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IT ManagerOxford / Hybrid (1 day in office per week/fortnight) Profectus Recruitment is partnering with an Oxford-based organisation to appoint an experienced IT Manager to lead its technology function. This is a strategic leadership role reporting to the CFO, responsible for shaping and delivering a multi-year IT strategy while overseeing secure, reliable and compliant day-to-day IT operations. The RoleYou will own the IT roadmap across infrastructure, security, applications, data and digital tools, ensuring technology supports both current and future organisational needs. Key responsibilities include: • Leading the development and execution of the IT strategy, • Overseeing application selection, systems architecture and technology investments, • Managing and holding accountable the Managed Service Provider and technology vendors, • Experience of cyber security principles and data governance ideally specifically with ISO 27001, ISO 27701, Cyber Essentials or Cyber Essentials Plus., • Ensuring strong governance around system adoption, integration and retirement, • Driving cybersecurity, risk management and compliance (including ISO 27001, ISO 27701, Cyber Essentials and NHS DSP Toolkit), • Overseeing infrastructure performance, resilience, patching, backups and business continuity, • Leading IT projects and supporting organisational change, • Promoting effective digital collaboration and continuous improvement This is an oversight and governance-led role rather than a heavily hands-on technical position, but strong technical credibility is essential. About YouYou will have proven experience in an IT Manager or similar role, with both operational and strategic exposure. You'll bring:, • Strong knowledge of infrastructure, networks, cloud platforms and SaaS ecosystems - Experience developing IT strategy and multi-year planning - Application and technology evaluation experience - Vendor and MSP management expertise - Budgeting and forecasting responsibility - A solid understanding of cybersecurity and data governance - The ability to communicate technical concepts clearly to non-technical stakeholders - A collaborative, organised and improvement-focused approach Benefits for the position;, • Up to 8% matched pension, • Two annual pay reviews, • Life insurance at 4x salary, • Flexible working hours This is an opportunity to play a key role in shaping technology direction within a forward-thinking organisation, balancing strategy, governance and operational oversight.

Cloud Architect – Microsoft Azure Up to £70,000 (negotiable) + exceptional benefits | Permanent | Hybrid - Newbury We are looking for a Cloud Hosting Architect to lead the design, delivery, and ongoing improvement of enterprise cloud and on-site hosting platforms. You will take ownership of architecture across Azure, ensuring critical business systems are secure, scalable, resilient, and cost-effective. This is a hands-on architecture role with genuine influence, ideal for someone who enjoys shaping strategy as well as getting involved in delivery. The role • Design and deliver scalable, secure, and sustainable hosting solutions on Azure (ideally with some AWS exposure), • Lead technical discovery sessions, workshops, and site assessments, • Produce cloud architecture roadmaps and reference frameworks, • Embed InfoSec, SecOps, and data privacy principles into all designs, • Oversee solution delivery and work closely with engineers, • Produce clear technical documentation and reusable assets to support MVPs and POCs, • Ensure compliance with ISO 27001, Cyber Essentials Plus, and internal security policies, • Stay ahead of emerging technologies across cloud, AI/ML, and information security Skills and experience • Strong hands-on experience with Azure hosting and cloud technologies, • In-depth knowledge of cloud platforms, Azure essential and AWS desirable, • Experience delivering cloud migrations or IT transformation programmes, • Good understanding of enterprise architecture principles, • Confident engaging with both technical and non-technical stakeholders, • Knowledge of ISO 27001 and/or Cyber Essentials Plus If this sounds like an ideal role for you currently a Cloud Architect, Azure Cloud Architect, Cloud Solutions Architect, Hosting Architect or Enterprise Cloud Architect please apply with an up to date version of your CV for immediate consideration.

Quality Inspector £36,000 - £42,000 + Flexi Time + Training + BenefitsMonday - Friday Days, 37 Hours Per WeekDidcot - Commutable from Abingdon, Oxford, Wantage & Colsey Are you a quality inspector with CMM knowledge looking to secure your next long term challenge and move into a senior role within the business? Do you want to join a leading group who are offering flexible working hours and first class training & development? Due to continued growth, my client is looking for a quality inspector to join the team working out of their state of the art facility near Didcot. The successful applicant will become a key problem solver within the business and will lead all CMM operations within the team. You will be working with the wider quality, production and goods in departments to ensure that all company, customer and industry standards are being met while the business continues to expand. This role will offer exposure to a variety of quality standards such as ISO9001, ISO 14001, ISO 45001 and more, you will be working with bespoke and interesting products servicing the marine, energy and defence markets. This is a great time to join the business who are one of the leading companies within their sector with 2 expanding sites in the UK! With weekends off and flexible hours available this is a great opportunity for someone looking to increase their earnings and improve their work/life balance within a long term challenge. For more information please click apply and Contact Patrick Walsh - Reference4882 - The Role:Flexible Hours*Excellent training and development. The Candidate:CMM Experience/Knowledge *Commutable to Didcot Consultant: Patrick Walsh elix Sourcing Solutions is a specialist recruiter for Engineering, IT and Science roles ranging from mid to senior level positions. Please be aware that we will only accept applications from candidates that have a valid work permit to work in the UK. By applying to this job you are confirming that you do not hold a criminal record and that you know of no legal reason why you would be ineligible for employment. Inspector|Inspection|QC|QA|CMM|Faro Arm|Quality Engineer|ISO9001|Fabrication|Inspection|Test|Team Lead|Senior|Manufacturing|Welding|Welder|Manufacturer|Engineered|Engineer|Manufacturing|Testing|Inspecting|Production|Didcot|Oxford|Oxfordshire|Abingdon|Colsey|Reading|Newbury|Swindon

IT Infrastructure Engineer – Hybrid Cloud Location: Abingdon (Hybrid: 3 days on-site, 2 remote) Start: ASAP | IR35: Outside | Clearance: SC Our client is looking for an IT Infrastructure Engineer to join their Computing Division. You will deliver secure, resilient and high-performing hybrid cloud solutions while working with architects, engineers and project teams. Key Responsibilities: • Design, implement and maintain IT infrastructure including Windows Server, Hyper-V, Active Directory and networking., • Develop hybrid solutions integrating on-premises systems with Microsoft Azure., • Use infrastructure-as-code tools such as PowerShell and Terraform and automation tools such as Ansible., • Monitor and optimise system performance, availability and resilience and manage backups and disaster recovery., • Implement security controls and ensure compliance with standards such as NIST, ISO 27001 and CAF., • Produce documentation, runbooks and training materials and provide guidance to junior team members., • Work closely with stakeholders to deliver reliable and innovative IT services. Requirements:, • Experience in IT infrastructure engineering, hybrid cloud and Azure environments., • Hands-on expertise with virtualisation, networking and Windows Server administration., • Strong knowledge of security, compliance and operational best practice., • Experience with infrastructure-as-code and automation frameworks., • SC clearance and ability to work on-site in Abingdon. Apply with an up to date version of your CV for immediate consideration.

IT Manager, COR7416 This is an excellent, newly-created opportunity for an experienced and strategically-focused IT Manager to play a key role in the shaping, supporting and developing of the IT roadmap for a highly successful, not for profit organisation. Whilst the position is offered on a predominantly remote basis, the IT Manager will need to be willing and able to travel to the Oxford office as and when required, but not normally more than once a week. The Role In a highly-visible role as part of the Senior Leadership Team, the IT Manager will lead on the creation, maintenance and execution of the organisation's IT strategy and roadmap, and will be heavily involved in application selection and implementation. They will ensure that the IT infrastructure remains secure, efficient and fit for purpose, and will derive the best possible service and value from a long-standing MSP relationship that provides the day-to day IT support for approximately 70 staff (a mixture of onsite and remote) via a . In addition, the IT Manager will help the organisation to maintain it's security stance and compliance with key standards such as as ISO 27001 and Cyber Essentials Benefits: • 25 days holiday, plus an extra 3 for Christmas, • 5% Pension contribution, • Life Assurance, • Flexible hours, • A breadth of experience to be able to lead the development and delivery of the organisation's IT roadmap, • Experience of vendor management and managing third party suppliers, • Experience of application evaluation, selection and implementation, • A good awareness of IT Security/Cyber Security - Cyber Essentials and ISO 27001 experience preferred, • A broad understanding of Microsoft technical environments, including Microsoft 365 If you are an experienced IT Manager, keen to support an important organisation with the growth and development of their critical IT infrastructure, then apply now for immediate consideration! IT Manager Corriculo Ltd acts as an employment agency and an employment business. #GB #ChannelB

I'm working with an Oxford-basedcharity with an international reputation that is looking for an ITManager to take full ownership of their technology landscape and lead them through an exciting period of modernisation. This is a newly created, strategically focused role ideal for someone ready to step beyond day-to-day support and shape a long-term IT roadmap, elevate governance, and build a secure, future-ready infrastructure. The role is hybridwith 1 day a week in the Oxford office (flexible). About the Charity:This health and social-care charity is dedicated to turning people's real care experiences into meaningful improvements for patients, service users, and staff across the UK, with plans to expand internationally. Your work will directly support thousands of patients and families every year, offering a genuine opportunity to make a measurable positive impact. The Role:The charity currently partners with an external MSP for day-to-day support, and they now need a strong internal IT leader to take charge of all strategic decisions. Reporting directly to the CFO, you'll shape technology strategy and long-term planning, oversee hardware and software choices, lead modernisation projects, strengthen security, compliance, and risk management, and manage MSP performance and key vendor relationships. While you'll occasionally assist colleagues with hands-on issues, your primary focus will be leadership, planning, and continuous improvement. Key Opportunities:You'll have the autonomy to reshape systems, strengthen infrastructure, and lead technical and cultural change. You will: Modernise and redesign the tech landscape Strengthen security & compliance (ISO 27001, ISO 27701, Cyber Essentials/Plus) Partner with the Governance Manager on data governance Ensure staff feel confident and supported with technology What You'll Ideally Bring: Proven IT Manager experience Strong strategic thinking Deep Microsoft expertise Solid networking & hardware knowledge Clear understanding of data governance Excellent communication skills** Collaborative, people-focused leadership style In return, they offer hybridworking (1 day in Oxford, flexible), £57,000-£61,000 salary, up to 8% matched pension, life insurance at four times salary, flexible working around core hours, twoannualpayreviews, and full support for training and professional development (alongside other great benefits). If you're an experienced IT leader seeking real influence, autonomy, and meaningful impact, this is an excellent opportunity. Pleaseapply or contactMatthewMacAlpine at Cathcart Technology. Cathcart Technology is acting as an Employment Agency in relation to this vacancy.

