28 jobs
Bluetree Cambridge £65,000 – £80,000 pa
Lead regulatory strategy for a cardiology device company expanding into the US, UK, EU and Middle East, owning FDA, CE and UKCA submissions from Class I to Class II/III. Drive an audit-ready QMS (ISO 13485, 21 CFR Part 820, ISO 14971) and advise senior leadership on regulation, quality and clinical governance, working directly with the FDA, MHRA and notified bodies.
Ernest Gordon Recruitment Mitcham £40,000 – £45,000 pa
Field-based role servicing biomedical and aesthetic laser equipment across a London patch, with occasional UK travel and roughly two nights away per month. The engineer receives manufacturer-funded training and certification on high-complexity medical lasers, with a progression plan toward senior positions. Working Monday to Friday, 40 hours per week, with time off in lieu for excess hours.
Impact Recruitment Aldershot £45,000 – £55,000 pa
Hands-on mechanical design role taking safety-critical respiratory protective equipment from concept through 3D CAD modelling, prototyping, testing and production. Involves detailed drawings, DFMEA, jig and fixture design, NPI and technical support, working closely with manufacturing, quality, customers, suppliers and external test organisations.
Matchtech Fareham
Maintains and improves a medical device Quality Management System, planning and reporting internal audits and leading external audit readiness with evidence packs and follow-up actions. Supports ISO 13485 compliance, ISO 14971 risk activities, CAPA and document control, and leads quality improvement projects in a regulated scale-up environment.
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.
Smith & Nephew UK - Field
Designs and delivers medical education programmes on Advanced Wound Management across the Nordics, UK & Ireland and Canada, working with healthcare professionals, clinical experts and professional societies. Blends in-person and digital learning, manages programme logistics and outcomes, and collaborates with Medical Education, Marketing, Professional Affairs and Commercial teams. Field-based with extensive travel (up to 70%).
Johnson & Johnson MedTech Brussels, Brussels-Capital Region, Belgium
Supports intraocular lens proctoring and medical information requests, analysing surgical cases and post-operative outcomes to optimise clinical results. Provides clinical guidance to healthcare professionals, tracks MIR statistics, and collaborates with Product Safety, Marketing and R&D on new product introductions. Home-office based with up to 20% travel across EMEA.
Newton Colmore Cambridge
Provide regulatory support across a product development organisation, working with engineers and scientists to align projects with global requirements. Maintain and improve the QMS, apply ISO 9001, ISO 13485 and FDA 21 CFR 820, monitor regulatory changes, and support external audits.
Healthium Clinics Henley-on-Thames £35,000 pa
Supports market access, quality systems and governance across healthcare and technology activity, coordinating evidence packs, tenders and regulatory documentation. Maintains the Quality Management System, risk registers and audit actions, and monitors MHRA, CQC, NICE and ICO requirements. Works with clinical, technical and commercial colleagues to keep registrations and controls inspection-ready.
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.
HCRG Care Group Runcorn £50,000 pa
Leads end-to-end data migration projects moving sensitive patient records between Electronic Patient Record systems, coordinating internal teams, external organisations and suppliers. Combines technical project management with data quality, information governance and clinical safety, working closely with the Head of Clinical Systems. Predominantly remote with occasional UK travel.
Evolve Selection Leeds
Owns a spinal and cranial technology portfolio across the UK and Ireland, shaping commercial strategy, go-to-market plans and market access/reimbursement approaches. Works with sales, marketing, clinical experts and KOLs to drive adoption of robotics and next-generation solutions, with occasional travel to Belgium and the Netherlands.
Johnson & Johnson MedTech Pratica di Mare, Italy
Supports intraocular lens proctoring and medical information requests to ensure optimal clinical outcomes, analysing sub-optimal results and clinic workflow factors. Manages MIR responses within four days, generates statistics reports, and assists healthcare professionals with post-operative outcome analysis. Home-office based with up to 20% travel, reporting to the Associate Director of Clinical Services.
Johnson & Johnson MedTech IE009 Janssen Cilag Ltd
Supports intraocular lens proctoring and medical information requests to ensure optimal clinical outcomes, analysing sub-optimal results and clinic workflow factors. Manages MIR responses within four days, generates statistics reports, and assists HCPs with post-operative outcome analysis. Provides clinical expert support for new product introductions, demos and clinical studies, working home-office based with up to 20% travel.
