Medical Technology Jobs

• Spring House, United States
• US$117,000 – US$201,250 pa
• Mid-level · manages people

Leads regulatory medical writing for the Immunology therapeutic area, preparing and finalizing clinical documents and serving as lead writer or point of contact for assigned programs. Manages direct reports, sets objectives, mentors junior writers and oversees external contractors, while driving process improvements and cross-functional coordination.

• London
• On-site
• £76,800 – £115,200 pa
• Senior

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.

ISO 13485 · ISO 14971 · IEC 62304 +3

• Milan, Italy
• Hybrid
• €31,200 – €46,800 pa
• Entry level

Acts as the primary point of contact for customers throughout the service and repair journey, managing requests, quotations, orders and escalations while coordinating with service engineers, repair centres and logistics teams. Supports quality and compliance in a regulated MedTech setting and contributes to process improvements, system enhancements and UAT activities.

Microsoft Office · Outlook · Excel +3

• Belgrade, Serbia
• Mid-level · manages people

Oversees local literature surveillance across 80+ territories, leading outsourced vendor operations and governance for global pharmacovigilance. Acts as business owner for controlled documents, policies and standards, driving standardisation and process improvement while partnering with cross-functional stakeholders across EMEA, Asia Pacific and other regions.

• Oxford
• On-site
• Mid-level
• Permanent

Assures software quality across the full lifecycle for medical devices up to IEC 62304 safety class C, covering design controls, requirements, verification and validation, and release management. A central duty is software risk management, developing and maintaining SFMEAs, hazard analyses and cybersecurity risk assessments aligned with ISO 14971. Works with R&D, Engineering, Post-Market Operations, Regulatory Affairs and Cybersecurity to support EU MDR and FDA compliance.

IEC 62304 · ISO 14971 · ISO 13485 +5

• Oxford
• On-site
• Lead
• Permanent

Technical lead for electronics design across current and next-generation medical device products, combining hands-on design with mentoring junior engineers. Defines electronic architecture, reviews schematics and PCB layouts, and oversees verification and validation including EMC and safety testing to IEC 60601, IEC 62304 and ISO 14971 standards. Works closely with suppliers, manufacturing partners, and cross-functional quality and regulatory teams on-site in Oxford.

IEC 60601 · IEC 62304 · ISO 14971

• Cambridge
• Lead · manages people
• Permanent

Leads complex medical-device and drug-delivery development programmes from concept through to manufacture, shaping technical strategy amid significant uncertainty. Manages multidisciplinary teams, guides clients through regulatory and commercial decisions, and mentors colleagues while building new business. Based at TTP's Melbourn campus near Cambridge.

• Bedford
• Hybrid · 3 days in office
• £50,000 – £60,000 pa
• Senior

Lead mechanical engineering across the full product lifecycle for fertility and pregnancy diagnostics, from concept and prototyping through to manufacture and launch. The role combines hands-on design in SolidWorks, DFM/DFA, FEA and tolerance analysis with process engineering, risk management (FMEA) and design transfer within a multidisciplinary R&D team, including work with suppliers in China.

SolidWorks · 3D CAD · IVDR +2

• Burgess Hill
• On-site
• £32,000 – £40,000 pa

Coordinating quality processes, managing non-conformances, supporting investigations and corrective actions, and maintaining ISO 9001 and ISO 13485 compliance. Reporting to the Head of Quality, the role covers document control, CAPA, supplier quality and audit support within a regulated packaging business, with scope to broaden experience across auditing and regulatory compliance.

Microsoft Office

• Newcastle-under-Lyme
• £50,000 – £60,000 pa
• Mid-level

Own and continually improve the Quality Management System in line with ISO 9001 and/or ISO 13485, maintaining documentation, procedures and records. Investigate complaints, supplier issues and non-conformances, lead root cause analysis and CAPA, and conduct internal audits supporting external certification. The role also involves hands-on support for purchasing, goods-in, stock control and warehouse operations.

ERP

• Cambridge
• Hybrid · 2 days in office
• £48,000 pa
• Permanent

Own data management across a portfolio of clinical studies, from setup through database lock and final data transfer, acting as the primary client contact for data quality and delivery. Configure and test data transfers, write production code, produce ETL-based reports, and maintain GCP documentation, with scope to improve SOPs and explore AI tools.

Python · SQL · SAS +2

• Henley-on-Thames
• £32,000 – £38,000 pa
• Mid-level
• Permanent

Support regulatory affairs and compliance across healthcare, digital health and medical-device activity. Maintain the Quality Management System, medical-device technical documentation, risk registers and audit actions, while coordinating evidence for tenders, CQC inspections and information governance. Acts as a link between clinical, technical and commercial teams.

ISO 13485 · ISO 14971 · IEC 62304 +7

• Aberystwyth
• On-site
• £39,000 – £45,000 pa
• Mid-level
• Permanent

Design and develop scientific monitoring instruments across the full product lifecycle, from schematic capture and PCB layout to prototyping, testing and production handover. Work within an R&D team on analogue and digital circuits, ARM microcontrollers, EMC compliance and automated test, supporting ISO 9001/14001 phase-gate processes.

Altium Designer · Oscilloscopes · Logic Analysers +7

• Greater Manchester
• Hybrid · 2–3 days in office
• £40,000 – £55,000 pa
• Mid-level
• Contract

Owns a diverse product portfolio in the Life Science/Healthcare sector, managing lifecycle activities from launches and range maintenance to discontinuations. Coordinates with supply chain, finance, regulatory and commercial teams on forecasting, availability and approval of product materials, while analysing market trends to inform decisions and reporting performance to senior stakeholders.

• Hatfield
• Lead · manages people

Lead a team of technicians in a repair centre, coordinating daily workloads while hands-on repairing and troubleshooting Patient Care Solutions and Ultrasound systems down to component level. Prepare quotations, manage parts and inventory, install and test hardware and software, and ensure ISO 9001 compliance and customer communication.

GE HealthCare Patient Care Solutions · GE HealthCare Ultrasound Systems · Servers +2