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NPI Engineer, Medical Devices, £40,000 - £45,000, OxfordshireAre you an NPI Engineer, Manufacturing Engineer, Process Engineer or Industrialisation Engineer with experience introducing new products and manufacturing processes within the medical device or another highly regulated industry?This is an excellent opportunity to join a growing and innovative medical device engineering company in Abingdon, Oxfordshire, where you will take a leading role in transferring new and modified products from development into controlled manufacture.As NPI Engineer, you will bridge the gap between product development and production, converting engineering and design outputs into robust, repeatable and validated manufacturing processes. You will lead NPI and technology-transfer activities, coordinate cross-functional engineering teams and ensure products are ready for successful production in accordance with ISO 13485 and the company Quality Management System.The Opportunity:£40,000 - £45,000 salary guide + benefits.Join an innovative and growing medical device engineering business.Lead New Product Introduction (NPI) and technology transfer projects.Take products from development through to controlled manufacture.Work across manufacturing engineering, process development, validation and quality.Develop manufacturing processes, equipment, tooling and technical documentationExcellent opportunity for an experienced NPI Engineer, Manufacturing Engineer or Process EngineerThe Role NPI EngineerAs an NPI Engineer, you will be responsible for leading the industrialisation and technology transfer of new and modified medical device products into controlled manufacturing.You will work closely with Engineering, Quality, Production, Supply Chain, Facilities, Validation, suppliers and customers to ensure that products, processes, equipment and documentation are fully prepared for manufacture.Your responsibilities will include:Owning NPI and technology-transfer plans, including deliverables, schedules, readiness criteria, actions and technical decisions.Ensuring that manufacturing processes are robust, controlled and appropriately validated.Ensure that NPI and manufacturing activities meet the required quality and regulatory standards (ISO 13485).Leading cross-functional subject matter experts in translating product, design and customer requirements into repeatable manufacturing processes.Planning engineering trials, pilot builds, validation builds and initial production runs.Identifying and resolving technical gaps before manufacturing release.Assessing whether transferred processes are suitable for the required production volume, equipment, facilities, personnel and environmental controls.Providing hands-on engineering support during initial production until processes are stable and formally transferred to Production.Developing and maintaining manufacturing documentation including process flows, Bills of Materials (BOMs), specifications, work instructions, travellers and inspection methods.Defining manufacturing sequences, critical process parameters, operating limits, acceptance criteria and in-process controls.Specifying and introducing manufacturing equipment, tooling, jigs, fixtures, consumables and measurement equipment.Planning engineering trials, analysing process data and using the results to improve manufacturing processes.Maintaining traceability between product requirements, design outputs, manufacturing processes, risk controls, verification, validation and released documentation.Your Background NPI EngineerWe are looking for an experienced NPI Engineer, Manufacturing Engineer, Process Engineer, Industrialisation Engineer or Technology Transfer Engineer with experience working in a controlled manufacturing environment.You should have:An Engineering degree or equivalent relevant practical engineering experience.Experience within medical devices or another highly regulated industry.Working knowledge of ISO 13485.Previous experience in NPI, New Product Introduction, manufacturing engineering, process development, industrialisation or technology transfer.Experience creating controlled manufacturing documentation.The ability to interpret engineering drawings, specifications and technical data.Experience leading cross-functional technical projects and coordinating subject matter experts.Strong problem-solving and analytical skills.Excellent communication skills and the ability to influence technical decisions across different functions.Experience within medical devices, precision engineering, pharmaceuticals, aerospace, automotive or another highly regulated manufacturing environment may be relevant, provided you have strong NPI and controlled manufacturing experience.Why Apply?This is an excellent opportunity for an experienced NPI Engineer or Manufacturing Engineer to take ownership of the transition of innovative medical device products from development into production.You will have genuine responsibility for NPI, industrialisation, technology transfer, manufacturing process development and validation, rather than simply supporting an established production process.The role offers exposure to the complete journey from engineering and product development through to manufacturing readiness, validation and initial production, making it particularly attractive to an engineer who enjoys solving technical problems and working across multiple disciplines.You will also have the opportunity to develop your experience within the highly regulated medical device industry, working to ISO 13485 and contributing to products where quality, reliability and patient outcomes are critical.This NPI Engineer job is commutable from Oxford, Didcot, Abingdon, Wantage, Witney, Bicester, Aylesbury, Faringdon, Swindon and surrounding areas.To apply, please send your CV to Luke Smith at Euro Projects Recruitment Ltd.Visit the Euro Projects Recruitment website to search our latest permanent, contract and interim vacancies.Please note that if you are not contacted within the next ten days then your application, on this occasion, has not been successful. We thank you for taking the time to apply.This job is posted by Euro Projects Recruitment, a recruitment consultancy specialising in engineering and manufacturing appointments from tool room to boardroom. We combine over 100 years of technical knowledge and recruitment expertise to introduce the best candidates to the best companies. We are passionate about your future and persistent in our efforts to secure you the right job.TPBN1_UKTJ