Overview Pictura Bio is a well-funded University of Oxford spin-out developing a novel diagnostic platform for rapid pathogen detection. Our technology combines fluorescence microscopy with automated image analysis and machine learning to identify pathogens in seconds. The platform is being translated into clinical diagnostic products, initially focused on respiratory infections, with broader applications across infectious disease. Role Purpose The Clinical Validation Lead will be responsible for designing, executing, and overseeing clinical and analytical validation of Pictura Bio’s diagnostic assays. You will lead validation strategy from late-stage development through clinical evaluation, ensuring studies are scientifically robust, regulator-ready, and aligned with the intended clinical use. This role is ideal for someone with hands-on experience validating diagnostic assays in regulated environments, particularly US LDTs, but experience with FDA-cleared/approved, UK, or EU IVD pathways is also highly relevant. You will work closely with assay development, data science, regulatory, and external clinical partners. Major Accountabilities · Lead the design and execution of analytical and clinical validation studies for diagnostic assays · Define validation plans covering precision, accuracy, sensitivity/specificity, LoD, reproducibility, interference, and cross-reactivity · Ensure validation studies are aligned with intended use, clinical claims, and regulatory expectations · Oversee clinical sample selection, handling, and testing in collaboration with partner laboratories and CROs · Support validation of Laboratory Developed Tests (LDTs), particularly within the US regulatory framework · Contribute to validation supporting FDA (e.g. De Novo / 510(k)), UKCA, or CE-IVD pathways where applicable · Review and approve protocols, reports, and data summaries for internal and external use · Work with data science teams to ensure clinical performance metrics and analyses are appropriate and traceable · Interface with regulatory and quality teams to support technical files, submissions, and audits · Manage external stakeholders (clinical sites, reference labs, CROs) involved in validation activities · Clearly communicate validation strategy, results, and risks to senior leadership Ideal Background Education · PhD, MD, PharmD, or MSc in a relevant discipline (e.g. Clinical Sciences, Biomedical Sciences, Molecular Biology, Immunology, Microbiology) Experience · Demonstrated experience clinically validating diagnostic assays · Experience with assays such as immunofluorescence, molecular diagnostics, NGS / optical sequencing (e.g. Illumina), or imaging-based diagnostics · Experience developing or validating US Laboratory Developed Tests (LDTs) is highly desirable · Experience supporting FDA-cleared/approved assays (De Novo, 510(k), PMA) or UK/EU IVD pathways is advantageous · Experience working with clinical samples (e.g. respiratory samples, blood, urine, swabs) · Experience collaborating with hospital labs, reference labs, or CROs Skills · Deep understanding of diagnostic validation principles and study design · Strong knowledge of clinical performance metrics and statistical interpretation · Familiarity with regulatory and quality frameworks (e.g. CLIA, CAP, ISO 13485, ISO 15189) · Ability to translate clinical requirements into practical validation studies · Strong documentation, reporting, and review skills · Excellent communication skills, including interaction with clinicians, regulators, and executives Desirable Personal Attributes · Highly organised and detail-oriented, with a strong quality mindset · Comfortable taking ownership of complex, multi-stakeholder validation programmes · Scientifically rigorous but pragmatic in balancing timelines and regulatory expectations · Confident communicator who can explain validation decisions clearly · Comfortable working in a fast-moving, scaling diagnostics company

🚨 Band 6 Therapeutic Radiographer | Oxford Cancer Centre (Oxford) | ASAP Start | Permanent or Long-Term 🚨 We’re recruiting a Band 6 Therapeutic Radiographer to join the Oxford Cancer Centre in Oxford. This is an ASAP start role available on a permanent or long-term basis, ideal for a confident radiographer who thrives in a busy treatment environment and is passionate about delivering outstanding, patient-focused care. The Role You’ll support the delivery of a high-quality radiotherapy service across treatment and pre-treatment areas, working closely with the multidisciplinary team to ensure safe, accurate and compassionate care. You will: • Deliver highly complex radiotherapy treatments in line with IR(ME)R 2017 and relevant radiation regulations, • Safely operate and care for radiotherapy equipment, accurately interpreting and delivering treatment plans and prescriptions, • Support a varied patient caseload, including providing advice on treatment procedures and managing treatment-related side effects, • Maintain accurate, timely patient records and documentation, • Undertake daily assessment of patients attending for radiotherapy and refer to the wider oncology team when required, • Analyse and approve treatment verification imaging (including CBCT online/offline) and take appropriate action to maintain treatment accuracy, • Contribute to quality and safety through adherence to Quality Assurance and ISO Quality Management System procedures, • Support service improvement through participation in audits, development work, and (where appropriate) the clinical trials portfolio, • BSc Radiotherapy, • HCPC registration, • Previous NHS radiotherapy experience, • Strong anatomical knowledge and understanding of radiotherapy planning/dosimetry principles, • Knowledge of IR(ME)R 2017 responsibilities and commitment to CPD, • Experience with Varian/ARIA, • Planning systems: Eclipse and/or Somavision Apply now or message me directly for a confidential chat. 📍 Oxford Cancer Centre, Oxford 🚀 ASAP Start | Permanent or Long-Term 💼 Band 6 Therapeutic Radiographer #TherapeuticRadiographer #Radiotherapy #Band6 #OxfordJobs #NHSJobs #CancerCare #HCPC #Radiography #Oncology

An optical technology company based in Oxfordshire is seeking an experienced Mechanisms Engineer to join its growing R&D team. The successful candidate will apply their expertise in micro-mechanisms to design and develop precision components for the company’s novel optical platform. This is an exciting opportunity for a hands-on, creative mechanical/mechanisms engineer to play a key role in the development of a next-generation adaptive lens technology set to transform the way we see the world. About the Company This company’s expertise sits at the intersection of ophthalmics and optics. They develop novel ophthalmic solutions for use across optical systems, AR/VR/XR, and machine vision applications. Recognised as trusted experts in adaptive lens technology, they partner with leading global consumer electronics and technology companies to develop new solutions that optimise how we see the world. The company has developed a novel adaptive lens system that has the potential to transform visual performance in modern AR/VR/XR technologies. This breakthrough has generated significant interest across the consumer technology sector. As a result, the company is now entering the next phase of its R&D programme, scaling its technical capabilities and seeking talented engineers to join the team. This is an excellent opportunity to join a fast-growing technology company, contribute to cutting-edge R&D, and play a key role in the development of a new technology with global impact. Above all, it is an outstanding place to work, combining innovation, collaboration, and technical excellence. The Role This is an exciting period of investment and growth. The company is scaling its team and facilities to support ambitious R&D activities and is seeking an experienced Miro-Mechanisms Engineer specialising in the design and development of micro-mechanisms (e.g. micro bearings, threads, gears, and linkages), on a watch level component scale (or smaller). You will play a key role in the development of the company’s novel lens system, contributing from early concept through to production. Key Responsibilities The Mechanisms Engineer will: • Design and develop micro-mechanisms for precision optical applications, • Integrate micro-mechanisms into the company’s optical systems, • Be hands on, designing, building and testing prototypes to support iterating designs., • Provide expertise in materials selection, • Advise on best-practice manufacturing techniques, • Liaise with suppliers for the provision and manufacture of mechanisms Requirements Education Essential • Proven experience taking product concepts through to production, including design iteration, refinement, and design for manufacturing and assembly (DFX) considerations, • Experience designing micro-mechanisms, • Solid understanding of:, • Injection moulding, • Micro-moulding, • Metal stamping and forming, • Metal injection moulding, • Vacuum forming, • Knowledge of common joining processes, including:, • Adhesive bonding, • Ultrasonic welding, • Radio-frequency welding, • Heat staking, • A flair for rapid concept generation and ideation, • Strong knowledge of materials and their properties, particularly polymers and metals, • Proficiency in CAD (essential), ideally SolidWorks, • Knowledge of, and ability to work to, ISO 13485 (medical device compliance), including documentation, standards adherence, and design-for-risk-management Desirable • Competence in Geometric Dimensioning & Tolerancing (GD&T) and proficient in undertaking and documenting tolerance analysis., • Experience or exposure to optics or opto-mechanical engineering, including alignment considerations, optical component mounting, or light-path constraints, • Practical experience with Finite Element Analysis (FEA) and/or the ability to perform hand calculations, • Ability to translate product requirements into clear, complete engineering specifications, • Experience taking designs into pilot production and optimising them for scalable manufacture, • Knowledge of, and ability to work to, ISO 13485 (medical device compliance), including documentation, standards adherence, and design-for-risk-management

Mechanical Engineer – Micro-Mechanisms & Precision Systems An innovative optical technology company based in Oxfordshire is seeking a Mechanical Engineer specialising in the design and development of micro-mechanisms and precision mechanical systems to join its growing R&D team. This role is ideal for a creative, hands-on mechanical engineer who enjoys ideation, early-stage concept development, and detailed mechanism design, and who is motivated by solving complex engineering challenges at very small scales. You will play a key role in the development of a next-generation adaptive optical platform, working from first principles and early concepts through prototyping, testing, and transition into scalable manufacture. About the Company The company operates at the intersection of ophthalmics, optics, and advanced mechanical engineering, developing novel adaptive lens technologies for applications across AR/VR/XR, machine vision, and next-generation optical systems. Its proprietary adaptive lens technology has generated significant interest from leading global consumer electronics and technology companies. As a result, the business is entering an exciting new phase of growth, expanding its R&D capability and investing in both facilities and talent. The culture is collaborative, technically ambitious, and strongly focused on engineering excellence — an environment where innovative ideas are encouraged, explored, and realised. The Role As a Mechanical Engineer with a focus on micro-mechanisms and precision systems, you will contribute across the full product development lifecycle. The role places strong emphasis on concept generation, mechanism architecture, and detailed mechanical design, alongside hands-on prototyping and testing. You will work on mechanisms at watch-scale and below, helping to define how the system works mechanically as well as how it is manufactured, assembled, and scaled. This is a high-ownership role offering genuine influence over technical direction and design decisions. Key Responsibilities You will: • Generate and develop early-stage concepts for micro-mechanisms and precision systems, exploring multiple design approaches and architectures, • Design micro-mechanisms and precision mechanical assemblies (e.g. bearings, gears, threads, linkages) for optical and opto-mechanical applications, • Translate high-level functional requirements into robust, detailed mechanism designs, • Build, assemble, and test prototypes to validate performance and rapidly iterate designs, • Integrate mechanical systems into complex optical platforms, • Select appropriate materials, balancing performance, reliability, and manufacturability, • Apply DFM/DFA principles and advise on best-practice manufacturing techniques, • Work closely with suppliers and manufacturing partners to realise designs, • Contribute to technical documentation, risk management, and design reviews in a regulated development environment Requirements Education • Degree in Mechanical Engineering, Design Engineering, or equivalent practical experience Essential Experience & Skills • Proven experience taking mechanical products from concept through to production, • Strong capability in ideation, concept development, and mechanism synthesis, • Experience designing precision mechanical systems and/or micro-mechanisms, • A hands-on approach to prototyping, testing, and iterative development, • Solid understanding of manufacturing processes, including:, • Injection moulding and micro-moulding, • Metal stamping and forming, • Metal injection moulding, • Vacuum forming, • Knowledge of joining processes such as:, • Adhesive bonding, • Ultrasonic welding, • Radio-frequency welding, • Heat staking, • Strong materials knowledge, particularly polymers and metals, • Proficiency in CAD (SolidWorks preferred), • Experience working within ISO 13485 or similar regulated design environments Desirable • Competence in GD&T and experience performing tolerance analysis, • Exposure to optics or opto-mechanical design, including alignment or mounting considerations, • Experience with FEA and/or analytical hand calculations, • Ability to translate product requirements into clear engineering specifications, • Experience supporting pilot production and optimising designs for scale-up Why Join? • Work on genuinely novel technology with global impact, • Strong emphasis on creative engineering and early-stage design thinking, • High ownership role with involvement from concept to production, • Collaborative, technically driven culture, • Opportunity to grow with a fast-scaling technology company

