate scientific discovery into real world impact. We bring together visionaryscientists, technologists, engineers, researchers, educators and innovators to tackle humanity’s greatest challenges in four transformative areas: • Health, Medical Science & Generative Biology, • Food Security & Sustainable Agriculture, • Climate Change & Managing CO₂, • Artificial Intelligence & Robotics This is ambitious work - work that demands curiosity, courage, and a relentless drive to make a difference. At EIT, you’ll join a community built on excellence, innovation, tenacity, trust, and collaboration, where bold ideas become real-world breakthroughs. Together, we push boundaries, embrace complexity, and create solutions to scale ideas from lab to society. Explore more at eit.org Within this ecosystem, the Pathogen Mission exemplifies EIT’s commitment to transformative science. It aims to revolutionise the diagnosis and treatment of infectious diseases by leveraging whole genome sequencing (WGS)-based metagenomic and pathogen‑specific analytical tools. This remit includes the development of a decentralised, sample‑to‑answer sequencing diagnostic platform for infectious diseases, enabling rapid and accurate analysis of patient samples without prior assumptions. Supported by Oracle Inc.’s cloud‑computing scale and security infrastructure, the Pathogen Mission is progressing towards certified diagnostic products for deployment in laboratories, hospitals, and public health organisations worldwide. We are seeking an experienced and innovative Senior Electronics R&D Engineer to develop advanced electronic interfaces, instrumentation, and measurement systems for next‑generation nanopore sequencing technologies. This is a hands‑on role within an ambitious early‑stage development programme, taking technologies from proof of concept through to integrated, multi‑channel sensing systems. Working closely with a Senior MEMS Development Engineer, you will design, build, and test experimental electronics, develop custom instrumentation, and optimise prototype devices through iterative development. Key areas of focus include precision analogue measurement, low‑noise circuit design, multi‑channel data acquisition, electronic control systems, and system integration. You will translate emerging concepts into working prototypes, identify technical limitations, and drive continuous improvement based on experimental data. The role also involves collaborating with external suppliers and technical partners, defining requirements, overseeing outsourced development, and evaluating resulting components and systems. As the programme grows, you will help establish the electrical engineering capabilities, testing infrastructure, and technical foundations needed to support a multidisciplinary development team. • Take technical ownership of the electrical engineering development of advanced electronic interfaces and measurement systems, from early concepts through to functional prototypes and integrated devices., • Design, build and commission custom electronic test equipment and experimental platforms to characterise electrical performance, reliability and repeatability., • Develop prototype electronic circuits and sensing architectures, including multi‑channel analogue measurement systems, signal conditioning and data‑acquisition electronics., • Work closely with the Senior MEMS Development Engineer to co‑develop and evaluate prototype devices, using experimental findings to guide iterative improvements in device and instrumentation design., • Design and implement sensitive, low‑noise measurement systems capable of characterising electrical currents in the picoampere range., • Develop automated testing and data‑acquisition methods to assess electrical and sensing performance, including software for instrument control and data analysis., • Investigate electrical noise, leakage currents, signal integrity, parasitic effects and cross‑talk in multi‑channel sensing systems., • Develop and evaluate approaches to electrical grounding, shielding and electrostatic discharge (ESD) protection for sensitive electronic and electrochemical systems., • Collaborate with mechanical, MEMS and other engineering disciplines to develop experimental fixtures, prototype assemblies and integrated test platforms., • Design increasingly sophisticated electronic test platforms as the project progresses, supporting the transition from initial feasibility studies to integrated nanopore sensing systems., • Define technical requirements and specifications for external engineering suppliers, including the design and fabrication of custom electronics, components and specialist test equipment., • Coordinate technical activities with external suppliers and collaborators, reviewing designs, monitoring progress and evaluating deliverables against agreed performance requirements., • Plan and execute structured experiments, analyse performance data and translate findings into engineering requirements and design improvements., • Contribute to component selection, prototype fabrication, supplier engagement and assessments of manufacturability, scalability and cost., • Maintain clear technical documentation, design records and experimental results, contributing to intellectual property development and technical reviews while ensuring appropriate confidentiality., • Provide technical guidance and mentoring as the engineering team expands, helping establish robust engineering practices and development processes. We welcome applicants from industry, applied research and academia who can demonstrate strong technical expertise and practical engineering capability. • Degree in Electrical or Electronic Engineering, Physics or a related discipline, or equivalent relevant experience., • Significant experience in electronic engineering research and development, ideally involving novel instrumentation, sensor systems or precision measurement technologies., • Strong understanding of analogue and mixed‑signal electronics, including low‑noise circuit design, signal conditioning and measurement techniques., • Proven experience designing, building and debugging electronic hardware, including custom circuits, printed circuit boards and laboratory test systems., • Practical experience developing experimental instrumentation using laboratory equipment such as oscilloscopes, source‑measure units, precision current measurement systems and data‑acquisition hardware., • Experience developing or integrating electronic control, switching or multi‑channel measurement systems., • Ability to develop automated test