Production Technician, £26,000 - £28,000, Abingdon, Oxfordshire \n £26,000 - £28,000 depending on experience + pension + 25 days holiday \n Full-time, permanent position. \n Manufacturing role within a growing medical device company \n Are you a hands-on Production Technician, Assembly Operative or Development Technician with experience in a clean, regulated manufacturing environment? \n Your background as a Prod... \n \n \n ZIPC1_UKTJ

Senior/Principal Optical Engineer – Medical Device & Imaging Systems \n \n Background \n Pictura Bio is an innovative MedTech start-up developing a next-generation point-of-care diagnostic platform. Founded in 2021 as a University of Oxford spin-out, we are advancing technology that enables rapid pathogen identification for earlier diagnosis and treatment of patients. \n \n Our platform integrates fluorescence microscopy, electronics, mechanics, fluidics, software, and biological assays into a highly integrated system. Alongside our long-term objective of developing a regulatory-compliant medical diagnostic device, we aim to develop and supply advanced imaging systems and diagnostic assays for external customers. This offers our team the opportunity to work across both commercial instrumentation and next-generation diagnostic development. \n \n Overview of the Role \n You will own the optical development of our instrument platforms, working closely with the engineering and assay teams to translate scientific requirements into robust imaging solutions. Reporting to the Head of Engineering, this role suits an experienced engineer with a strong background in fluorescence microscopy and biological imaging systems who thrives in a multidisciplinary start-up environment. \n \n This is fundamentally an engineering role focused on practical, deliverable systems. We are looking for someone who understands how to develop manufacturable optical systems using commercially available and bespoke components, and who can make sound engineering decisions balancing performance, complexity, cost, and reliability. \n \n You will act as the optical subject matter expert across: \n • Fluorescence microscopy and imaging systems \n • Illumination and detection architectures \n • Optical component selection \n • Optical testing and characterisation \n \n You will ensure that: \n • Optical requirements are clearly defined and informed by system and assay demands. \n • Optical performance is appropriately characterised and verified. \n • Optical designs remain practical, manufacturable, and scalable. \n • Technical decisions are clearly documented and communicated across disciplines. \n \n Key Responsibilities \n Optical Design & Development \n • Own the development and evolution of the platform optical architecture. \n • Translate assay and system requirements into optical specifications. \n • Specify illumination, filtering, and imaging solutions. \n • Perform optical tolerance analysis and tolerance stack-up. \n • Select and evaluate optical components and suppliers. \n • Contribute to future platform developments and technology assessments. \n \n Systems Integration \n • Work closely with assay, mechanical, electronics, and software disciplines. \n • Assess thermal and mechanical impacts on optical performance. \n • Support integration of optical subsystems into complete instruments. \n • Diagnose and resolve cross-disciplinary performance issues. \n • Communicate complex concepts clearly to both technical and non-technical audiences. \n \n Verification & Characterisation \n • Develop optical test methods, characterisation procedures, performance metrics, and acceptance criteria. \n • Support verification activities and root-cause investigations. \n • Ensure optical performance supports overall system requirements. \n \n Quality & Regulatory \n • Contribute optical design records to the Design History File. \n • Support development activities within an ISO 13485-aligned environment. \n • Participate in risk management activities and design reviews. \n • Support future regulatory submissions across key international markets. \n \n \n About You \n You are a practical engineer with strong optical fundamentals and proven experience developing real-world imaging systems. You will likely have: \n • 5+ years' experience in optical engineering or imaging system development, with a minimum 2:1 degree in a related subject or extensive industry exposure \n • Experience working with fluorescence microscopy-based instrumentation. \n • Strong understanding of optics principles, imaging system performance, and optical component selection. \n • Experience with laser systems and other narrowband illumination sources. \n • Proficiency with optical design tools (e.g. Zemax, Code V, OpticStudio). \n • Experience with optical testing, characterisation, and troubleshooting. \n • An appreciation for manufacturability, reliability, and cost-driven design. \n • Strong communication and problem-solving skills. \n • The ability to work effectively within a multidisciplinary engineering team. \n \n Highly Desirable \n • Experience in medical devices, diagnostics, biotechnology, or life sciences. \n • Experience working within an ISO 13485 environment. \n • Familiarity with imaging-based analysis systems. \n • Experience supporting manufacture, calibration, or design transfer activities. \n • Experience in a start-up or rapidly growing technology company. \n \n Benefits \n Alongside a competitive salary, you'll enjoy: \n • Company equity \n • Pension scheme \n • Private healthcare \n • Cycle to work scheme \n • Professional institute subscriptions \n • CPD investment and support \n \n This is an exciting opportunity to join a growing MedTech company at a pivotal stage in its development. You will play a key role in shaping both our commercial imaging systems and the future evolution of a novel diagnostic platform, with the opportunity to grow into a technical leadership position as the company expands

