Medical Technology Jobs

• Gloucester
• On-site
• £45,000 – £50,000 pa
• Mid-level
• Permanent

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.

ISO 13485 · FDA Quality System

• 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

• Lancashire
• On-site
• Mid-level
• Contract

Maintains and improves a medical device Quality Management System in line with ISO 13485 and FDA QSR, leading non-conformance, deviation, complaint and CAPA investigations with root cause analysis. Supports internal, supplier and regulatory audits, risk management under ISO 14971, validation and design transfer, working with Manufacturing, R&D, Regulatory Affairs and Supply Chain.

• Fareham
• Hybrid
• Mid-level
• Permanent

Maintains and improves a medical device Quality Management System, planning and reporting internal audits and leading external audit readiness with evidence packs and follow-up actions. Supports ISO 13485 compliance, ISO 14971 risk activities, CAPA and document control, and leads quality improvement projects in a regulated scale-up environment.

• Houghton le Spring
• On-site
• Temporary

Support quality assurance, product compliance and regulatory activities in a medical device manufacturing environment. Maintain quality control systems, prepare technical documentation, conduct testing and inspections, investigate non-conformances using CAPA, analyse quality data and support internal and external audits, working closely with the QA Manager and production teams.

ISO 13485 · EU MDR

• 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

• 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

• Gloucestershire
• £58,000 – £63,000 pa
• Senior

Owns packaging and labelling validation for a global medical device portfolio, leading transportation testing, shelf-life studies and equipment validation projects. Reviews technical documentation, BOMs and labelling content, leads CAPAs and non-conformance investigations, and acts as key contact during regulatory audits. Works cross-functionally with Quality, Regulatory, R&D and Manufacturing, mentoring junior staff.

ASTM

• Stockton-on-Tees
• £40,000 – £46,000 pa

Plans, coordinates and documents process validation activities across NPI and manufacturing projects, preparing protocols, reports and technical evidence. Works with Engineering, Quality, Operations and customers on PPAP submissions, FMEAs and process flow diagrams to demonstrate manufacturing readiness in a regulated medical manufacturing environment.

• Cambridge
• Hybrid
• £50,000 – £65,000 pa
• Senior · manages people

Hands-on role turning system and sub-system requirements into verification strategies, including test protocols, bespoke rigs and automated Python scripts, through to formal sign-off. Results feed back to design teams and regulatory submissions, and you'll lead and mentor a small group of verification engineers on a complex electromechanical medical device.

• London
• Hybrid · 3–4 days in office
• £76,800 – £115,200 pa
• Senior

Designs and builds automated test frameworks for embedded and connected hardware used in operating rooms, covering device software, firmware integrations and hardware-software interaction rather than web or mobile apps. Works with Android AOSP, Linux edge devices and IoT gateways, validating drivers, connectivity, OTA updates and service APIs, and embedding quality gates into CI/CD pipelines alongside hardware, firmware and systems engineers.

Android · Linux · Jenkins +7

• Houghton le Spring
• £37,000 – £40,000 pa
• Contract

Support quality and regulatory requirements across design, manufacture and testing of medical devices. Maintain quality procedures, analyse performance data, manage CAPA activities, and assist with inspections, audits and clean-room production standards. A 12-14 month maternity cover contract within a specialist manufacturing environment.

• Cardiff
• On-site
• £50,000 pa
• Mid-level
• Shift work

Owns a highly automated production line at a global medical device manufacturer, combining hands-on fault-finding, root cause investigation and continuous improvement to raise machinery reliability and cut downtime. Works on a two-shift rotation with weekend on-call, partnering with production, maintenance and quality teams on OEE, process validation and NPI.

Power BI · PLC · HMI +2

• Oxford
• On-site
• Senior · manages people
• Permanent

Leads a team of Windows software engineers building device-hosted applications and services for Class II and III medical devices, covering GUI development, connectivity and cybersecurity mitigations. Owns the full SDLC, regulatory compliance (FDA, ISO 13485, IEC 62304), roadmaps, budgets and hiring, while acting as technical representative to regulators, partners and customers.

Windows

• Houghton le Spring
• On-site
• Mid-level
• Temporary

Support the design, manufacture, testing and regulatory compliance of medical devices, maintaining quality control systems, production protocols and documentation. Investigate non-conformances and complaints, run CAPA, testing and validation, and assist with EU MDR, ISO 13485 and audit readiness, including clean room operations.