An optical technology company based in Oxfordshire is seeking an experienced Mechanical Engineer with a strong background in tooling and fixture design and development to join its growing R&D team. The successful candidate will apply their expertise to design and fabricate first-of-their-kind prototypes for the company’s novel optical platform. This is an exciting opportunity for a hands-on, creative Mechanical Engineer with a strong background in Design for Manufacture and Assembly (DFX) to play a key role in the development of a next-generation adaptive lens technology set to transform the way we see the world. About the Company This company’s expertise sits at the intersection of ophthalmics and optics. They develop novel ophthalmic solutions for use across optical systems, AR/VR/XR, and machine vision applications. Recognised as trusted experts in adaptive lens technology, they partner with leading global consumer electronics and technology companies to develop new solutions that optimise how we see the world. The company has developed a novel adaptive lens system that has the potential to transform visual performance in modern AR/VR/XR technologies. This breakthrough has generated significant interest across the consumer technology sector. As a result, the company is now entering the next phase of its R&D programme, scaling its technical capabilities and seeking talented engineers to join the team. This is an excellent opportunity to join a fast-growing technology company, contribute to cutting-edge R&D, and play a key role in the development of a new technology with global impact. Above all, it is an outstanding place to work, combining innovation, collaboration, and technical excellence. The Role This is an exciting period of investment and growth. The company is scaling its team and facilities to support ambitious R&D activities and is seeking an experienced Mechanical Engineer to design and develop the tooling and fixtures required for the assembly of its brand-new optical platform. You will be a key contributor, working closely with the Design and Production teams to develop critical equipment that supports the assembly of novel prototypes. As this is a completely new optical system, the role requires a high degree of creativity, with responsibility for developing first-of-their-kind assembly equipment and production processes. Key Responsibilities The Mechanical Engineer will: • Design and develop tooling and fixturing, • Provide expertise in Design for Manufacture and Assembly (DFX), • Contribute to the development of novel assembly and production processes, • Liaise with suppliers for the provision and manufacture of parts Requirements Education Essential • Proven experience taking product concepts through to production, including design iteration, refinement, and DFX considerations, • Experience in the design and development of jigs, tooling, and fixtures, • Experience developing novel assembly and production processes, • Solid understanding of:, • Machining processes (e.g. CNC, lathes & milling), • Injection moulding, • Micro-moulding, • Metal stamping and forming, • Metal injection moulding, • Vacuum forming, • Knowledge of common joining processes, including:, • Adhesive bonding, • Ultrasonic welding, • Radio-frequency welding, • Heat staking, • Strong knowledge of materials and their properties, particularly polymers and metals, • Proficiency in CAD (essential), ideally SolidWorks, • Skilled and experienced at using mills and lathes to facilitate machining or modifying tooling and fixtures in-house as required., • A flair for concept generation and ideation and ability to work and iterate designs at a quickly. Desirable • Competence in Geometric Dimensioning & Tolerancing (GD&T), • Experience or exposure to optics or opto-mechanical engineering, including alignment considerations, optical component mounting, or light-path constraints, • Experience taking designs into pilot production and optimising them for scalable manufacture, • Knowledge of, and ability to work to, ISO 13485 (medical device compliance), including documentation, standards adherence, and design-for-risk-management

An innovative optical technology company based in Oxfordshire is seeking an experienced Mechanical Design Engineer to join its expanding R&D team. The successful candidate will bring strong expertise in the hands-on design and development of precision, complex systems, supporting novel research initiatives and contributing directly to the development of a next-generation adaptive lens system. This is a rare opportunity to join a well-funded, highly creative organisation that is poised to redefine the way we see the world. About the Company Operating at the intersection of ophthalmics and advanced optics, the company develops cutting-edge ophthalmic solutions for use across optical systems, AR/VR/XR platforms, and machine vision applications. Widely recognised as leaders in adaptive lens technology, they collaborate with major global consumer electronics and technology brands to create innovative solutions that enhance visual performance. Their proprietary adaptive lens system has the potential to significantly transform visual capability within modern AR/VR/XR technologies. Following strong interest from the consumer technology sector, the company is now entering an exciting new phase of its R&D programme — scaling both its technical capabilities and engineering team to support continued innovation. This is an exceptional opportunity to join a fast-growing technology business, contribute to genuinely cutting-edge development, and play a pivotal role in bringing a globally impactful technology to market. The company offers an outstanding working environment built on innovation, collaboration, and technical excellence. The Role With continued investment and expansion, the company is growing its team and facilities to support ambitious R&D goals. They are seeking an experienced Mechanical Design Engineer with a proven track record in the hands-on design and development of precision products and systems. You will play a central role in advancing the company’s novel lens system, working closely with multidisciplinary teams to take innovative concepts from early-stage development through to production. This role requires someone who is genuinely passionate about detailed, hands-on design work and excited by the challenge of developing precision, small-scale products. Key Responsibilities The Mechanical Design Engineer will: • Design and develop company systems and component parts, • Act as a key interface between analysis and design teams, • Design and develop systems incorporating mechanisms and moving components, • Apply Geometric Dimensioning & Tolerancing (GD&T) and conduct detailed tolerance analysis, • Perform analytical calculations and simulations to support design decisions, • Take a hands-on approach to prototyping — designing, building, and testing to enable rapid iteration, • Provide expert input on materials selection, • Advise on best-practice manufacturing techniques and production readiness Requirements Education Essential • Proven experience taking product concepts through to production, including design iteration, refinement, and design for manufacturing and assembly (DFX) considerations, • Experience designing small but ideally micro-mechanisms, • Solid understanding of:, • Injection moulding, • Micro-moulding, • Metal stamping and forming, • Metal injection moulding, • Vacuum forming, • Knowledge of common joining processes, including:, • Adhesive bonding, • Ultrasonic welding, • Radio-frequency welding, • Heat staking, • Competence in GD&T and proficient in undertaking and documenting tolerance analysis., • Strong knowledge of materials and their properties, particularly polymers and metals, • Proficiency in CAD (essential), ideally SolidWorks Desirable • Experience or exposure to optics or opto-mechanical engineering, including alignment considerations, optical component mounting, or light-path constraints, • Practical experience with Finite Element Analysis (FEA) and/or the ability to perform hand calculations, • Ability to translate product requirements into clear, complete engineering specifications, • A flair for rapid concept generation and ideation, • Experience taking designs into pilot production and optimising them for scalable manufacture, • Knowledge of, and ability to work to, ISO 13485 (medical device compliance), including documentation, standards adherence, and design-for-risk-management

An innovative optical technology company based in Oxfordshire is seeking an experienced Mechanical Systems Engineer to join its growing R&D team. This role will focus on the architecture, integration, and system-level design of a novel adaptive optical platform. You will work across mechanical, optical, and analytical disciplines to ensure that complex mechanical systems, sub-systems, and mechanisms come together into a robust, high-performance product. This is a unique opportunity to contribute to a next-generation lens technology that is set to transform the way we see the world. About the Company This company’s expertise sits at the intersection of ophthalmics and optics. They develop novel ophthalmic solutions for use across optical systems, AR/VR/XR, and machine vision applications. Recognised as trusted experts in adaptive lens technology, they partner with leading global consumer electronics and technology companies to develop new solutions that optimise how we see the world. The company has developed a novel adaptive lens system that has the potential to transform visual performance in modern AR/VR/XR technologies. This breakthrough has generated significant interest across the consumer technology sector. As a result, the company is now entering the next phase of its R&D programme, scaling its technical capabilities and seeking talented engineers to join the team. This is an excellent opportunity to join a fast-growing technology company, contribute to cutting-edge R&D, and play a key role in the development of a new technology with global impact. Above all, it is an outstanding place to work, combining innovation, collaboration, and technical excellence. The Role This is an exciting period of investment and growth. The company is scaling its team and facilities to support ambitious R&D programmes and is seeking a Mechanical Systems Engineer with a strong background in system architecture, integration, and verification. You will take ownership of overseeing the lifecycle of the mechanical systems, ensuring that they integrate seamlessly with one another. Working closely with mechanical design engineers, optical engineers and finite analysis engineers, you will bridge the teams; managing requirements, analysing and mitigating technical risks, and trace the system requirement through to the final product. Ultimately translating the user and stakeholder needs into technical specifications to help deliver well-integrated, reliable products and manufacturing solutions. Key Responsibilities The Mechanical Systems Engineer will: • Define and own the mechanical system architecture for the company’s adaptive lens platform, • Define, document and trace system requirements, from user and stakeholder requirements into clear mechanical specifications and the final product., • Lead the integration of sub-systems, mechanisms, and components into a cohesive mechanical system, • Act as the primary interface between design, analysis, optics, and manufacturing teams, • Ensure system-level considerations are correctly defined, • Identify, analyse and help lead technical mitigations., • Support system verification and validation, including test planning and interpretation of results, • Provide guidance on materials selection and manufacturing strategies at a system level, • Contribute to design reviews and technical decision-making across the programme Requirements Education Essential • Proven experience of taking a holistic view in delivering complex mechanical systems from concept through to production, • Strong understanding of mechanical system architecture, interfaces, and integration, • Proven experience in identifying, analysing, and mitigating technical risks throughout the product development lifecycle (e.g. dFMEA)., • Experience working with precision assemblies containing mechanisms and moving parts, • You will have, and be able to demonstrate, a broad knowledge and experience of manufacturing processes, joining techniques and assembly methods., • Strong knowledge of materials and their properties, particularly polymers and metals, • Proficiency in CAD (essential), ideally SolidWorks, • Experience working within regulated product development environments, ideally ISO 13485, including documentation and design-for-risk-management Desirable • Solid knowledge of tolerance analysis, stack-ups, and GD&T at a system level, • Experience in opto-mechanical systems, including optical alignment, mounting strategies, and sensitivity to tolerances, • Exposure to systems engineering methodologies, including requirements management and verification planning, • Practical experience with FEA or the ability to critically assess analysis outputs, • Experience supporting pilot builds and transition to scalable manufacture, • Ability to balance technical detail with big-picture system thinking, • A flair for problem-solving, concept generation, and structured decision-making