PrecisionLife is helping transform the delivery of healthcare by building the next generation of precision medicine solutions and Mechanostics® tests to improve disease detection, patient triage & outcomes, predict patients’ drug responses, and reduce the cost of delivering effective care. \n We’re a precision medicine company with global ambition and partnerships with some of the largest international healthcare companies and research institutes. We’re headquartered near Oxford, UK, with offices in London, Copenhagen, Warsaw, and Boston, MA. To learn more, visit: https://precisionlife.com/ \n The SVP RA/QA will be responsible for ensuring PrecisionLife’s Mechanostic products meet all IVD and software/AI/SaMD related regulatory and quality requirements for their approval, marketing and lawful commercialization. The role will lead the implementation of ISO13485 and management of the related Quality Management System, the regulatory strategy across EU (IVDR), UK (UKCA/MHRA) and US (FDA, CLIA, LDT, SaMD) markets, and the regulatory and quality interfaces with biopharma partners on companion diagnostic (CDx) programmes (in the future). \n The role will also support the company’s existing information security and privacy management certifications (ISO 27001 and ISO 27701), extending these to cover the company’s handling of personal genomic, clinical and payment data. \n This is a hands-on leadership role in a scaling AI precision medicine company. The successful candidate will balance strategic regulatory direction with implementation and operational delivery — building the function, owning elements of external audits and submissions, and embedding compliance across product, R&D, clinical and commercial teams. \n \n Responsibilities \n Key Responsibilities — Quality \n\n • Own, maintain and continuously improve PrecisionLife ’s Quality Management System to EN ISO 13485:2016, US FDA QMSR (21 CFR 820 transition), CLIA and applicable LDT requirements.\n, • Act as Management Representative in accordance with EN ISO 13485:2016.\n, • Participate in the Management Review process; establish and report QMS performance metrics for the executive team and Board.\n, • Own document control, training records, CAPA, nonconformance, change control, internal audit and supplier audit programmes for product related certifications and regulatory bodies.\n, • Direct selection process, audit and monitoring of external suppliers and manufacturing partners; ensure design, development and production processes meet applicable standards.\n, • Maintain the Design History File / Device Master Record / Technical File / Performance Evaluation File for each device/product.\n, • Lead preparation for, and host, external audits (EU Notified Body, FDA, MHRA, UKAS, biopharma partner audits).\n, • Operationalise risk management to ISO 14971 (with ISO/TR 24971) across the product lifecycle.\n, • Support and enhance the company’s existing ISO 27001 (Information Security Management) and ISO 27701 (Privacy Information Management) certification related activities, including risk assessments, SoA, document control implementation.\n\n \n Key Responsibilities — Regulatory \n\n • Define and execute global regulatory strategy across EU IVDR, UK (UKCA / MHRA), US (FDA 510(k), De Novo, PMA, CLIA, LDT) and other priority markets.\n, • Act as, or designate and oversee, the Person Responsible for Regulatory Compliance (PRRC) under IVDR Article 15.\n, • Lead product related regulatory submissions, certificate renewals, technical documentation and responses to deficiencies; own Notified Body relationship and capacity planning.\n, • Develop and own the regulatory pathway for AI/ML-enabled SaMD products, including FDA AI/ML guidance, Good Machine Learning Practice (GMLP), Predetermined Change Control Plans, IMDRF SaMD framework and the EU AI Act (high-risk medical AI).\n, • Own post-market surveillance regulatory oversight, PMS plans, PSURs, vigilance, FSCA and incident reporting under IVDR and FDA MDR.\n, • Own software lifecycle compliance oversight: IEC 62304 and IEC 82304.\n, • Own labelling, IFU, packaging and storage regulatory requirements across markets.\n, • Work with the Company Senior Management Team to provide clinical study regulatory oversight: Performance Evaluation Plan, scientific validity, analytical performance, clinical performance, PER, PMPF.\n, • Support and collaborate with the team on topics of cybersecurity regulatory requirements: IEC 81001-5-1, FDA premarket cybersecurity guidance, SBOM.\n, • Provide strategic regulatory input across the product lifecycle to the CPO, CEO, CTO, CBO and Board; brief and present to regulators and Notified Bodies.\n, • Monitor evolving regulation across all target markets and translate into actionable internal guidance.\n\n \n Key Responsibilities — Data Governance & Cross-Functional \n\n • Partner with the DPO and ISO 27001 & ISO 27701 Committee Management Team on Data Security and GDPR compliance for genomic and special-category data, including DPIAs, international transfers and data subject rights.