methods, including scripting or programming for instrument control, data acquisition and analysis., • Experience planning and executing structured experimental programmes to characterise complex electronic systems and resolve technical challenges., • Strong understanding of electrical signal integrity, grounding, shielding and methods for minimising noise and interference., • Ability to work independently, establish technical direction and deliver working prototypes in an early‑stage R&D environment., • Experience collaborating with multidisciplinary teams and translating requirements between electronics, mechanical engineering and device fabrication., • Ability to develop clear technical specifications and work effectively with external engineering suppliers, development partners or specialist fabricators., • Experience with picoampere or similarly sensitive current measurements, including transimpedance amplifiers, leakage‑current management and low‑noise analogue front‑end design., • Knowledge of electrochemical sensing, biosensors, nanopore technologies or other low‑current sensor systems., • Experience with semiconductor devices, MEMS interfaces, microelectronic packaging or electronic sensor integration., • Familiarity with ASIC interfaces, FPGA‑based control, electronic multiplexing or multi‑channel sensor‑readout architectures., • Experience developing test equipment for evaluating the electrical performance and reliability of prototype devices., • Knowledge of ESD protection strategies for sensitive electronic devices or electrochemical sensors., • Experience with Python, LabVIEW or similar tools for automated test equipment, instrument control and data analysis., • Familiarity with precision PCB design techniques, guarding, shielding and control of parasitic capacitance., • Experience integrating prototype electronics with microfabricated devices, fluidic systems or other multidisciplinary hardware., • Experience working with external engineering companies or specialist suppliers to develop, fabricate and qualify custom components or instrumentation., • Understanding of design for manufacture, engineering reliability and transitioning prototype systems towards scalable production., • Hands‑on and inventive: Enjoys solving technical challenges through practical engineering, experimentation and rapid prototyping., • Comfortable with early‑stage R&D: Able to work effectively where solutions are not yet established and technical requirements evolve through experimentation., • Analytical and systematic: Uses sound engineering judgement and quantitative evidence to understand complex behaviour and guide design decisions., • Collaborative: Works closely with specialists in MEMS, mechanical engineering, chemistry and electronics, as well as external technical partners, to develop integrated solutions., • Independent and proactive: Can establish experimental capabilities, identify priorities and progress technical work with limited existing infrastructure., • Technically ambitious: Motivated by challenging engineering problems and developing technologies with the potential for substantial real‑world impact., • Clear communicator: Able to explain complex technical challenges, document findings and communicate requirements effectively with colleagues, suppliers and external collaborators., • Salary: Competitive + travel allowance + bonus, • Enhanced holiday pay, • Pension, • Life Assurance, • Income Protection, • Private Medical Insurance, • Hospital Cash Plan, • Therapy Services, • Perk Box, • Electric Car Scheme, • You must have the right to work permanently in the UK with a willingness to travel as necessary. In certain cases, we can consider sponsorship, and this will be assessed on a case‑by‑case basis., • You will live in, or within easy commuting distance of, Oxford (or be willing to relocate)., • You must be eligible to work in the UK with occasional travel (1-3 trips per year). #J-18808-Ljbffr

At ONI, we are driven by a profound mission: to propel scientific discovery and combat diseases by granting everyone the ability to visualize, comprehend, and share the intricate microscopic details of life. Our revolutionary Nanoimager and Aplo Scope stand at the forefront of advancing cellular studies on a molecular level, making substantial contributions to the evolution of scientific knowledge. We are actively seeking an enthusiastic and self-motivated Senior Electronics & Systems Engineer to join our pioneering team located in Oxford. We believe in the power of relentless curiosity and the pursuit of excellence, and we invite you to join us in shaping the future of scientific exploration and healthcare breakthroughs. In this role you will be the go-to technical resource for electronics design, working closely with engineering, software and R&D product teams. Electronics design is at the core of the role, but we are looking for someone who enjoys working beyond the boundaries of the PCB - developing embedded firmware, integrating sensors and actuators, and understanding how electronics interact with optics, mechanics, software and the physical world. You will have significant technical ownership across the product lifecycle, from circuit and system design through prototyping, bring-up, verification and production. You will also develop production firmware and work further up the software stack where needed to integrate, automate and test the systems you develop. The role is ideal for an engineer who enjoys solving complex multidisciplinary problems, takes ownership of product outcomes and thrives in a collaborative, fast-paced environment. • Own electronics designs from concept through architecture, schematic design, PCB development, bring-up, verification and production., • Design robust analogue and digital electronics, including power supplies, signal conditioning, sensor interfaces, communications and control electronics., • Make appropriate component and architecture choices, balancing performance, cost, availability, manufacturability and product requirements., • Undertake PCB design and layout as an integral part of electronics development, working with external PCB designers where appropriate, and considering signal integrity, grounding, noise, EMC/ESD, thermal performance and DFM/DFT., • Work with manufacturing partners and suppliers to ensure designs are manufacturable, testable and robust through production., • Bring up new hardware and systematically debug complex problems using oscilloscopes, logic analysers, hardware debuggers and other laboratory instrumentation., • Develop and