Product Quality Engineer – Medical Devices Location: Kidlington Salary: Highly Negotiable, Dependent on Experience An exciting opportunity to join a growing medical imaging company developing cutting-edge 3D imaging technology. With commercialisation underway in the UK and US, we are expanding our manufacturing capability and seeking a Product Quality Engineer to strengthen the Quality & Regulatory Affairs team. Role Overview The Product Quality Engineer will plan, coordinate, and manage quality assurance and quality control activities across product development, manufacturing, and post-market. This includes developing DHF deliverables, supporting verification/validation, managing non-conformances and CAPAs, and providing compliance guidance to colleagues. The role plays a key part in ensuring adherence to ISO 13485, FDA 21 CFR 820 (transitioning to QMSR), and CE/510k requirements. Key Responsibilities • Lead and support quality engineering activities for medical, veterinary, and non-destructive testing systems., • Contribute to design and manufacturing documentation, ensuring products can be effectively manufactured and tested., • Oversee risk management planning, assessment, and reporting for new and modified products., • Support design transfer, supplier qualification, and quality test method validation., • Generate and maintain quality documentation, including SOPs, work instructions, and inspection procedures., • Manage NCRs, CAPAs, and continuous improvement initiatives., • Collaborate with R&D, suppliers, and manufacturing teams to embed quality throughout the lifecycle., • Provide training and guidance on regulatory compliance and quality standards. Qualifications & Skills • Degree in Science or Engineering, or equivalent experience., • Recognised Quality Management System qualification (e.g., ISO auditor) or similar experience., • Strong knowledge of product development, manufacturing, and quality systems in regulated industries, ideally medical devices., • Familiarity with standards such as ISO 13485, FDA QSR, risk management (FMEA), and medical device cybersecurity., • Skilled in Lean/Six Sigma methods and tools such as Minitab, DOE, and SPC., • Excellent planning, problem-solving, and communication skills, with the ability to work independently and collaboratively. This is a great opportunity to join an innovative scale-up and directly contribute to the delivery of high-quality, safe, and effective products to market.

Overview Pictura Bio is a well-funded University of Oxford spin-out developing a novel diagnostic platform for rapid pathogen detection. Our technology combines fluorescence microscopy with automated image analysis and machine learning to identify pathogens in seconds. The platform is being translated into clinical diagnostic products, initially focused on respiratory infections, with broader applications across infectious disease. Role Purpose The Clinical Validation Lead will be responsible for designing, executing, and overseeing clinical and analytical validation of Pictura Bio’s diagnostic assays. You will lead validation strategy from late-stage development through clinical evaluation, ensuring studies are scientifically robust, regulator-ready, and aligned with the intended clinical use. This role is ideal for someone with hands-on experience validating diagnostic assays in regulated environments, particularly US LDTs, but experience with FDA-cleared/approved, UK, or EU IVD pathways is also highly relevant. You will work closely with assay development, data science, regulatory, and external clinical partners. Major Accountabilities · Lead the design and execution of analytical and clinical validation studies for diagnostic assays · Define validation plans covering precision, accuracy, sensitivity/specificity, LoD, reproducibility, interference, and cross-reactivity · Ensure validation studies are aligned with intended use, clinical claims, and regulatory expectations · Oversee clinical sample selection, handling, and testing in collaboration with partner laboratories and CROs · Support validation of Laboratory Developed Tests (LDTs), particularly within the US regulatory framework · Contribute to validation supporting FDA (e.g. De Novo / 510(k)), UKCA, or CE-IVD pathways where applicable · Review and approve protocols, reports, and data summaries for internal and external use · Work with data science teams to ensure clinical performance metrics and analyses are appropriate and traceable · Interface with regulatory and quality teams to support technical files, submissions, and audits · Manage external stakeholders (clinical sites, reference labs, CROs) involved in validation activities · Clearly communicate validation strategy, results, and risks to senior leadership Ideal Background Education · PhD, MD, PharmD, or MSc in a relevant discipline (e.g. Clinical Sciences, Biomedical Sciences, Molecular Biology, Immunology, Microbiology) Experience · Demonstrated experience clinically validating diagnostic assays · Experience with assays such as immunofluorescence, molecular diagnostics, NGS / optical sequencing (e.g. Illumina), or imaging-based diagnostics · Experience developing or validating US Laboratory Developed Tests (LDTs) is highly desirable · Experience supporting FDA-cleared/approved assays (De Novo, 510(k), PMA) or UK/EU IVD pathways is advantageous · Experience working with clinical samples (e.g. respiratory samples, blood, urine, swabs) · Experience collaborating with hospital labs, reference labs, or CROs Skills · Deep understanding of diagnostic validation principles and study design · Strong knowledge of clinical performance metrics and statistical interpretation · Familiarity with regulatory and quality frameworks (e.g. CLIA, CAP, ISO 13485, ISO 15189) · Ability to translate clinical requirements into practical validation studies · Strong documentation, reporting, and review skills · Excellent communication skills, including interaction with clinicians, regulators, and executives Desirable Personal Attributes · Highly organised and detail-oriented, with a strong quality mindset · Comfortable taking ownership of complex, multi-stakeholder validation programmes · Scientifically rigorous but pragmatic in balancing timelines and regulatory expectations · Confident communicator who can explain validation decisions clearly · Comfortable working in a fast-moving, scaling diagnostics company

ROLE: Senior Quality Engineer LOCATION: Oxford, UK SALARY: £40,000 – £55,000 per annum Overview: We are seeking an experienced and detail-oriented Quality Engineer to join a precision engineering and manufacturing business based in Oxford. The successful candidate will play a key role in ensuring product conformity, process compliance, and continuous improvement across production, inspection, and supplier quality activities. This is a hands-on role requiring strong technical knowledge, effective communication, and a proactive approach to maintaining world-class quality standards. Key Responsibilities: • Act as a key liaison between customers, suppliers, and internal teams on all quality-related matters., • Conduct internal, supplier, and system audits, ensuring compliance with ISO 9001 and customer-specific requirements., • Manage non-conformances, customer complaints, and root cause investigations using structured methods such as 8D and 5 Whys., • Lead operator training in inspection techniques, measurement methods, and equipment usage, including preparation of work instructions., • Oversee the management and calibration of measurement and test equipment, ensuring traceability and accuracy., • Review complex engineering drawings to define appropriate inspection and measurement strategies., • Prepare and maintain inspection and test documentation, reports, and quality control plans., • Support continuous improvement by identifying opportunities to enhance inspection processes, equipment capability, and data analysis., • Participate in project meetings, providing quality input during design, manufacturing, and validation phases., • Conduct supplier audits and performance reviews, providing feedback and improvement recommendations. Skills & Experience: • Minimum of five years’ experience in a Quality Engineering or equivalent role within a manufacturing or engineering environment., • Proficient in Microsoft Office and general PC-based systems., • Strong understanding of inspection methods and measurement techniques, including interpretation of complex mechanical drawings., • Proven ability to train and coach employees in quality and inspection-related topics., • Effective project management and communication skills, with experience liaising directly with customers and suppliers., • Completed Mechanical Engineering Apprenticeship or equivalent qualification. If this role is of interest please apply or email

Project Manager – IVD Development (Start-Up Medical Device) About us Pictura Bio is a rapidly growing biotech company specialising in building instant pathogen tests using advanced microscopy and machine learning. We are a spinout from the University of Oxford, and our technology comes from 6 years of research in the Department of Physics. Pictura Bio is well funded and will provide an opportunity to help develop transformative point of care diagnostic technology. Job description Location: Oxford (Wood Centre for Innovation, Headington) Free onsite parking Salary: Competitive + benefits Hours: Full Time, onsite We’re hiring a proactive, delivery-focused Project Manager to lead the development of an innovative IVD medical device from prototype through to regulated market readiness. In this hands-on role, you will drive integrated plans across engineering, regulatory, and clinical workstreams, ensuring aligned execution in a fast-paced start-up environment. You’ll provide clear visibility on progress, risks, and dependencies while enabling cross-functional teams and external partners to deliver at pace. What You’ll Do • Own and drive cross-functional project plans (software, hardware, regulatory, clinical), • Coordinate internal teams and external partners to ensure aligned delivery, • Lead transition from prototype to regulated device, • Proactively manage risks, dependencies, and key decisions, • Support QMS implementation and promote disciplined documentation and traceability What You Bring • Experience delivering medical devices or IVDs through the full lifecycle, • Strong organisational and stakeholder management skills, • Understanding of regulated development environments (e.g., ISO 13485)

Role: IAM Specialist (Contract) Start: ASAP Security Clearance: Active SC Clearance IR35 Status: Outside IR35 Duration: Initial 3 months Rate: Up to £600 per day Location: Hybrid, approx. 3 days per week on site in Abingdon Overview We are supporting a client delivering a large IAM programme for a public sector end client. They require an experienced IAM Specialist to lead the hands-on implementation and configuration of an Identity Governance and Administration (IGA) platform. You will work within a cyber security team to integrate the IGA solution with Microsoft Entra ID, connect authoritative sources such as HR systems and contractor databases, and build joiner mover leaver processes with automated approval workflows. This is a technical delivery role requiring strong experience in identity lifecycle management and IGA tooling. Key Responsibilities • Implement and configure an IGA platform such as SailPoint, Saviynt, Omada, One Identity or similar, • Integrate the IGA solution with Microsoft Entra ID, • Connect authoritative sources including HR systems and contractor databases, • Design and implement joiner mover leaver processes with automated provisioning and deprovisioning, • Build approval workflows for access requests and role assignments, • Configure application connectors for Active Directory, Entra ID, SaaS and on-prem systems, • Implement access certifications, RBAC models and segregation of duties controls, • Configure SSO and federation using SAML, OAuth 2.0, OpenID Connect and SCIM, • Troubleshoot provisioning, synchronisation and connector issues, • Maintain technical documentation and support audit and compliance activities Essential Skills and Experience • Hands-on delivery of IGA platforms such as SailPoint, Saviynt, Omada, One Identity or similar, • Strong experience integrating with Microsoft Entra ID, • Experience connecting HR systems or other authoritative sources, • Solid understanding of joiner mover leaver automation and identity lifecycle management, • Experience building approval workflows and access request processes, • Strong knowledge of SAML, OAuth 2.0, OpenID Connect and SCIM, • Knowledge of Active Directory, LDAP and hybrid identity, • Working knowledge of ISO 27001 and NIST CSF, • Strong troubleshooting and documentation skills, • Active SC clearance If this sounds suitable and you have active SC Clearance please apply with an up to date CV for immediate consideration.