\n, • Embed quality and regulatory thinking into Product, R&D, Clinical and Commercial functions; act as the trusted regulatory voice in early product decisions.\n, • Represent RA/QA in biopharma partner due diligence, CDx co-development agreements and regulatory interactions.\n, • Other duties as required from time to time by the Management team\n\n \n Key Requirements \n\n • Degree in a life science, engineering, computer science or related discipline. PhD or RAC (Regulatory Affairs Certification) preferred but not essential where equivalent senior operational experience is demonstrated.\n, • ISO 13485 accreditation and audit experience\n, • Working knowledge of ISO 14971, IEC 62304, IEC 82304, ISO 15189 and IEC 81001-5-1.\n, • Working knowledge of ISO 27001 and ISO 27701\n\n \n Key Attributes \n\n • Minimum 10 years’ RA/QA experience in IVD, medical device or diagnostics, including at least 3 years in a leadership role.\n, • Demonstrated success obtaining regulatory approval for SaMD-based IVDs under IVDR (CE mark) and US frameworks (CLIA, LDT, and ideally 510(k) or De Novo).\n, • Experience meeting the criteria of, or directly supporting, an IVDR Article 15 PRRC.\n, • Experience implementing and maintaining a QMS in a scale-up or start-up environment — not a large-corporate-only background.\n, • Experience with AI/ML-enabled medical software is strongly preferred.\n, • Strong internal and external audit experience (hosting and conducting).\n, • Prior medical device manufacturing or contract-manufacturer oversight experience.\n, • Excellent communication skills, both verbal and written, including for submissions, technical documentation, regulator correspondence.\n, • Pragmatic, commercially aware, comfortable challenging at executive level.\n, • Able to work effectively to tight deadlines within a collaborative team-orientated environment using sound judgement in decision-making.\n, • Organised and detail-oriented, being able to prioritise and perform multiple tasks effectively and concurrently.\n\n \n Year-One Success Measures (indicative) \n\n • Establish ISO 13485 certification but scaled appropriately for current product mix.\n, • LDT route(s) operational to support PrecisionLife ’s first consumer product launches in the US and EU — CLIA/CAP-certified lab partner qualified, analytical and clinical validation documentation in place, regulatory file complete and EU/MHRA lab strategy.\n, • First consumer launch product(s) shipped with full RA/QA sign-off on labelling, IFU, claims, consent flows, complaint handling and customer-facing materials.\n, • FDA LDT Final Rule phase-out compliance plan in place and on schedule; pre-submission engagement initiated for products on a path to 510(k) / De Novo.\n, • Support completion of consumer-scale privacy and data flows validated under GDPR, ISO 27701 and applicable US state genomic privacy requirements.\n, • PMS, vigilance, complaint handling and CAPA systems operational at consumer scale with measurable KPIs.\n, • RA/QA function appropriately resourced and embedded in product development governance.\n\n \n What We Offer \n\n • Competitive salary with performance related bonuses\n, • Stock Options (subject to qualifying)\n, • Company pension scheme\n, • Life Assurance/Death in Service Insurance (subject to qualifying)\n, • Private Healthcare Scheme (subject to qualifying)\n, • Flexible-Hybrid working pattern model to allow for flexibly between remote and office working\n, • 25 days annual leave (pro rata) (increasing to equivalent of 28 days hols/annum on completion 3 years of service)\n, • Access to substantial number of courses and training events\n, • Excellent career development opportunities in a fast-growing international organisation \n\n \n Right to Work \n Employment is subject to verification of identity, qualifications and the legal right to work in the United Kingdom. Successful candidates will be required to provide appropriate documentation as part of our pre-employment screening process. \n \n PrecisionLife reserves the right to amend, withdraw or close this vacancy at any time without notice. We may close the application process earlier than the advertised closing date if a sufficient number of suitable applications are received. Early application is therefore encouraged. \n The information contained in this advertisement is intended to provide an overview of the role and does not form part of any contract of employment. The duties, responsibilities and requirements described may be amended from time to time to meet business needs. \n Any offer of employment will be subject to satisfactory completion of pre-employment checks. \n \n Data Privacy \n By submitting an application, you acknowledge that your personal data will be processed for recruitment purposes in accordance with our Privacy Policy and applicable data protection legislation, including the UK GDPR, EU GDPR and the Data Protection Act 2018. \n For information on how we collect, use and protect your personal information, please view our Privacy Policy: \n https://precisionlife.com/privacy-policy \n If you have questions regarding data protection, please contact: GDPR@precisionlife.com

