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 · Blackpool

Accountable technology leader for the DePuy Synthes EMEA Deliver domain, owning the regional logistics technology roadmap across ERP, WMS, WCS/WES, TMS, warehouse automation and partner integrations. Balances multi-year transformation delivery with operational reliability, cybersecurity, compliance and lifecycle governance, while leading a team and governing 3PL and vendor technology relationships.

Smith & Nephew · UK - Field

Field-based sales role covering the London territory, promoting a medical technology portfolio to NHS and private customers. You build relationships, follow up leads, provide product training and technical advice, and track competitor activity and market trends. Suits a new graduate or someone with clinical skills moving into a commercial career.

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.

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.

Newton Colmore · Cambridge

Consultative, relationship-led business development role focused on medical device innovation, working with clients on surgical technologies, wearables, implantables and diagnostics. Involves building a pipeline, shaping proposals, negotiating commercial agreements and supporting go-to-market strategy, while collaborating closely with scientists and engineers. Suits a technically credible candidate, ideally post-doc level, who can translate scientific depth into client conversations and partnerships.

Medtronic · Dublin, Ireland

Leads the EMEA Service Marketing strategy for a global healthcare technology company, working across operating units and regional teams to develop service offerings and drive commercial growth. Combines strategic marketing, commercial planning, sales enablement and customer engagement, using market insights and competitive analysis to expand market share. Involves travel within the EMEA region.

Newton Colmore · Cambridge

Design and develop novel mechatronic systems for medical devices, including liquid handling machines and surgical robotics, within a multidisciplinary R&D team. Take concepts through iterations to manufacture, designing intricate mechanisms while owning wider system development. Open on sector background, though medical or biotech experience is valued.

Clearline Recruitment Ltd · Welwyn Garden City · £38 – £56 ph

Independently manages end-to-end clinical data management across one or more studies, from CRF and database design through to final study closure. Works closely with Biostatistics, Data Science and Clinical Operations, overseeing data vendors and resolving complex issues across EDC, ePRO and IRT systems. Requires strong knowledge of CDISC standards and risk-based monitoring.

Reed Technology · Cambridge · £85,000 – £100,000 pa

Lead information security, product cybersecurity and cyber risk management for a digital health organisation, owning the ISMS, policies and controls. Day to day involves risk assessments, threat modelling, penetration testing oversight, cloud and application security, incident response and supporting audits and regulatory submissions. Works closely with software development, quality, regulatory and clinical teams, acting as the security subject matter expert.

ProTech Recruitment Ltd · Dorking · £45,000 – £55,000 pa

Owns product quality issues in a fast-paced manufacturing setting, leading root cause investigations and corrective actions using 8D, 5 Whys, Fishbone, FMEA and SPC. Partners with Engineering, Production and Supply Chain on continuous improvement, defect prevention, new product introduction and engineering change reviews, in a regulated ISO 13485/9001 environment.

Platform Recruitment · Cambridge · £60,000 – £65,000 pa

Hands-on role designing custom electronic circuit boards from customer requirements, covering schematic capture, PCB layout, board bring-up, verification and test. You'll liaise with clients on integration and commissioning, write technical reports, and work across IoT, medical device and robotics projects in a consultancy team.

GE HealthCare · United Kingdom, YY9 9YY

You will install, maintain and repair CT, PET and Nuclear Medicine systems across the Midlands and wider UK, diagnosing complex multi-technology faults and providing remote diagnostics from a home office. The role involves roughly 35-40% travel with occasional overnight stays, plus overtime, short-notice callouts and weekend shifts, working closely with healthcare professionals and engineering teams.

A259 Recruitment · Wick · £13 ph

Assemble small plastic components for medical and non-medical devices at a client site in Littlehampton, working on a production line with full training and uniform provided. Shifts cover day, twilight or night patterns across Monday to Friday, with the role starting as temporary and transitioning to permanent after 12 consecutive weeks.

Clearline Recruitment Ltd · Welwyn Garden City · £377 – £550 pd

Operational delivery of early-phase clinical trials, coordinating multi-country study activities, timelines and site start-up while managing vendors, CROs and study documentation such as Trial Master Files. Works closely with international study teams and cross-functional groups to ensure ICH-GCP compliance, manage risks and improve study processes.