Medical Technology Jobs

Johnson & Johnson MedTech · Titusville, United States · US$112,000 – US$180,550 pa

Operational leader supporting the Immunology regulatory portfolio, translating global regulatory strategy into executable plans and coordinating cross-functional teams. Facilitates Global Regulatory Team meetings, manages health authority meeting planning and worldwide submissions, and leads change management for new processes and system rollouts across the RPM department.

Johnson & Johnson MedTech · Cambridge, United States · US$112,000 – US$180,550 pa

Operational leader supporting the Immunology regulatory portfolio, translating global regulatory strategy into executable plans and coordinating cross-functional teams. Facilitates Global Regulatory Team meetings, manages health authority meeting planning and worldwide submissions, and leads change management for new processes and system rollouts. Works with tools like Planisware, Veeva and Microsoft Project.

Medtronic · Watford · £62,800 – £94,200 pa

Defines and executes pricing strategy across a product and service portfolio, analysing trends, running diagnostics and modelling opportunities in Excel. Partners with country, regional and global teams across Western Europe, Japan and Australia on tenders, deals and value-based healthcare programmes, driving pricing mindset change in a matrix organisation.

Medtronic · Paris, France · €70,400 – €105,600 pa

Drives pricing strategy across a medical technology product portfolio, evaluating pricing trends, building stakeholder consensus and reviewing tenders and deals against revenue and profit targets. Works cross-functionally with Western Europe, Japan, Australia/New Zealand and global operating units to embed pricing as a strategic profit lever and implement value-based business models.

SoCode · Cambridge · £400 – £500 pd

Hands-on contract role running usability studies for advanced medical devices, covering the full study cycle from planning and moderating or observing sessions to analysing data and writing regulation-ready reports. The first project is a formative field study on cleaning and reprocessing workflows with real users, working alongside an established in-house human factors team following FDA-aligned quality procedures.

SoCode · Cambridge · £40,000 – £50,000 pa

Hands-on electronics design role at a product development consultancy, owning hardware at system and circuit level from concept through prototyping, debug, verification and into production for medical and healthcare clients. Work spans medium and high-volume manufacture in well-equipped labs, with peer review across disciplines and a new technical challenge every few months.

Vertech Group (UK) Ltd · London · £75,000 – £85,000 pa

Assesses software development processes and technical evidence for AI-enabled medical devices, reviewing lifecycle, V&V, configuration management and risk to determine whether safety-critical products meet certification standards. Uses AI-assisted tools to explore evidence, identify failure modes and flag inconsistencies within a specialist team.

SRG · Great Yarmouth · £30,000 – £37,700 pa

Working within a QA team at a GMP manufacturing site producing pharmaceuticals, medical devices and personal care products, you will monitor and assure the quality of processes and products. Duties include preparing and approving quality documentation, investigating GMP breaches and OOS incidents, managing CAPAs, supporting site audits and QP batch release, and delivering GMP training.

Appcast Enterprise · South Yorkshire

Operates and performs basic setups on CNC 2 and 3 axis lathes, EDM wire and plunge machines, running multiple machines simultaneously to produce medical device components. Also uses manual machine tools to cut, drill, shape and finish parts, completing shop work orders, inspection documentation and daily maintenance sheets while following QMS procedures and safety standards.

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.

Automation Experts Ltd · Leicester · £40,000 – £50,000 pa

Electrical Design Engineer£40-50k + Competitive Salary, Bonus, Employee Ownership BenefitsLeicestershire. Ref: 25464Would you like to design and deliver cutting-edge automation and robotic systems for world-class manufacturing customers?This is an exciting opportunity to join a highly successful automation engineering business that...

Smith & Nephew · Watford

Owns the global OT cybersecurity programme across a medical technology manufacturer's worldwide manufacturing network, setting governance and embedding security into how industrial technologies are designed and operated. Leads risk management, incident response and secure modernisation aligned to IEC 62443 and NIST frameworks, influencing engineering, IT and business stakeholders without direct control of implementation teams.

Newton Colmore · Cambridge

Lead the design and development of next-generation drug delivery devices, guiding multidisciplinary teams of engineers, scientists and designers from early-stage concepts through to manufacturable solutions. The role blends hands-on R&D work — concept generation, prototyping, verification planning and risk management — with programme leadership and client-facing consultancy, advising stakeholders on technical decisions and development pathways.

Pertemps Leeds · Uttoxeter · £31,000 – £34,000 pa

Manufacture high-accuracy calibration gases and reference materials using gravimetric methods, producing oxygen and flammable gas mixtures to strict ISO 6142 and ISO 17034 standards. Duties include preparing cylinders, valve fitting, stock control and site logistics, working within a specialist production team for a global industrial and medical gases leader.

Carbon 60 · London · £50 – £65 ph

Analyses post-market complaints and quality data for a global medical device portfolio, leading monthly product quality monitoring and statistical trending to surface emerging risks. Builds and maintains Power BI dashboards and reporting tools, conducts complaint investigations and ad hoc reviews, and supports EU MDR trending, audits and CAPA activities alongside Quality, Regulatory, Clinical, R&D and Operations teams.