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

This is an excellent opportunity to join a growing and innovative medical device engineering company in Oxfordshire, where you will play a hands-on role in the design, development, prototyping, testing and low-volume manufacture of innovative medical devices. Are you a Development Engineer, Design E

The Opportunity This is an exciting time to join an established and internationally respected medical device company with a long history of developing and producing highly regarded medical equipment.Now part of a larger international medical technology group, the business is entering an important p

Medical Device Development Engineer, £38,000 - £42,000, Oxfordshire Are you a Development Engineer, Design Engineer, Mechanical Engineer or Product Development Engineer looking to build your career within the medical device sector? This is an excellent opportunity to join a growing and

Manufacturing role within a growing medical device company Are you a hands-on Production Technician, Assembly Operative or Development Technician with experience in a clean, regulated manufacturing environment? Your background as a Production Technician: • Experience working with small compon

A leading medical device firm in Oxford is seeking a Director of Quality Assurance to guide the quality strategy and operations for their structural heart portfolio. The successful candidate will ensure alignment with regulatory standards and lead continuous improvement across production. Required skills include senior leadership in quality assurance and a strong background in cardiovascular implants. This is a critical role to support the company's mission to advance lifesaving cardiovascular solutions. #J-18808-Ljbffr

📍 Oxford, United Kingdom | Leadership across UK and EU operations | Competitive executive package with strategic growth scope I am supporting an established cardiovascular company advancing next generation structural heart therapies that aim to improve long term outcomes for patients with complex valve issues. As Director of Quality Assurance and Operations, you will guide the quality strategy and operational performance for the structural heart portfolio. You will oversee the quality management system, ensure alignment with UK and international regulatory expectations and lead continuous improvement across production, supplier oversight and product lifecycle activities. The role is highly visible, partnering closely with R&D, regulatory and clinical teams to secure reliable product delivery and support sustained growth. • Senior leadership experience in medical device Quality Assurance and Operations, • Strong background in structural heart or cardiovascular implants, • Expertise with ISO 13485, ISO 14971, EU MDR and relevant UK regulatory requirements, • Demonstrated success managing manufacturing partners, suppliers and operational systems, • Clear communication with influential cross functional leadership skills This is an exceptional opportunity to shape quality and operational excellence within a company committed to advancing lifesaving cardiovascular solutions. 📩 Contact hugh.cross@skillsalliance.com for more information. • Seniority level: Not Applicable, • Employment type: Full-time, • Job function: Quality Assurance, • Industries: Medical Equipment Manufacturing #J-18808-Ljbffr