Overview Pictura Bio is a well-funded University of Oxford spin-out developing a novel diagnostic platform for rapid pathogen detection. Our technology combines fluorescence microscopy with automated image analysis and machine learning to identify pathogens in seconds. The platform is being translated into clinical diagnostic products, initially focused on respiratory infections, with broader applications across infectious disease. Role Purpose You will play a hands-on role in the development, optimisation, and validation of the Pictura Bio assay. Working closely with assay development, imaging, and data science teams, you will support the transition of a research-stage assay into a robust, reproducible diagnostic workflow. This role is fully on-site and laboratory-based, and is suited to a scientist with strong experimental skills, experience in fluorescence microscopy, and an understanding of working within a quality-managed environment. You will be expected to generate high-quality experimental data, document work rigorously, and contribute to assay robustness, reproducibility, and performance verification. Major Accountabilities · Design, execute, and document laboratory experiments supporting assay development · Optimise fluorescence labelling protocols for viruses, bacteria, and other pathogens · Perform fluorescence microscopy imaging using standardised protocols · Support development and refinement of imaging workflows (sample prep, imaging parameters) · Analyse experimental data and contribute to interpretation of assay performance · Verify and validate assay performance (e.g. repeatability, sensitivity, specificity, robustness) · Maintain accurate, detailed laboratory records in line with quality requirements · Contribute to SOPs, protocols, and technical documentation · Work in accordance with company quality systems, policies, and procedures · Collaborate closely with assay, imaging, and software teams to support end-to-end assay development · Undertake other reasonable duties consistent with the role and level Ideal Background Education · BSc or MSc in a relevant discipline (e.g. Biophysics, Biomedical Sciences, Microbiology, Molecular Biology, Bioengineering) · PhD desirable but not essential Experience · Hands-on laboratory experience in assay development or bioanalytical testing · Practical experience with fluorescence microscopy (widefield, epifluorescence, TIRF, or confocal) · Experience working under a Quality Management System (e.g. ISO 13485, ISO 15189, GLP, GxP, or similar) · Experience in an industrial, translational, or regulated laboratory environment is highly desirable Skills · Strong experimental and practical laboratory skills · Good understanding of assay development principles and experimental controls · Familiarity with fluorescence labelling and sample preparation · Ability to follow and improve SOPs and experimental protocols · Strong attention to detail and excellent record-keeping · Comfortable analysing data and reporting results clearly · Familiarity with image analysis software is an advantage · Basic Python or data analysis skills are beneficial but not essential Personal Attributes · Methodical, careful, and data/quality-driven · Comfortable working in a fast-moving, early-stage company · Willing to challenge results constructively and troubleshoot experiments · Collaborative and communicative

Quality Engineer - High-Integrity / Regulated ManufacturingLocation: AbingdonSalary: £48,000 + Training + Progression + Flexitime + Early Friday Finish Are you a Quality Engineer who thrives in complex, regulated environments?Do you enjoy owning NPI, APQP and "right-first-time" delivery from concept through to production? This is a great opportunity to join a highly technical engineering business supplying critical products into safety-led, high-integrity industries. You'll play a key role in ensuring new and existing products meet the highest quality, compliance and traceability standards, while working closely with engineering, manufacturing, suppliers and customers. The RoleYou'll be the quality lead within project teams, supporting New Product Introduction and driving robust quality planning from day one. The focus is on prevention, not firefighting, ensuring products are compliant, traceable and delivered right first time.Key responsibilities include: • Leading APQP and NPI activities from feasibility through to volume production, • Owning PPAP submissions and ensuring manufacturing readiness, • Managing non-conformances, root cause analysis and corrective actions, • Leading internal, external and supplier audits, including special processes, • Ensuring full traceability, lifetime records and material certification, • Supporting process validation, control plans and capability studies, • Quality Engineer within a regulated or high-integrity manufacturing environment, • Strong working knowledge of APQP, PPAP, FMEA, SPC, MSA and Root Cause Analysis, • Experience supporting NPI and transition from prototype to production, • Confident dealing with audits, suppliers and customers, • Able to read engineering drawings and understand manufacturing processes Commutable from: Oxford, Didcot, Radley, Wantage, Grove, Witney, Wallingford, Milton, Sutton Courtenay, Wootton, Marcham, Drayton, Steventon, East Hagbourne, South Moreton, Clifton Hampden, Dorchester-on-Thames, Kennington, Botley, Swindon, Banbury Key words: Nuclear, Regulated Engineering, Supplier Quality, Customer, Special Processes, Welding, NDT, Audit Management, Audits, Launch Readiness Review, Run at Rate, Process Capability, Cp Cpk, Control Plans, Manufacturing Readiness, Engineering Compliance, Quality Assurance Engineer, Quality Systems, ISO 9001, ISO 14001, ISO 45001, ASME, Pressure Equipment, Counterfeit Fraudulent Suspect Items, CFSI, Lifetime Records, Material Certification, BS EN 10204, Continuous Improvement, Lean Manufacturing, Kaizen, Right First Time

Job Description We are looking for an experienced Senior Metrology Technician to join our high precision manufacturing team. You will be responsible for inspecting and checking our machined parts that are required to enable our experimental campaigns for our internal and external customers. You will be helping to build state-of-the-art technology as part of a highly skilled team of scientists and engineers. The role also requires you to work with our manufacturing ISO processes and assist the head of department in developing these. Projects will range from developing pulsed power machines to achieve electro-magnetic launch of projectiles exceeding 20km/s, to complex target design and development. All will require creative approaches in design and manufacturing whilst using various types of tools and materials. Accountabilities and deliverables Inspection of precision components that must meet the required specifications in the agreed timelines. Safe operation of coordinate measuring machines and associated equipment. CMM Programming with data taken from technical drawings and CAD. Planning the most efficient order of work to help keep continuous production. Liaise with designers and technicians to give feedback and assistance. Ensuring that all work meets quality and technical standards. Producing full metrology reports for scientific documentation. Adhere to our manufacturing and ISO processes and procedu...

An innovative and growing medical technology company are recruiting a pro-active and experienced Quality Manager to implement a QMS and ensure compliance with ISO standards, GLP/GMP principles and regulatory requirements while overseeing audit readiness and operational quality across a growing start

Overview Pictura Bio is a well-funded University of Oxford spin-out developing a novel diagnostic platform for rapid pathogen detection. Our technology combines fluorescence microscopy with automated image analysis and machine learning to identify pathogens in seconds. The platform is being translated into clinical diagnostic products, initially focused on respiratory infections, with broader applications across infectious disease. Role Purpose The Clinical Validation Lead will be responsible for designing, executing, and overseeing clinical and analytical validation of Pictura Bio’s diagnostic assays. You will lead validation strategy from late-stage development through clinical evaluation, ensuring studies are scientifically robust, regulator-ready, and aligned with the intended clinical use. This role is ideal for someone with hands-on experience validating diagnostic assays in regulated environments, particularly US LDTs, but experience with FDA-cleared/approved, UK, or EU IVD pathways is also highly relevant. You will work closely with assay development, data science, regulatory, and external clinical partners. Major Accountabilities · Lead the design and execution of analytical and clinical validation studies for diagnostic assays · Define validation plans covering precision, accuracy, sensitivity/specificity, LoD, reproducibility, interference, and cross-reactivity · Ensure validation studies are aligned with intended use, clinical claims, and regulatory expectations · Oversee clinical sample selection, handling, and testing in collaboration with partner laboratories and CROs · Support validation of Laboratory Developed Tests (LDTs), particularly within the US regulatory framework · Contribute to validation supporting FDA (e.g. De Novo / 510(k)), UKCA, or CE-IVD pathways where applicable · Review and approve protocols, reports, and data summaries for internal and external use · Work with data science teams to ensure clinical performance metrics and analyses are appropriate and traceable · Interface with regulatory and quality teams to support technical files, submissions, and audits · Manage external stakeholders (clinical sites, reference labs, CROs) involved in validation activities · Clearly communicate validation strategy, results, and risks to senior leadership Ideal Background Education · PhD, MD, PharmD, or MSc in a relevant discipline (e.g. Clinical Sciences, Biomedical Sciences, Molecular Biology, Immunology, Microbiology) Experience · Demonstrated experience clinically validating diagnostic assays · Experience with assays such as immunofluorescence, molecular diagnostics, NGS / optical sequencing (e.g. Illumina), or imaging-based diagnostics · Experience developing or validating US Laboratory Developed Tests (LDTs) is highly desirable · Experience supporting FDA-cleared/approved assays (De Novo, 510(k), PMA) or UK/EU IVD pathways is advantageous · Experience working with clinical samples (e.g. respiratory samples, blood, urine, swabs) · Experience collaborating with hospital labs, reference labs, or CROs Skills · Deep understanding of diagnostic validation principles and study design · Strong knowledge of clinical performance metrics and statistical interpretation · Familiarity with regulatory and quality frameworks (e.g. CLIA, CAP, ISO 13485, ISO 15189) · Ability to translate clinical requirements into practical validation studies · Strong documentation, reporting, and review skills · Excellent communication skills, including interaction with clinicians, regulators, and executives Desirable Personal Attributes · Highly organised and detail-oriented, with a strong quality mindset · Comfortable taking ownership of complex, multi-stakeholder validation programmes · Scientifically rigorous but pragmatic in balancing timelines and regulatory expectations · Confident communicator who can explain validation decisions clearly · Comfortable working in a fast-moving, scaling diagnostics company

A leading aviation organisation is seeking an experienced Health, Safety & Environment Advisor to take the lead on-site in Oxfordshire.This is a hands-on role where youll drive safety standards, ensure compliance and support ongoing ISO 14001 and ISO 45001 certifications across a busy technical

Job Description Quality Technician, £28,000 - £32,000, Abingdon, Oxfordshire £28,000 - £32,000 depending on experience + pension + 25 days holiday Full-time, permanent position Quality-focused role within a growing medical device manufacturing company operating to ISO 13485 Are you a detail-dr

A leading clinical diagnostics firm is seeking a Senior Quality Specialist to support product quality and Quality Management System processes at their Kidlington location.This role involves guiding the team in compliance, performing audits, and ensuring quality standards are met.Candidates should ha

Production Technician page is loaded## Production Technicianlocations: Abingdon - 141 Park Drivetime type: Full timeposted on: Posted Todayjob requisition id: R0042004is a technology company. Champion a positive safety and environmental culture to satisfy ISO 18001 and ISO 140001 requirement

A leading life sciences company in Kidlington is seeking a Senior Quality Specialist for a 12-month contract.

