Medical Technology Jobs

• Warsaw, Poland
• Hybrid
• PLN 88,000 – PLN 132,000 pa
• Entry level

Primary point of contact for customers through 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

• Heerlen, Netherlands
• Hybrid
• €40,000 – €60,000 pa
• Entry level

Serve 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 centers and logistics teams. Support quality and compliance in a regulated MedTech setting and contribute to process improvements, system enhancements and UAT activities.

Microsoft Office · Outlook · Excel +3

• Blackpool
• Mid-level

Owns and optimises assigned manufacturing value streams to ensure safe, compliant and cost-effective production of medical devices. Provides technical leadership, directs complex process development and validation programmes (IQ, OQ, PQ), leads continuous improvement initiatives and mentors junior engineers while representing Engineering in governance and regulatory forums.

Siemens · Rockwell · HMI +1

• Maidenhead
• Lead · manages people

Lead the governance, design and documentation of application integrations across the software development lifecycle, focusing on Supply Chain systems with hundreds of connected satellite systems. Own end-to-end integration design, coordinate estimates and delivery with vendor build teams, and support testing and cutover. Emphasis on SAP integration technologies, observability, and applying AI and intelligent automation to the SDLC.

SAP BTP IS · SAP PI/PO · SAP +7

• 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
• 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

• Witney

Joins the Operations Engineering team to introduce bespoke automated production machines and own their validation strategy, from project planning and risk assessment through to delivering validated equipment into Production. Develops new validation tests, executes process equipment validations, and becomes a technical subject matter expert working with cross-functional teams and suppliers, with occasional supplier site visits.

Automated Machinery · Machine Vision

• Dorking
• On-site
• Mid-level
• Permanent

Resolve customer-raised product quality issues, lead root cause analysis using 8D, 5 Whys and Fishbone, and drive permanent corrective actions within a Quality Management System. Support new product introductions, review engineering changes, and track KPIs like Defects Per Unit while working cross-functionally with Production, Engineering and Supply Chain in a manufacturing environment.

Excel · Pivot Tables · Pareto Charts

• Cambridge
• Permanent

Lead and contribute to technically ambitious surgical device projects, applying ultrasound expertise across the innovation lifecycle from early feasibility to product launch. Engage directly with clients to shape strategy and grow a presence in the surgical technology community, working on robotic-assisted surgery systems and intelligent instruments with embedded sensors.

60601-2-37

• Hertfordshire

Own product regulatory compliance end to end, acting as the company's official representative and evidencing compliance to external parties. Advise on sourcing, development, composition, packaging, labelling and marketing, horizon-scan regulatory changes, and support domestic and European product registrations plus safety data sheet software. Requires REACH/CLP knowledge and a chemical or QA background.

MS Office · Word · Outlook +2