This job is with VoCoVo, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. VoCoVo specialises in innovative communication solutions tailored for businesses, particularly within the retail sector. Our flagship products are designed to create a connected store experience, facilitating seamless communication among retail staff to enhance efficiency and elevate customer service. We empower teams to collaborate effortlessly and achieve their retail goals. You've probably already seen us in action, we're trusted by Tesco, Asda, Dunelm and Iceland, just to name a few. With over 1 million users across more than 42,000 locations in 39+ countries, and recognition as one of the top 100 best small-to-medium size businesses to work for, join us on our journey! Role Overview VoCoVo's Platform Engineering department forms the technical foundation on which our entire product is built. Spanning cloud infrastructure, developer tooling, messaging and connectivity services, cloud application scalability and our on-premise edge device platform, it is increasingly critical to our growth. As we scale, Platform Engineering requires a dedicated product function to match its growing impact. Working closely with the Head of Architecture & Platform and Technical Leads, you will embed platform engineering within the existing product operating model, adapting it where necessary to meet the unique needs of platform teams. You'll develop and maintain a roadmap that communicates platform investment in outcome-focused terms, provide the visibility internal teams need to understand dependencies and priorities, and ensure platform strategy is clearly understood across the organisation. This is a new role with significant opportunity to shape how platform engineering engages with the wider product organisation and demonstrates its value. This role would suit someone who builds trust through thoughtful questioning, brings clarity to the what and why, and treats internal product and delivery teams as the customers they are, focusing on understanding needs and outcomes rather than defining technical solutions. Please note, to apply for this position you must be based in the UK and have the legal right to work in the UK. This is a hybrid remote position, we're looking for someone who is able to travel once per week, this may be to our office (Shipton-under-Wychwood or Cheltenham) or on customer visits. What we're looking for Excellent product management foundations, with experience in technical B2B environments. Proven experience of working alongside or embedded in platform, infrastructure or enablement teams, alongside an understanding of how these differ from stream-aligned feature teams and what it takes to earn their trust. Strong levels of technical literacy, you are able to engage fluently in platform, infrastructure & architectural conversations, without the need to be an engineer. You have a strong background in translating technically complex work into outcome-focused roadmaps, epics and communications. An internal customer mindset, with the ability to surface and represent the needs of product and delivery teams in platform planning. You are comfortable restructuring technically-framed Jira backlogs into outcome-driven artefacts that non-engineers can understand. The ability to move at pace - navigating tight timelines and strong opinions, you are also able to confidently and respectfully challenge when work risks drifting from outcomes. Excellent communication skills, including experience of presenting technical roadmaps and investment cases to senior leadership. "Nice to have" skills Familiarity with Team Topologies or similar thinking about platform vs stream-aligned team dynamics. Exposure to messaging infrastructure, IoT platforms, edge computing, cloud-native architecture or infrastructure security. Experience introducing product practices into engineering teams that have previously operated without them. Prior experience in a scale-up environment where delivery processes are still maturing. What you'll do Own and rebuild the platform roadmap, transforming a backlog of technical tickets into a structured, outcome-driven plan, legible across VoCoVo. Act as the voice of internal customers, ensuring the needs of product and delivery teams are visible to platform engineers, and platform plans and timelines are visible to the wider business. Work with Platform Technical Leads and Delivery to surface and communicate dependencies in a format that supports proactive planning across stream-aligned teams. Shape outcome-focused artefacts such as epics, initiative briefs and roadmap narratives to provide documented context and value without prescribing the technical solution. Facilitate structured prioritisation across the platform teams, balancing reliability work, strategic investment and internal requests. Define and track meaningful KPIs for platform performance - availability, developer experience and adoption of platform capabilities. Run structured discovery with internal teams to understand what they need from the platform, surfacing unstated constraints and upcoming dependencies. Partner with the Head of Architecture and Platform to establish a sustainable product operating model, freeing engineering leadership for technical strategy and critical escalations. What does success look like? 0-6 months Trusted working relationships have been established with the platform Technical Leads and the Head of Architecture & Platform, and each team's priorities and constraints are understood. You've actively connected with the wider PM community and product-facing teams; understanding their platform dependencies and pain points firsthand. Backlogs and the short-term roadmap tell a story. Epics have outcomes, teams have context and engineering effort connects to visible value. 6-12 months A platform roadmap that engineers, product managers and leadership all understand. Platform capabilities are adopted effectively by feature teams because they are well-communicated and well-documented. Platform Engineering dependencies are visible, information flows freely between platform and product teams, and silos have reduced meaningfully. Salary £60,000 - £65,000 Benefits 25 Days Holiday + Bank Holidays (increases with years of service) Option to buy or sell 5 days holiday each year Sick Pay - 8 weeks full pay, 4 weeks half pay Life Assurance - (4 times basic pay) Private Medical Insurance Employee Assistance Programmes (EAP) Cycle2Work Scheme Electric car green salary sacrifice scheme Enhanced Maternity & Paternity package Child Care Scheme Training & development opportunities Company organised events Pension (Royal London Group) 5% employer contribution matched Apple MacBook, Wireless Magic Mouse and Keyboard, monitor and headphones Diversity and Inclusion At VoCoVo, we are dedicated to fostering a diverse and inclusive workplace where everyone feels valued, respected, and empowered to thrive. We welcome applications from individuals of all backgrounds and experiences. Our commitment is to create an environment that champions equity, innovation, and collaboration, ensuring all team members can flourish. Join us in shaping the future together. We are also committed to ensuring an inclusive recruitment process, so please let us know if you need any reasonable adjustments at any stage. Company Values Embracing VoCoVo's 'VOICE' Values is important to us, shaping our collaborative and innovative culture. VALUED Our Colleagues, Customers, and Stakeholders are valued; treated with respect, empathy, and operate with honesty and integrity ONE TEAM Collaboration of all for VoCoVo's happiness and success INNOVATION Our products are constantly evolving to tackle the pain points of retailers across the globe CUSTOMER FOCUSED Our customers love VoCoVo at every level, every interaction with us is frictionless, and we are integral to their operations EMPOWERED Our people are empowered to do the right thing and make decisions without loads of red tape If you feel this could be the right fit, apply now!

