220 jobs
Johnson & Johnson MedTech Beerse, Belgium
Supports Clinical Risk Management operational excellence by coordinating process optimisation and day-to-day administration of the CRM digital landscape. Acts as operational point of contact for super-user forums, vendor coordination, taxonomy and metadata stewardship, portal support and audit or inspection evidence. Identifies and implements approved improvements while strategic ownership stays with CRM leadership.
Johnson & Johnson MedTech Issy-les-Moulineaux, France
Supports Clinical Risk Management operational excellence by coordinating process optimisation and the day-to-day administration of the CRM digital landscape. Acts as operational point of contact for super-user forums, vendor coordination, digital asset administration, taxonomy and metadata stewardship, portal support and audit or inspection evidence. Identifies and implements approved improvements while strategic ownership stays with CRM leadership.
Smith & Nephew Derby
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.
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 Milan, Italy
Leads commercial growth and adoption of connected care and digital health solutions across Western European hospital systems, negotiating multi-year enterprise agreements and guiding product launches. Manages a growing team and works with clinical, IT and executive stakeholders on interoperability and data integration. Remote with around 70% regional travel.
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.
Ernest Gordon Recruitment Mitcham £40,000 – £45,000 pa
Field-based role servicing biomedical devices across a London patch, with occasional UK travel and 2-3 overnight stays per month. The technician receives manufacturer-funded training to become certified on high-complexity medical lasers, with progression into more senior positions and time off in lieu for excess hours.
GE HealthCare United Kingdom, YY9 9YY
Provides day-to-day medical oversight for one or more clinical trials, ensuring patient safety, data integrity and protocol compliance. Reviews and assesses AEs and SAEs, supports safety signal detection with Pharmacovigilance, and advises investigators on eligibility and dosing. Works cross-functionally with Clinical Operations, Data Management, Biostatistics and Regulatory Affairs, and contributes to CSRs and regulatory submissions.
Theo James Recruitment Stockton-on-Tees £40,000 – £46,000 pa
Deliver NPI and engineering projects in a regulated medical manufacturing environment, focusing on process validation, PPAP documentation and quality compliance. Support projects from RFQ and feasibility through validation, customer approval and handover to production, working closely with Engineering, Quality, Operations and customers.
Yolk Recruitment Bridgwater £55,000 pa
Owns quality operations across a precision manufacturing site, maintaining QMS, certifications and audit readiness while leading continuous improvement. Acts as main contact for customers, auditors and suppliers, managing non-conformances, root cause investigations and corrective actions using SPC, PFMEA, PPAP and 8D. Also supports day-to-day Health & Safety activities alongside Production and Engineering teams.
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.
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.
Nexus Life Sciences Belfast £50,000 – £60,000 pa
Lead the Clinical Method Development and Validation team, overseeing bioanalytical method delivery for a New Product Development programme. The role combines hands-on expertise in extraction techniques and HPLC/UPLC/LCMSMS optimisation with managing and mentoring a team in a GLP-compliant environment, including regulatory submissions and audits.
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.
