Medical Technology Jobs

Johnson & Johnson MedTech · High Wycombe

Oversees the end-to-end process for internal and external clinical data sharing requests, ensuring compliance with privacy standards and procedural requirements. Supervises vendors handling data anonymization and synthetization, and acts as the primary contact for YODA Project requests, securing clinical team approvals. Supports external research teams using clinical study data and leads cross-functional projects within a matrix organization.

Johnson & Johnson MedTech · Beerse, Belgium

Strategic lead for modernising the Clinical Risk Management digital and data landscape, defining roadmap, governance, investment cases and value measures. Partners with CRM leadership, RDQ, technology and external vendors, while a Manager handles day-to-day process optimisation and digital administration.

Smith & Nephew · Wrexham

Field-based clinical sales role covering North Wales and the Midlands, acting as the go-to expert for complex wound care within the Advanced Wound Management portfolio. Involves hands-on clinical support, education and relationship building with community healthcare professionals, guiding decision makers and strengthening advocacy for therapies across the territory.

Medtronic · Eindhoven, Netherlands · €149,600 – €224,400 pa

Leads commercial growth and adoption of connected care and digital health solutions across Western European hospital systems, negotiating multi-year enterprise partnerships and guiding product launches. Manages a growing team and works with clinical, IT and executive stakeholders on interoperability, data integration and remote monitoring. Remote with around 70% regional travel.

Platform Recruitment · Royston · £45,000 – £50,000 pa

Develops high-quality, well-documented embedded software in C/C++ on RTOS or bare metal, working across the full lifecycle from requirements capture to verification and release. Sits in multi-disciplinary teams with client-facing communication and significant ownership of design decisions on medical devices.

Computer Futures · London · £75,000 – £85,000 pa

Drive software safety activities across the product lifecycle for software-based medical devices, including hazard analysis, risk assessments and safety documentation. Work with Software, Quality, Regulatory and Product Development teams to ensure compliance with standards such as ISO 14971 and IEC 62304, and support verification, validation and software risk management.

Talentmark · Wrexham · £22 – £29 ph

Translate business requirements into user stories and acceptance criteria, working with a scrum master on story sizing and risk analysis. Participate in release and sprint planning, backlog grooming and sprint reviews, collaborating with software engineers, QA and dev-ops. Focused on clinical trial software such as EDC or eCOA within a 21 CFR Part 11 regulated environment.

Wallace Hind Selection · Montpellier, France · £45,000 – £48,000 pa

Field-based role owning an established South West England and Wales territory for an international medical equipment manufacturer, selling into NHS and private hospitals across departments such as A&E, Renal, Oncology and Day Surgery. Involves rebuilding a neglected region, developing existing accounts and new business through complex multi-stakeholder procurement processes, with regular travel and trips to France for training and meetings.

Wallace Hind Selection · Cardiff · £45,000 – £48,000 pa

Field-based role selling a broad portfolio of medical equipment into NHS and private hospitals across South West England and Wales, covering departments such as A&E, Renal, Oncology and Day Surgery. You inherit an established customer base and live opportunities, with autonomy to build new business through complex multi-stakeholder procurement processes, reporting to the UK Managing Director.

Platform Recruitment · Cambridge · £35,000 – £45,000 pa

Develops FPGA and embedded firmware for high-performance data acquisition and signal processing systems used in biomedical research products. Writes VHDL for FPGA functionality and C for low-level hardware control, integrating and debugging digital electronics across the full product lifecycle alongside hardware and software engineers.

Gold Group · London · £40,000 – £55,000 pa

Plan and deliver human factors and usability activities across the full project lifecycle, from study design and fieldwork to analysis and reporting. Moderate research sessions and workshops internationally, applying methods such as contextual inquiry, usability validation and use-related risk analysis for medical devices and healthcare clients.

QIAGEN · Manchester

Lead the global Medical Affairs strategy for an oncology precision diagnostics portfolio, shaping biomarker and companion diagnostic initiatives with pharma and biotech partners across the drug development lifecycle. Engage key opinion leaders and cross-functional teams in a matrixed international environment, representing the company at conferences and advisory boards.

Sue Ross Recruitment Ltd · Sheffield · £32,000 pa

This role involves driving sales of medical devices through a consultative, virtual-first approach, combining clinical and technical expertise with strong account management. The candidate will identify customer needs, deliver product solutions, and develop strategic business plans to grow both existing and new accounts. Success requires analytical insight, proactive market awareness, and effective communication across video, phone, and in-person channels.

OrganOx · Oxford

Designs and develops electronic circuits and PCB layouts for medical devices, taking full lifecycle ownership from concept through to manufacturing handover. Work covers schematic capture, component selection, prototyping, debugging and verification against IEC 60601, collaborating closely with mechanical, software and systems engineers. Based on-site in Oxford with some remote design work.

Vero Hr · Cambridge · £45,000 – £55,000 pa

As a Quality & Regulatory Specialist, you will support clients in developing medical devices with a strong software focus, ensuring they meet regulatory requirements and quality standards. Your role involves creating and reviewing technical documentation, educating clients on regulatory needs, and collaborating with software engineers and senior stakeholders to deliver practical solutions.