Supplier Quality Engineer - Medical Devices - Oxford A well‑funded and rapidly growing medical devices company in Oxford is seeking a Supplier Quality Engineer to support the management and development of its supplier base, ensuring that all goods entering and leaving the business meet the required standards. Newton Colmore is recruiting for this role exclusively, so applications must be made directly through us. In this position, you will be responsible for the continual evaluation of existing suppliers, the identification of new suppliers and the ongoing monitoring of supplier performance. You will ensure compliance with ISO 13485, manage CAPAs, apply your quality expertise to design‑for‑manufacture considerations and take on the broader responsibilities expected within a supplier quality function. Ideally, you will be a qualified Lead Auditor with experience working within an ISO 13485 environment. However, we are also open to candidates from other highly regulated sectors such as biotech or aerospace. The technology being manufactured is genuinely industry‑disrupting and has the potential to improve the lives of thousands of people worldwide. The company has secured significant funding due to the success of its device, providing long‑term stability and a strong platform for continued growth. In return, you will receive an excellent starting salary, private healthcare, income protection, life assurance, a pension scheme and a generous holiday allowance, alongside the opportunity to contribute to a transformative medical technology. Interest in this role is expected to be high. If this opportunity aligns with your experience and ambitions, we encourage you to apply promptly. To discuss the position in more detail, contact Andrew Welsh, Director of Medical Devices, Biotech and DeepTech Recruitment at Newton Colmore, on (phone number removed). Alternatively, submit your CV and a member of our team will be in touch to discuss next steps

Senior Administrator Location: Oxford Full Time | Permanent Anglian Recruitment are working with a well-established multidisciplinary consultancy to recruit a Senior Administrator for their Oxford office. This is an excellent opportunity for an organised and proactive professional who enjoys supporting busy project teams and keeping a professional office running efficiently. The successful candidate will provide high-quality administrative support to multidisciplinary teams, ensuring the smooth coordination of projects, documentation, meetings and internal processes. This role would suit someone with a positive, can-do attitude who takes pride in delivering excellent support within a professional environment. Please note: Due to the nature of some projects, successful applicants may be required to undergo security clearance which may include DBS, BPSS, Counter Terrorist Check, Security Check or Developed Vetting. The Role • Provide high quality administrative support to multidisciplinary project teams • Assist with document preparation, formatting and checking using Microsoft Office • Ensure documentation follows company templates, branding and client requirements • Coordinate meetings including preparing agendas, paperwork and meeting minutes • Manage meeting room bookings, refreshments and catering when required • Maintain Outlook calendars for teams and support with diary coordination • Arrange travel and accommodation when required • Manage office documentation including scanning, filing and archiving • Maintain accurate records in line with company procedures and retention policies • Support financial administration including purchase orders, invoices, timesheets and expenses • Update project information and maintain internal management systems and databases • Assist with answering office calls and managing shared inboxes when required • Update and maintain CRM data including client information and project opportunities • Assist with organising client meetings, networking events and marketing campaigns • Support the creation of marketing materials including project profiles, CVs and online content • Work with central teams to ensure compliance with ISO standards and internal procedures • Assist with document control processes using BIM360 (training provided) • Learn and use the company’s practice management software to support invoicing and financial reporting Requirements • Previous experience working in an administrative or office support role • GCSE or equivalent in Maths and English (Grade C or above preferred) • Strong working knowledge of Microsoft Office including Word, Excel and PowerPoint • Excellent organisational skills and attention to detail • Ability to manage multiple tasks and prioritise workload effectively • Professional communication skills and a proactive approach to supporting teams • Knowledge of construction industry terminology is advantageous • Experience with Adobe InDesign or graphic design software would be beneficial but not essential All applications will be treated in the strictest confidence

Supplier Quality Engineer - Medical Devices - Oxford A well‑funded and rapidly growing medical devices company in Oxford is seeking a Supplier Quality Engineer to support the management and development of its supplier base, ensuring that all goods entering and leaving the business meet the required standards. Newton Colmore is recruiting for this role exclusively, so applications must be made directly through us. In this position, you will be responsible for the continual evaluation of existing suppliers, the identification of new suppliers and the ongoing monitoring of supplier performance. You will ensure compliance with ISO 13485, manage CAPAs, apply your quality expertise to design‑for‑manufacture considerations and take on the broader responsibilities expected within a supplier quality function. Ideally, you will be a qualified Lead Auditor with experience working within an ISO 13485 environment. However, we are also open to candidates from other highly regulated sectors such as biotech or aerospace. The technology being manufactured is genuinely industry‑disrupting and has the potential to improve the lives of thousands of people worldwide. The company has secured significant funding due to the success of its device, providing long‑term stability and a strong platform for continued growth. In return, you will receive an excellent starting salary, private healthcare, income protection, life assurance, a pension scheme and a generous holiday allowance, alongside the opportunity to contribute to a transformative medical technology. Interest in this role is expected to be high. If this opportunity aligns with your experience and ambitions, we encourage you to apply promptly. Alternatively, submit your CV and a member of our team will be in touch to discuss next steps.

Quality Engineer - Medical Devices - Oxford There is an excellent opportunity for a Quality Engineer to join a growing and innovative medical devices team in Oxford. Newton Colmore is recruiting for this position exclusively, meaning applications must be made directly through us to be considered. We are seeking someone with a strong background in ISO 13485, CAPA and QMS. Working within an established Quality Assurance team, you will contribute to the ongoing development and maintenance of a medical device that is already improving lives around the world. The technology is electro‑medical in nature, so experience with electronic medical devices would be highly advantageous. While prior experience in medical devices and ISO 13485 is preferred, we are also open to Quality Engineers from biotech, pharmaceutical or other highly regulated industries. In return, you will receive an excellent starting salary, private healthcare, income protection, life assurance, a pension scheme and a generous holiday allowance, alongside the opportunity to work on a transformative medical technology. Interest in this role is expected to be high. If this opportunity aligns with your experience and ambitions, we encourage you to apply promptly. To discuss the position in more detail, contact Andrew Welsh, Director of Medical Devices, Biotech and DeepTech Recruitment at Newton Colmore, on (phone number removed). Alternatively, submit your CV and a member of our team will be in touch to discuss next steps

Lead Assessors wanted TSRN are working with a leading Certification body within the UK who are looking for third party Lead Assessors to cover the London and Surrounding areas. This will be a home based role with ongoing support from their head office. This role would suit Certificated 3rd party Assessors with experience in either ISO 45001, 14001 or 9001. However I am keen to look at other ISO certifications as well. Duties may involve: To undertake visits to clients in accordance with work schedules in an efficient and professional manner within the scope of accreditation. To assess a client’s documented management system to ensure compliance with recognized accreditation standards To prepare and submit a visit report to the Customer Operations Department including recommendations regarding the issue and withdrawal of certificates To provide professional advice to Customer Operations Staff. To ensure that stage 1 and 2 assessments, surveillance activities and recertification Visits comply with the requirements of the Management Systems Manual So if you are passionate about helping business improve their management systems and have third party auditing against ISO 9001, ISO 14001 or ISO 45001 then please contact me on the details below. The package starting salary is between £48k and £55k plus company car, pension, private health care and company benefits.. not to mention ongoing career opportunities

Warehouse / Logistics Team Leader (Manufacturing) Abingdon £33,000-£36,000 + Monday-Friday + Days-based + Progression + Training + Bonus + Overtime + Company Benefits Are you from a Warehouse / Logistics leadership background within Manufacturing or similar looking for a varied, days-based role within a leading manufacturer who are known for looking after their staff in a role offering specialist training to upskill yourself and the chance to continually progress your career? This market leading company are a long-established specialist manufacturer of bespoke products for a broad client base both in the UK and internationally. They are continually moving from strength-to-strength and due to this they are looking to expand their friendly team. This Monday-Friday role will see you overseeing a tight-knit team of operatives in addition to undertaking some occasional hands on work. You will support the logistics manager, oversee stock control, liaise with other departments and carry out associated office based responsibilities as you work Monday-Friday with some optional overtime available to increase earnings. This role would suit a Warehouse Team Leader or similar looking for a local Monday-Friday role within a leading manufacturer offering the chance to increase your earnings and to continually develop your career. The Role: * Oversee and support tight-knit team of operatives * Ensure compliance to ISO accreditations and H&S processes * Monday-Friday days-based role * Liaise closely with other departments and senior leadership The Person: * Warehouse / Logistics Leadership experience * Manufacturing or similar background * Commutable to Didcot Reference number: BBBH24041 If you are interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. We are an equal opportunities employer and welcome applications from all suitable candidates. The salary advertised is a guideline for this position. The offered remuneration will be dependent on the extent of your experience, qualifications, and skill set. Ernest Gordon Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job, you accept the T&C's, Privacy Policy and Disclaimers which can be found at our website

Quality Engineer - Medical Devices - Oxford There is an excellent opportunity for a Quality Engineer to join a growing and innovative medical devices team in Oxford. Newton Colmore is recruiting for this position exclusively, meaning applications must be made directly through us to be considered. We are seeking someone with a strong background in ISO 13485, CAPA and QMS. Working within an established Quality Assurance team, you will contribute to the ongoing development and maintenance of a medical device that is already improving lives around the world. The technology is electro‑medical in nature, so experience with electronic medical devices would be highly advantageous. While prior experience in medical devices and ISO 13485 is preferred, we are also open to Quality Engineers from biotech, pharmaceutical or other highly regulated industries. In return, you will receive an excellent starting salary, private healthcare, income protection, life assurance, a pension scheme and a generous holiday allowance, alongside the opportunity to work on a transformative medical technology. Interest in this role is expected to be high. If this opportunity aligns with your experience and ambitions, we encourage you to apply promptly. Alternatively, submit your CV and a member of our team will be in touch to discuss next steps.