maintain production embedded firmware, typically for microcontrollers, alongside low-level firmware for hardware bring-up, control, test and diagnostics., • Develop and debug interfaces to sensors, actuators and other hardware, including analogue front ends, ADCs/DACs and common digital communication interfaces., • Work with optical and mechanical engineers on optoelectronic and physical-system interfaces, such as photodetectors, lasers and other light sources, cameras, position and temperature sensing, motors, piezos and other actuators., • Diagnose issues whose root cause may lie in electronics, firmware, sensors, optics, mechanics, cabling, software or the interactions between them., • Develop test and automation tools, including Python-based instrumentation, hardware testing and manufacturing QA., • Support verification, EMC/compliance testing, production test, calibration and transfer of designs into manufacture., • Support electronics throughout the product lifecycle, including investigation of product and manufacturing issues, root-cause analysis, component obsolescence and design changes., • Apply modern software engineering practices including source control, automated testing and CI/CD, and make effective use of AI-assisted development tools and coding agents to extend and accelerate your capabilities beyond electronics., • Strong analogue and digital circuit design fundamentals., • Schematic capture, PCB layout and development of multilayer PCBs., • Power supply design, power distribution, protection and power sequencing., • Low-noise electronics, grounding, shielding and signal integrity., • Sensor interfacing, analogue signal conditioning, amplification, filtering and data conversion., • Microcontrollers and embedded systems., • Embedded C/C++, including development of robust production firmware and low-level peripheral control, interrupts, timers, DMA and real-time behaviour., • Developing from device datasheets and MCU/SoC reference manuals rather than relying solely on high-level libraries., • Interfaces such as SPI, I²C, UART, CAN, USB and Ethernet., • Practical board bring-up and fault-finding using oscilloscopes, logic analysers, multimeters and hardware debuggers., • Design for EMC, ESD, reliability, manufacturability and test., • Taking electronics through prototype, verification, certification and production., • Git and modern software development practices, and Python or similar for test, automation and instrumentation., • Working effectively across electronics, firmware, mechanical, optical and higher-level software disciplines., • Scientific instrumentation, microscopy, imaging or other precision instruments., • Optoelectronics, including photodiodes, LEDs/lasers, optical power monitoring or camera/image-sensor interfaces., • Precision or low-noise analogue electronics., • Motion control, motors, encoders, piezo actuators or feedback/control systems., • High-speed data acquisition or communications., • Production test fixtures, calibration systems and manufacturing automation., • System-level debugging across complex multidisciplinary systems, including electronics, firmware, optics, mechanics and software., • Using coding agents or other AI-assisted development tools to build test, automation or hardware-control applications. At ONI, we understand that a fulfilling career involves more than just challenging work - it’s about enjoying a well-rounded experience. When you become a part of our team, you not only contribute to groundbreaking research but also enjoy a range of benefits designed to enhance your life both inside and outside the workplace. As an equal opportunity employer, we prioritize fairness and respect, ensuring every team member thrives regardless of their background. But that’s not all - our perks include: • Competitive Compensation: We recognize and reward your talent. Enjoy a competitive salary that reflects your expertise and contributions, ensuring your hard work is recognized., • 28 days of annual leave plus 8 bank holidays and 4 dedicated wellbeing days., • Onsite Gym Facilities: Stay active and energized with our convenient onsite gym, promoting your overall health., • Private Healthcare and Dental Coverage: Your health matters to us. Access top-notch medical and dental services, ensuring your well-being is in good hands., • Inclusive Culture: Be a valued member of our diverse, inclusive family. Your unique perspective is celebrated here, fostering a culture of mutual respect and understanding., • Cycle To Work Scheme: Embrace a sustainable commute with our cycle to work program, promoting eco-friendly travel and a healthy lifestyle., • Health Assured: Your mental health is essential. Access our comprehensive mental health support services for a balanced work-life experience., • People’s Pension: Secure your future with our pension scheme, investing in your financial well-being beyond the workplace., • Perks at Work: Enjoy exclusive discounts and deals through our perks at work program, adding value to your everyday life., • Specsavers Eyecare: Your vision matters. Benefit from our eyecare program with Specsavers, ensuring your eyes stay healthy and your vision clear. If you are driven by innovation, eager to make a significant impact in the realm of scientific and medical research, and possess the skills and passion we are looking for, we invite you to apply and be a part of our mission to improve our understanding of the details of life. #J-18808-Ljbffr

OrganOx in Oxford is seeking an experienced R&D Programme Manager to lead end-to-end New Product Development across regulatory, quality, manufacturing readiness and commercial priorities. You will drive governance, risk management and stakeholder alignment across R&D, Regulatory, Quality Assurance, Operations and Clinical teams, delivering complex medical device programmes. This on-site role offers flexibility and an opportunity to shape organ preservation technology within a world-class team. #J-18808-Ljbffr

OrganOx is seeking a Senior Digital Infrastructure & DevOps Engineer to design, build, and secure cloud infrastructure that underpins our digital products and connected device services. You will mentor engineers while supporting regulated medical software development, CI/CD, and data-platform integr

Abingdon-based medical device company seeks a Production Engineering Team Lead to drive the engineering function and expand production capability for current and new products. This role blends hands-on leadership with strategic development to deliver robust, scalable production processes aligned wit