60 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.
Johnson & Johnson MedTech Beerse, Belgium
Senior analyst role accountable for global PLAN business process validation and release adoption across Transcend EMEA-OTC releases, working with the project team and local business partners to ensure successful release cut-over. Drives process scoping, testing strategy (BST, UAT, regression), solution design workshops, and operational readiness including SOPs and user access management. Serves as the business process single point of contact for PLAN stakeholders through hypercare and post-go-live stabilization.
Johnson & Johnson MedTech Madrid, Spain
Senior analyst role accountable for global PLAN business process validation and release adoption across Transcend EMEA-OTC releases, working with the project team and local business partners on release cut-over. Drives process scoping, testing strategy (BST, UAT, regression), solution design workshops, operational readiness, and hypercare for a multi-year SAP S/4HANA supply chain transformation.
Medtronic Watford £52,000 – £78,000 pa
Field-based clinical and technical expert supporting electrophysiology procedures and adoption of the Cardiac Ablation Solutions portfolio across London and Ireland. Provides on-site case coverage, 3D mapping system expertise, and training to physicians and hospital staff, collaborating with sales and clinical teams to drive safe technology use.
NHS Professionals Cambridge £20 – £24 ph
Undertake routine and specialist microbiological and molecular investigations across bacteriology, containment level 3, serology, chlamydia and molecular diagnostics, interpreting and reporting results. Operate and maintain automated analysers, manage consumables and use laboratory IT systems while supporting quality management, audits and SOP development. Based at Addenbrooke's Hospital within UKHSA's public health microbiology team.
ECM Selection Cambridge £45,000 – £55,000 pa
Develop embedded C and C++ software for medical devices spanning lab and hospital equipment, drug delivery systems and personal sensors. Work across all project stages from concept through design, implementation and manufacture, with substantial client interaction. Target systems include bare metal, RTOS and Linux, with Python used for automated testing.
NHS Professionals Worcestershire £20 pa
Perform biochemical analyses on patient samples using manual and automated techniques, maintain and QC point-of-care testing equipment, and authorise results for electronic reporting to wards. The role includes out-of-hours rota cover, giving technical advice to clinical staff, and supporting quality management within a hospital Clinical Biochemistry service.
Smith & Nephew Hull
Front-line quality role supporting a manufacturing value stream, reviewing and releasing product documentation, generating CoAs/CoCs, and performing raw material inspection. Leads containment, investigation and disposition of non-conforming materials, manages NCs and CAPAs, and acts as an SME during audits.
OrganOx Oxford
Accountable for end-to-end delivery of strategic New Product Development programmes, leading multidisciplinary teams across R&D, regulatory, quality, operations and commercial functions. Drives integrated programme plans, stage-gate governance, risk management, resource planning and budget forecasting for complex medical device development in a regulated environment, supporting the metra® organ perfusion platform.
OrganOx Oxford
Hands-on senior role designing, securing and automating Azure cloud infrastructure and CI/CD foundations for regulated medical device software and connected device services. Acts as a bridge between Digital and Data teams, supporting Databricks, SAP interfaces and enterprise data flows, with monitoring, observability and cybersecurity responsibilities. Office-based in Oxford with flexibility.
FIELD Brecon £33,000 – £38,000 pa
This role involves hands-on troubleshooting, maintenance, calibration, and repair of medical equipment both onsite and remotely within a leading hospital environment. The engineer will perform preventative maintenance, equipment upgrades, and ensure compliance with manufacturer guidelines and contractual KPIs. The position supports critical healthcare operations by maintaining the reliability and safety of advanced medical devices.
Medtronic London £76,800 – £115,200 pa
Supports software quality across the full product development lifecycle in Medtronic's surgical operating unit, from requirements and design through verification, validation, release and post-market support. Involves risk management (SFMEA, hazard analysis), design reviews, traceability documentation, CAPA and audit readiness, working closely with software, systems, regulatory and quality teams.
University of Leeds Leeds £41,064 – £48,822 pa
Develop a clinically deployable assay for therapeutic drug monitoring of the immunosuppressant tacrolimus, building on a recently created rapid, accurate and low-cost measurement method. Work within a multidisciplinary team focused on in vitro diagnostics assays and devices that improve dosing and patient outcomes, replacing slow mass spectroscopy workflows.
Newton Colmore Cambridge
Design and develop complex medical devices as part of a multidisciplinary team of mechanical engineers, physicists and electronics engineers. The role is hands-on, spanning CAD, prototyping and functional mechanism design across multiple medical specialisms, including some surgical robotics, with variety rather than a single-device focus.
Pertemps Gloucester Cheltenham £25,000 – £27,000 pa
Assembling precision medical devices within a controlled cleanroom, working to GMP standards and ISO procedures to meet production targets. The role involves handling small components with high accuracy in a fast-paced, high-volume environment, with full training provided. It offers a four-day week, Monday to Thursday, with Fridays off.
Omega Resource Group Gloucester £45,000 – £50,000 pa
Support and maintain the effectiveness of a medical device manufacturer's QMS in line with ISO 13485, MDR and FDA requirements. Day-to-day work covers CAPA effectiveness, quality data and trend analysis, non-conformances, change control and complaint investigation, plus writing and updating procedures and work instructions.