Role: Senior CNC Technician Location: Oxford Salary: Up to £41,000 depending on experience Our client is looking for a skilled Senior CNC Technician to join a specialist mechanical workshop supporting advanced scientific research and development activities. As Senior CNC Technician, you will play a key role in delivering high-quality engineering support across a wide range of activities. The position combines hands-on machining, CNC programming, mechanical design support, equipment maintenance, and technical leadership. You will be responsible for producing precision-engineered components, advising mechanical design solutions, supporting workshop operations, and mentoring junior team members. Responsibilities include: Operate a full range of manual machine tools, including lathes, milling machines, drills, saws, grinders, and sheet metal equipment. Program, set up, and operate CNC machinery to manufacture high-precision components and complex assemblies. Manufacture, assemble, fit, and test bespoke mechanical equipment and instrumentation. Install, modify, maintain, and repair specialist equipment. Produce and interpret detailed engineering and mechanical drawings. Provide technical expertise and practical solutions to complex engineering challenges. Collaborate closely with colleagues and project stakeholders to deliver successful outcomes. Train, mentor, and supervise junior technical staff, particularly in CNC machining and design practices. Maintain high standards of workshop safety, housekeeping, and compliance. Act as a key technical point of contact, communicating engineering concepts clearly to non-engineering stakeholders when required. Skills and Experience: Formal qualification in a relevant engineering discipline (e.g. City & Guilds, BTEC, HNC or equivalent). Completed recognised engineering apprenticeship. Significant experience in high-precision machining within a research, laboratory, scientific, aerospace, defence, medical device, or advanced manufacturing environment. Extensive experience operating and programming CNC machine tools. Strong manual machining skills. Experience using CAD software to create and modify components and assemblies for manufacture. Ability to read, interpret, and produce detailed engineering drawings. Excellent problem-solving and fault-finding skills. Ability to communicate complex technical information clearly and effectively. Experience training, mentoring, or supervising junior staff.WR Engineering are the #1 recruitment partner for engineering, manufacturing & technical sales jobs. We recruit for permanent jobs UK wide. WR is acting as an Employment Agency in relation to this vacancy

MICROFLUIDICS ENGINEER Location: Oxford Reporting to: COO / CPO Employment: Full time, permanent Level: Commensurate with experience Sector: Medical Devices / IVD, early stage startup Working arrangement: On site ABOUT THE COMPANY Our client is a medical device company developing a culture free in vitro diagnostic system for rapid bacterial identification and antimicrobial susceptibility testing directly from whole blood. Their technology combines microfluidic sample preparation, Raman spectroscopy, a growing Raman spectra database, and machine learning driven analysis to produce clinically actionable results far faster than conventional blood culture methods. The technology has performed strongly in laboratory validation, and the company is now progressing through a prototyping and pilot study phase, with regulatory submissions planned under FDA and EU IVDR routes. Microfluidics sits at the heart of the platform, taking whole blood and delivering clean, concentrated, viable cells to the optical system. The successful candidate will join a small, closely knit microfluidics team and will have a genuine, lasting influence on how the sample preparation technology is designed, de risked, and manufactured at scale. THE ROLE This role covers the design and development of microfluidic sample preparation systems used to process whole blood for the diagnostic platform. The company is looking for a hands on engineer to join the microfluidics team, working across the full lifecycle from early stage concept prototyping through to designing for scaled up, regulated manufacture. The position spans bacterial identification (ID) and antimicrobial susceptibility testing (AST) assays as well as emerging fungal applications, and sits at the intersection of microfluidics, fluid mechanics, and practical engineering. You will contribute across design, prototyping, experimental testing, manufacturing transfer, and scale up, taking genuine ownership of the subsystems you work on. KEY RESPONSIBILITIES • Contribute to the design and optimisation of microfluidic devices and flow systems across bacterial ID, AST, and fungal applications, • Design, build, and test prototypes, including experimental validation using biological samples, • Plan and run structured experiments and characterisation studies, including design of experiments, to quantify performance and process robustness, • Analyse system performance and troubleshoot fluidic behaviour, using data to inform design decisions, • Develop and qualify cartridge sealing, bonding, and surface treatment strategies, working with internal teams and external partners, • Support improvements to the robustness, reliability, and scalability of devices, • Design for manufacture and scale up, translating prototypes into robust, high yield designs suited to volume replication routes, • Liaise with external fabrication and manufacturing partners, • Take ownership of specific subsystems or experiments from concept through to testing and iteration, • Balance engineering trade offs between performance, manufacturability, and cost, • Operate within the QMS, moving between rapid prototyping and regulated product development, • Translate overall system and product requirements into sub system requirements, and develop microfluidic systems that meet them, • Ensure engineering concepts are grounded in biological reality, working closely with the scientific team, • Plan, capture, and record design rationale, protocols, and results in clear engineering documentation to support verification, validation, and regulatory submission REQUIREMENTS Essential • Degree in engineering, physics, or a related quantitative discipline, or equivalent practical experience, • Strong fundamentals in fluid mechanics or transport phenomena, • Proven hands on experience with experimental systems or prototyping, including designing, building, and testing physical devices, fluidic systems, or experimental hardware, ideally in a commercial setting, • Ability to work independently, prioritise in a fast moving startup environment, and communicate concepts clearly to colleagues from other disciplines, • Confidence integrating into a multidisciplinary team of scientists, engineers, and clinicians, • A pragmatic problem solver, open to constructive challenge, with a continuous improvement mindset Note: A combination of all or most of these traits would qualify someone for the top end of the salary banding. Desirable • Experience with microfluidics, lab on chip systems, or small scale fluid systems, • Familiarity with CAD, ideally Solidworks, • Experience scaling microfluidic systems for high volume manufacture, • Familiarity with microfabrication and replication techniques and the tolerances they impose, • Experience with surface functionalisation, bonding, and sealing of polymers, • Experience handling biological samples such as blood or cell suspensions, with associated safety practice, • Familiarity with design of experiments (DOE) and statistical analysis of test data, • Experience developing microfluidic devices coupled with optical detection and analytical workflows, • Working knowledge of one or more of ISO 13485:2016, ISO 14971, EU IVDR, and FDA 21 CFR Part 820, • Experience in an early stage startup or spin out environment experiencing rapid growth WHAT'S ON OFFER • The opportunity to own core microfluidics technology at a company delivering genuine translational impact in antimicrobial resistance diagnostics, • A broad, hands on remit spanning rapid prototyping through to manufacture, with real influence over design direction, • Direct access to and collaboration with the founding team and scientific leadership, • Competitive salary, commensurate with experience and company stage HOW TO APPLY For a confidential discussion about this role, please contact Max Marcus at Platform Recruitment. Seniority Level Mid-Senior level Industry • Medical Equipment Manufacturing Employment Type Full-time Job Functions • Engineering Skills • Part 820, • On Site, • Medical Devices, • Translation, • 21 CFR, • SOLIDWORKS, • Databases, • Direct Access, • CFR