Quality Engineer - High-Integrity / Regulated Manufacturing Location: Abingdon Salary: £60,000 + Training + Progression + Flexitime + Early Friday Finish Are you a Quality Engineer who thrives in complex, regulated environments? Do you enjoy owning NPI, APQP and "right-first-time" delivery from concept through to production? This is a great opportunity to join a highly technical engineering business supplying critical products into safety-led, high-integrity industries. You'll play a key role in ensuring new and existing products meet the highest quality, compliance and traceability standards, while working closely with engineering, manufacturing, suppliers and customers. The Role You'll be the quality lead within project teams, supporting New Product Introduction and driving robust quality planning from day one. The focus is on prevention, not firefighting, ensuring products are compliant, traceable and delivered right first time. Key responsibilities include: Leading APQP and NPI activities from feasibility through to volume production Owning PPAP submissions and ensuring manufacturing readiness Managing non-conformances, root cause analysis and corrective actions Leading internal, external and supplier audits, including special processes Ensuring full traceability, lifetime records and material certification Supporting process validation, control plans and capability studies Acting as a key interface between engineering, manufacturing, suppliers and customersWhat They're Looking For Quality Engineer within a regulated or high-integrity manufacturing environment Strong working knowledge of APQP, PPAP, FMEA, SPC, MSA and Root Cause Analysis Experience supporting NPI and transition from prototype to production Confident dealing with audits, suppliers and customers Able to read engineering drawings and understand manufacturing processes Background in nuclear, defence, aerospace, pressure equipment or similar environments is highly desirableInterested in a confidential conversation? (url removed) (phone number removed) Commutable from: Oxford, Didcot, Radley, Wantage, Grove, Witney, Wallingford, Milton, Sutton Courtenay, Wootton, Marcham, Drayton, Steventon, East Hagbourne, South Moreton, Clifton Hampden, Dorchester-on-Thames, Kennington, Botley, Swindon, Banbury Key words: Nuclear, Regulated Engineering, Supplier Quality, Customer, Special Processes, Welding, NDT, Audit Management, Audits, Launch Readiness Review, Run at Rate, Process Capability, Cp Cpk, Control Plans, Manufacturing Readiness, Engineering Compliance, Quality Assurance Engineer, Quality Systems, ISO 9001, ISO 14001, ISO 45001, ASME, Pressure Equipment, Counterfeit Fraudulent Suspect Items, CFSI, Lifetime Records, Material Certification, BS EN 10204, Continuous Improvement, Lean Manufacturing, Kaizen, Right First Time

HSE Advisor – Utility-Scale Solar Farms & BESS Location: Remote (UK-wide travel as required) Job Type: Permanent Sector: Renewable Energy Salary & Package Up to £45,000 per annum £4,800 car allowance Comprehensive benefits package About the Company We are working in partnership with a leading renewable energy organisation specialising in utility-scale solar farms and battery energy storage systems (BESS). Due to continued growth, they are looking to appoint an HSE Advisor to support the HSE Manager across multiple projects throughout the UK. The Role As HSE Advisor, you will play a key role in supporting both pre-construction and site-based activities, ensuring the highest standards of health, safety, and environmental compliance across renewable energy projects. Key responsibilities include: Developing and implementing HSE policies, procedures, and systems specific to utility-scale solar and BESS projects Providing HSE advice and guidance to project teams, contractors, and stakeholders throughout the project lifecycle Conducting site inspections, audits, and risk assessments, identifying hazards and ensuring compliance with legislation and best practice Supporting incident investigations, reporting, and corrective actions where required Promoting a strong safety culture across all project sites Candidate Requirements To be successful in this role, you will ideally have: A recognised NEBOSH qualification (or equivalent) Working knowledge of ISO 9001, ISO 14001, and ISO 45001 Experience within solar, wind, BESS, or other high-risk construction/engineering environments Strong communication skills and the ability to work collaboratively with multiple project teams A full UK driving licence Package & Benefits Salary up to £45,000 £4,800 car allowance Smartphone and laptop/tablet provided Private Medical Insurance 25 days annual leave + 8 bank holidays Pension scheme Ongoing learning and development opportunities Additional company benefits How to Apply If you are an experienced HSE professional looking to progress your career within the renewable energy sector, we would love to hear from you

Company Profile CBRE is the global leader in real estate services and leverages the industry's most powerful knowledge base to meet the commercial real estate needs of its clients worldwide. Our vision is to be the preeminent, vertically integrated, globally capable real estate service firm. Globally we employ over 70,000 employees and operate in 48 countries. Job Title: SHE Coordinator CBRE Global Workplace Solutions is a leading global provider of integrated facilities and corporate real estate management. We are recruiting a SHE Administrator to join the team located In Oxford RESPONSIBILITIES Responsible for day to day administration of SHE function within the FM Team Site walkarounds/inspections to identify risks and areas of concern and check compliance. Conduct site tours as required Maintain training records, plan training sessions and help develop the training programme including the managing and delivering the site induction programme. Administration of the online DSE training programme and assisting with procurement and issue of specialist equipment. Responsible for maintaining the site emergency response plan, equipment and competency of emergency response team. Track actions from audits, risk assessments and incidents, assist with creating and updating action plans following through to completion. Reviewing and updating site procedures and other documentation. Managing contractors including reviewing RAMS and issuing access permits to work. Develop and deliver programmes, campaigns and activities relating to key risks and controls, including fire safety, health and wellness promotion, environmental awareness and travel safety. Develop and propose SHE communication plan and strategies. Internal and external reporting including compiling environmental and safety statistics. Report on all incidents, assist with investigation to identify corrective actions and share lessons learnt. Monitor and report on agreed KPIs for SHE performance. Management of SHE contracts and expenditure within the FM budget PERSON SPECIFICATION Education Good basic education to GCSE (or equivalent standard), which will include an English and Maths qualification. Education to A-Level/HNC standard / University would be beneficial. Training Very proficient in the use of Outlook, Word, Excel, Access and PowerPoint. Excel skills to include basic functions, v-lookups, etc. NEBOSH Certificate or relevant SHE qualifications/ experience.Experience Experience in FM management environment. Some understanding of ISO accreditations (14001 and 45001) / H&S Regulations.Aptitudes Excellent command of the English language demonstrated through good verbal and written communication. Must be detail conscious, accurate and methodical in approach. Strong organisational and communication skills. Able to work systematically and use own initiative. Able to drive new projects and tasks proactively from start to completion. Able to identify improvements and how processes can be streamlined.Character Must demonstrate a strong sense of customer focus and promote a sense of team spirit and good morale within the office. Reliable, able to complete work within required time frame and manage own deadline requirements. Able to work as part of a multi-disciplinary team, providing support to other areas of the business on occasions, as required. Keen interest in learning and developing within a SHE role Flexibility and willingness to learn

Rubicon Consulting is currently recruiting for Project Quality Lead on a 6 Month Contract, based in Oxfordshire/ Hybrid Working Role Summary • Ensure quality-related project activities and services are implemented efficiently by contractors on the construction site, thus meeting the project-specific quality requirements., • Preparing & reviewing Inspection and Test Plans with subject matter experts., • Continuous improvement by sharing your knowledge through training and regular coaching. This includes - Regular communication with our project management, the site manager, internal specialist departments, document controllers, and the customer's specialist managers., • Ensure that the construction site organization and subcontractors adhere to the project and quality requirements., • Facilitate testing activities on the construction site in accordance with the project quality plan., • Inspect completed work and take any necessary corrective actions., • Identify non-conformances ensuring speedy close outs., • Participate in mitigating negative impacts on the project and developing and implementing solutions., • Support the project team with customer complaints, reporting them, and developing timely solutions., • Drive continuous improvement by sharing knowledge through training and regular coaching. Requirements • Relevant professional experience on construction sites of varying size and complexity., • Previous experience of working in an EPC environment and managing MEICA and civil works., • Exceptional knowledge of quality assurance and quality control., • ISO 9001 Internal Auditor, • IT skills (MS Office, document management)., • H&S experience an advantage, • · Efficient and possess a high degree of technical, interpersonal, and leadership skills., • · Identify and resolve problems early on and work constructively to build positive customer and supplier relationships., • · Communicate your messages coherently and clearly and have the assertiveness necessary for this role., • · Complete the assigned tasks with a high degree of initiative, flexibility, and perseverance, while always adhering to the Code of Conduct., • · Maintain an overview, remain calm, and act in a solution-oriented manner, even in challenging situations. Our Company Rubicon Consulting is a Talent management consultancy which helps you to optimise business performance and competitive advantage by choosing the right people first time

Infinity Employment are currently seeking an experienced Production Inspector to join a busy and fast-paced manufacturing environment to carry out inspection and verification of manufactured parts and assemblies in line with engineering drawings, specifications, and quality requirements. The Production Inspector supports right-first-time manufacture by identifying non-conformances early, applying consistent inspection standards, and working closely with production teams to protect quality, delivery, and compliance. You will be responsible for inspection activities across metallic and composite components, ensuring products meet required engineering and quality standards. This position requires strong CMM experience, specifically using PC-DMIS, within a precision manufacturing environment • 3-month rolling contract opportunity, • £20+ LTD per hour, • Based in Oxford Key Inspection Activities: • Carry out first-off, in-process, and final inspection of metallic, composite, and Siemens parts and assemblies as required., • Inspect components for dimensional accuracy, workmanship, surface finish, and compliance to drawing and specification requirements., • Identify common defects relevant to the process (e.g. composite defects, machining issues, assembly non-conformances)., • Use approved inspection equipment, gauges, templates, and fixtures correctly and safely., • Ensure inspection status is clearly identified, and parts are correctly labelled and segregated., • Knowledge and understanding of these programs would be advantageous. CMM Programming, PCDMIS online and offline, Mitutoyo cosmos, Ziess Calypso, Polyworks, • Excellent understanding of GD&T and technical Drawings Prioritisation & Escalation: • Work to inspection priorities set by the Inspection Team Leader., • Raise urgent inspection requirements or capacity concerns early., • Escalate non-conformances, repeated defects, or unclear requirements through the defined route., • Avoid informal or inconsistent accept/reject decisions outside agreed standards. Quality & Compliance: • Inspect against engineering drawings, specifications, and applicable quality standards (e.g. AS9100, ISO 9001, ISO 13485, Defence)., • Complete inspection records accurately and in a timely manner., • Raise non-conformance reports where required and support investigation activities., • Maintain traceability of parts, materials, and inspection records., • Support internal and external audits when required Teamworking & Communication: • Work as part of a single inspection team across metallics, composites, and Siemens areas., • Communicate clearly with operators, team leaders, and engineers regarding inspection findings., • Provide constructive feedback to support right-first-time manufacture., • Support cross-training and flexible working across inspection areas. Continuous Improvement & Development: • Highlight recurring inspection issues or inefficiencies to the Inspection Team Leader., • Support improvement activities aimed at reducing rework, scrap, and inspection demand., • Actively engage in training and skills development activities., • Maintain personal competence in inspection methods, standards, and equipment Health, Safety & Environment: • Follow all Health, Safety, and Environmental procedures at all times., • Handle materials, components, and inspection equipment safely., • Maintain a clean, organised inspection area in line with 5S expectations. Person Specification: Experience & Background: Experience working in a manufacturing or production environment.Previous inspection or quality experience desirable.Experience inspecting metallic and/or composite components preferred. Skills & Competencies: Ability to read and interpret engineering drawings and specifications. Good attention to detail with a methodical approach to work. Competent in the use of basic inspection and measuring equipment (verniers, micrometers, gauges, templates). Understanding of quality standards and traceability requirements. Willingness to follow agreed priorities and escalation routes. Good communication skills and a team-focused attitude. Strong awareness of Health & Safety requirements

