93 jobs
Johnson & Johnson MedTech Beerse, Belgium €79,800 – €137,770 pa
Oversees the end-to-end process for internal and external clinical data sharing requests, ensuring compliance with privacy standards and procedures. Manages vendors handling anonymisation and synthetisation, and acts as the primary contact for YODA Project requests, securing clinical team approvals. Supports external research teams using clinical study data.
Johnson & Johnson MedTech Birmingham
Field-based role covering hospital accounts across the West Midlands, building territory plans and driving catheter utilisation and capital sales in electrophysiology. Involves developing clinical and non-clinical customer relationships, executing EMEA marketing strategies, managing tenders and local pricing, and working alongside sales specialists and technical teams.
Smith & Nephew UK - Field
Field-based sales role covering South Wales, Cheltenham, Gloucester and Worcestershire, owning strategic accounts and driving revenue growth for Sports Medicine focus brands. Involves quarterly business reviews, tailored proposals, CRM data analysis and engagement with senior clinical and NHS procurement stakeholders.
Smith & Nephew Stoke-on-Trent
Field-based clinical specialist role covering North Wales and the Midlands, acting as the go-to expert for complex wound care within the Advanced Wound Management portfolio. Combines hands-on clinical support, education of community healthcare professionals, relationship building and territory management to drive adoption of therapies such as NPWT.
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.
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.
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.
SoCode Cambridge £400 – £500 pd
Hands-on contract role running usability studies for advanced medical devices, covering the full study cycle from planning and moderating or observing sessions to analysing data and writing regulation-ready reports. The first project is a formative field study on cleaning and reprocessing workflows with real users, working alongside an established in-house human factors team following FDA-aligned quality procedures.
Morgan McKinley Bampton CA$40,000 – CA$50,000 pa
Hands-on role bridging R&D and production for next-generation fluidic products, building, wiring and commissioning assembly fixtures, automated test equipment and robotic cells. Involves process scale-up (precision dispensing, laser welding, leak testing), equipment validation (FAT/SAT, IQ/OQ/PQ) and continuous improvement using root-cause analysis and SPC. Works alongside senior engineers in a fully on-site manufacturing environment.
Reed Southampton £28,000 – £35,000 pa
Hands-on warehouse role combining physical duties with stock control and systems work for a medical device manufacturer. You will manage inventory accuracy, goods receipt, picking and dispatch, and help develop SAP and WMS processes alongside the Operations Director. Distinct for its blend of floor work and administrative process improvement.
Spectrum IT Recruitment Southampton £50,000 – £60,000 pa
Hands-on role combining project delivery, commercial and financial oversight, people management and quality/regulatory compliance within a small medical-sector business. You will lead business projects, manage resources and risks, support strategic planning, monitor budgets and expenditure, and maintain compliance with medical device regulations while building customer, supplier and partner relationships.
HAYS Specialist Recruitment Oxford
Provide quality oversight across clinical activities and the Quality Management System, leading internal, external and vendor audits, managing quality events, CAPAs and root cause investigations, and supporting regulatory inspection readiness. Work cross-functionally with Clinical Operations, Pharmacovigilance, Regulatory Affairs and Quality to drive compliance across GCP, GCLP and GVP activities.