Quantum is now, and it's built here. Oxford Ionics, now part of IonQ, is pioneering the next generation of quantum computing. Using our world-leading trapped-ion technology, we're building the most powerful, accurate and reliable quantum systems to tackle problems that today's supercomputers cannot solve. Joining Oxford Ionics means becoming part of a global IonQ team that is transforming the future of quantum technology - faster, at scale, and with real world impact. What to expect: We are looking for a Staff FPGA Engineer to join our FPGA Team at IonQ. In this role, you will be responsible for designing and developing FPGA features, contributing to the team's mission of delivering best in class control systems. You'll play an important part in shaping hardware that supports our work in building the world's most advanced quantum systems. What you'll be responsible for: In this position, you will work on designing, developing and testing RTL modules, supporting the effective delivery of real-time control logic for quantum control systems. You'll have the opportunity to own, architect, and develop critical control functions, contributing directly to the success of operating a quantum computer. Work independently to design and implement FPGA based signal processing and control functions and develop functional block specifications based on system level requirements Perform logic design using Vivado (Verilog or VHDL, IP Catalog, and Block Design as well as perform logic simulation/verification using simulation/verification software Simulate signal processing and control algorithms in software Implement and test firmware for high speed waveform generation and digital control loops. Write test procedures, perform unit and system level testing and debug, document test resultsRequirements To be successful, you will need strong FPGA design and verification experience and experience working on complex systems. You will have experience in development, verification, and debugging of FPGA-based systems, with a strong focus on signal processing and high-performance embedded solutions. We're looking for someone who can work cross-functionally to gather requirements, architect, design, and contribute effectively within a fast-moving, highly technical team. To be successful in this position, you will need a Bachelor's degree in Electrical Engineering, Physics, Mathematics, or a related technical field, along with at least 10 years of hands-on FPGA development experience. You should have detailed knowledge of FPGA-based signal processing techniques including DDC/DUC, DDS, and FIR/IIR filters, as well as strong experience in FPGA verification and SystemVerilog development. We're looking for someone who is fluent in modelling and simulation using Python and/or MATLAB/Simulink, with practical experience in code coverage, functional coverage, and industry-standard verification tools such as Synopsys, Cadence, and ModelSim. Familiarity with Xilinx Ultrascale+ MPSoC devices and common peripheral interfaces including SPI, I2C, UART, and USB is also essential. You will also be confident using JTAG and Integrated Logic Analyzers for system debugging and proficient with complex laboratory equipment such as signal generators, oscilloscopes, and spectrum analyzers. You'd be a great fit with: Experience with ASIC design and tapeout process Experience implementing digital control (PID, feedforward, MIMO) algorithms in FPGA firmware Prior experience with high speed interface design and verification including ADC/DAC (DDR and JESD204B), DDR3/4 MIG, and 10 Gigabit Ethernet Working knowledge of embedded linux and linux device drivers Experience using GitLab for automated firmware build and validation Experience working closely with board design and software development teamsBenefits Be part of a team that's shaping the future of quantum. We offer more than just a role, you'll join a world class community of scientists, engineers and innovators working to unlock the full potential of quantum computing. We offer a range of benefits, including opportunities to further your career alongside industry leaders, a competitive salary with IonQ stock options, an annual performance bonus, generous annual leave, flexible hybrid working, private medical and dental insurance for you and your family, and much more. Join us and be part of the future of quantum computing. We're proud to be an equal opportunity employer and welcome applicants from all backgrounds

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