Power BI Overview An exciting opportunity has arisen for an Electrical Design & Documentation Engineer to join a multidisciplinary Electrical Systems team working on advanced industrial and scientific equipment. The team is responsible for the design, installation and commissioning of low-voltage (LV) and high-voltage (HV) pulsed power supplies, control systems, diagnostics and safety systems within a complex engineering environment. In this role, you will support a variety of projects by producing electrical schematics and documentation for both new installations and existing systems. You will collaborate with engineers and technicians to develop solutions, improve processes, and ensure equipment is correctly documented and installed. The scope of work ranges from small electrical assemblies to large and complex machinery and infrastructure installations. Key Responsibilities Create documentation packages in line with company procedures and relevant international standards. Produce complete technical files including Bills of Materials, Load Schedules, Cable Schedules, Terminal Schedules, and supporting OEM manuals and datasheets. Support the Electrical Systems team in documenting both current and future engineering projects. Assist electrical technicians with equipment preparation, assembly and testing, and participate in commissioning activities where required. Collaborate with cross-functional engineering teams to ensure documentation and equipment meet project requirements. Participate in technical reviews to help specify electrical components and control equipment for industrial and scientific automation systems. Produce detailed drawing packages including: Single line diagrams Wiring diagrams Control panel layouts Building floor plans showing cable management and busbar arrangements Update and modify existing designs and drawings in accordance with formal change management procedures. Reverse engineer existing electrical systems to create accurate documentation. Support integration of OEM equipment using manuals, I/O schedules and specification sheets. Produce supporting documentation such as device lists and electrical load and distribution board schedules. Requirements Essential HNC / HND (or equivalent) qualification in an electrical or related engineering discipline. Ability to create and interpret electrical schematics, wiring diagrams, single line diagrams and technical documentation. Experience using electrical test and measurement equipment for troubleshooting and fault finding, with a hands-on approach. Strong understanding of fundamental electrical principles. Experience with electrical design software such as AutoCAD Electrical and Autodesk Vault. Desirable Practical knowledge of electrical design standards such as BS 7671, IEC 60204 and IEC 61439. Awareness of functional safety standards such as ISO 13849 and IEC 61508. Working knowledge of ISO 9001 quality management systems. Familiarity with Microsoft 365 tools including Teams, Planner and OneDrive. Experience with Microsoft Power Platform tools such as Power Automate and Power BI. Rullion celebrates and supports diversity and is committed to ensuring equal opportunities for both employees and applicants

BMS Controls Engineer / £50K - £75K DOE / Oxford / Onsite We're partnered with a leading energy-systems division to recruit a BMS Controls Engineer. This is a hands-on engineering role focused on model-based design and embedded control algorithm development for battery energy storage and related stationary/power applications. The Role You'll develop and deploy embedded control algorithms for Battery Management Systems (BMS) used across energy storage and battery-powered systems. This sits at the intersection of control systems, embedded software and battery technology - ideal for engineers who enjoy end-to-end delivery from models to deployed code. Key Responsibilities Develop control models for embedded targets: SoC/SoH/SoP/SoE estimation, thermal management, cell balancing, voltage/current limits, protection & diagnostics Design, simulate and validate models using MATLAB/Simulink & Stateflow Generate production embedded C code via Simulink Coder / Embedded Coder and deploy to microcontrollers (Infineon XMC, TI C2000, STM32, NXP) Support MIL, SIL and HIL validation workflows Integrate control logic with system, hardware and firmware teams Ensure requirements traceability (ISO 26262 / ASPICE experience beneficial) Debug, analyse and optimise real-time control performance Maintain model/version control using Git or similar tools Requirements B.Sc. or higher in Electrical Engineering, Mechatronics, Control Systems or similar 5+ years' experience with MATLAB/Simulink for control development Hands-on experience with Simulink auto-code generation (Embedded Coder / Simulink Coder) Strong understanding of battery systems and state estimation techniques HIL experience (dSPACE, Typhoon HIL, or equivalent) Working knowledge of CAN and Vector tooling (CANalyzer, CANape, CANoe) Solid control theory, signal processing and embedded systems background Comfortable in a fast-paced product development environment Strong communication, problem solving and organisational skills Desirable UDS diagnostics & battery communication protocols Safety-critical software exposure (ISO 26262, IEC 61508) Scripting for test automation (Python, MATLAB) Familiarity with Git, JIRA, Jenkins or DevOps tooling Basic C/C++ or embedded firmware experience If you're interested then please apply

Embedded Software QA+Test Engineer Oxford (3 days a week) £55,000-£65,000 The Role My client is seeking a talented QA + Test Engineer with expertise in Embedded Software to join their team building cutting-edge assurance systems for AI and UAS/UAV/Drone applications. You will play a crucial role in developing software components that enable safe and reliable operation of AI-enabled robotics and autonomous systems within their product line. Responsibilities Lead the design, development, and implementation of embedded software for SAIF Systems' Runtime Assurance platform across various hardware architectures and real-time operating systems. Ensure compliance with industry standards, regulations, and best practices for safety-critical software development, such as DO-178C, ISO 26262, and IEC 61508. Build configuration and pipeline management Software-in-the-Loop and Hardware-in-the-Loop including automated deployment across multiple platform Integration of different performance testing techniques across multiple types of simulation (gazebo sim, rosbag) Key Skills and Experience Bachelor's or Master's degree in Computer Science, Electrical Engineering, or a related field, or equivalent experience, with a strong focus on embedded systems QA, and software development and/or testing. Experience with one or more CICD pipeline services (Jenkins, CloudBuild, AWS CodePipeline, etc) Experience with infrastructure/Automation techniques (bash, python) Knowledge of source control (git) Experience with at least one test framework (pytest, gtest) Hands-on experience in embedded software testing and QA, with a proven track record in delivering safety-critical systems. The role comes with generous benefits, is 3 days a week onsite and you must be eligible for UK SC clearance. No sponsorship is offered for this role. Please get in touch immediately to be considered

An established multi‑disciplinary property and construction practice is seeking a Practice Information / BIM Manager to lead ISO 19650 implementation and drive BIM Level 2 excellence across the business. This hands‑on role combines standards development, training, quality assurance and content management to improve project delivery and information quality. Key responsibilities Lead ISO 19650 implementation and maintenance across the practice and maintain BIM standards. Develop and maintain documentation including MIDPs, BEPs, IDPs and COBie data schedules. Create and manage Revit/CAD content: templates, families, components and libraries. Deliver training and support in Revit, CAD and BIM processes to multi‑disciplinary teams. Quality control and auditing: spot checks, reporting and continuous improvement. Line manage a central BIM Technician and coordinate cross‑team input. Advise on procurement and licensing with IT and contribute to budget planning. Ensure compliance with sector security requirements and explore AI integration into BIM/CAD workflows. About you Essential: Proven experience with ISO 19650 or equivalent information‑management frameworks; strong Revit and CAD skills; experience producing MIDPs, BEPs, IDPs and COBie schedules; experience delivering training and managing technical staff. Desirable: Defence‑sector security experience; BIM auditing experience; familiarity with AI tools in BIM/CAD; professional membership e.g. RIBA. Benefits Flexible and remote working options. 25 days holiday plus bank holidays and festive shutdown. Competitive pension and health cash plan. Professional membership support, in‑house coaching and mentoring. Cycle to Work, Season Ticket Loan, and other employee schemes. Early finish incentives, volunteering leave and regular social events. If you have proven experience with ISO 19650, strong Revit/CAD skills and a track record of delivering BIM Level 2 projects — and you’re ready to lead standards, training and quality across a busy, multi‑disciplinary practice — apply now! Click apply to send your CV or alternatively contact Joey Waller at Conrad Consulting on (phone number removed) for more details

Senior Administrator - Oxford An award-winning, national multidisciplinary construction consultancy are seeking a Senior Administrator to join their busy Oxford office, supporting the wider practice with a variety of responsibilities. As a Senior Administrator you will also be expected to support the other more junior admins when neccessary. The Senior Administrator Role & Responsibilities As the Senior Administrator, you will be expected to: Provide high-quality administrative support including photocopying, scanning, filing, stationery and supply ordering, and travel arrangements. Prepare, format and check documentation using Microsoft Office, ensuring brand, client and framework compliance. Arrange and coordinate meetings, prepare agendas and minutes, track actions, and manage conference room bookings and refreshments. Manage Outlook calendars, including site access arrangements. Maintain accurate records in line with retention policies, supporting vetting, supply chain processes, audits, invoices, purchase orders, timesheets, expenses and database updates. Support reception duties, including answering calls, managing mailboxes and handling post. Maintain and update the CRM, ensuring accurate client data and compiling marketing contact lists. Support client engagement through organising campaigns, networking and events. Contribute to marketing content including blogs, project profiles, CVs, social media and other promotional materials. Actively participate in team meetings, training and continuous improvement initiatives. Support compliance with ISO standards and accreditations. Assist with document control using BIM360. Operate the Practice Management system 'Manager', including invoicing and supporting monthly financial reportingSenior Administrator Skills Required GCSE Math and English Grade C+ (preferred) Previous construction experience Proficient in Microsoft Office ( Outlook, Excel, Word, Powerpoint) InDesign experience advantageous Extremely organised Timekeeping abilitiesIn Return? Salary: £28,000-£35,000 Flexible working arrangements, including remote working options. 25 days annual leave plus bank holidays, with additional leave over the festive period. Competitive salary with regular market benchmarking and reviews. Employer pension contribution. Health cash plan. Support for professional memberships and ongoing training. Structured development, mentoring and internal coaching. Family-friendly employment policies. Cycle to Work scheme. On-site parking at regional offices. Season ticket loan where applicable. Death in service cover. Early finish incentives linked to company performance. Paid volunteering leave (up to two days per year). Health and mental wellbeing initiatives. Employee referral programme. Regular team and social events fully funded by the business.If you are a Senior Administrator in Oxford looking for a new role, please contact Megan Cole at Brandon James. REF: 21488MC

ISO and Compliance ManagerLocation: Ringwood, Hampshire + non-contractual hybrid home workingSalary: £40,000 - £45,000 DoE + Profit Share + BenefitsHours: 37. The Role Are you an experienced ISO and Compliance Manager, who ensures an organisation maintains full adherence to all statutory, regulato

The role involves managing the Quality Management System in line with ISO 9001 standards and supporting various business functions with quality-related planning.

You'll manage ISO 27001 compliance while collaborating with teams to ensure data security.