Medical Technology Jobs

• 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

• 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

• Coventry

Owns territory business plans and sales targets for electrophysiology products across West Midlands hospital accounts, driving catheter utilisation and capital sales to grow market share. Builds clinical and non-clinical customer relationships, manages tenders and local pricing, and executes EMEA marketing launches alongside regional sales and technical specialist colleagues.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint +1

• Allschwil, Switzerland
• Mid-level

Lead Pharmacovigilance process and training projects, including process development, mapping, and training qualification and delivery, while acting as a quality partner for the Office of the Chief Medical Officer. Drive digital transformation toward data-centric content and a robust qualification management system, managing timelines, risks, and audits across a matrixed organization.

• Cambridge
• Mid-level

Provide regulatory support across a Cambridge product development business, guiding multidisciplinary engineering and science teams on compliance with ISO 9001, ISO 13485 and FDA 21 CFR 820. Monitor international regulatory changes, support external audits and contribute to quality management system improvements across medical and non-medical projects.

• Cambridge
• On-site
• Senior

Design and develop complex medical devices as part of a multidisciplinary team of mechanical engineers, physicists and electronics engineers. The role is hands-on, spanning CAD, prototyping and functional mechanism design across multiple medical specialisms, including some surgical robotics, with variety rather than a single-device focus.

CAD

• Cambridge
• £80,000 – £100,000 pa
• Lead · manages people

Lead electronics design and development for a Cambridge R&D company building state-of-the-art medical devices. You'll act as technical figurehead, running a small team, overseeing product development from concept to manufacture, and liaising with customers and senior stakeholders. Requires strong analogue/digital design, embedded C/C++, and prior technical lead or mentoring experience.

• Leicester
• £35 – £40 ph
• Senior

Owns mechanical design projects for bespoke automation and robotic systems, from concept through build, installation and customer handover. Produces 3D CAD models, drawings and BOMs, leads design reviews, and works with electrical engineers, fitters and customers. Requires strong Solid Edge or similar CAD skills and UK travel.

Solid Edge · SolidWorks · Inventor +1

• Cambridge
• On-site
• £40,000 – £50,000 pa
• Mid-level

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.

Altium

• Leicester
• £40,000 – £50,000 pa
• Mid-level

Designs electrical control and safety systems for bespoke automated machinery, producing EPLAN schematics, control panel designs and bills of materials, and ensuring CE compliance. The role spans the full project lifecycle, from risk assessments and panel build supervision to commissioning, fault-finding and customer technical support, working with PLCs and industrial robots.

EPLAN · PLC · Omron +7

• London
• £300 – £312 pd
• Senior
• Contract

Senior product design engineer role at a consultancy, working across medical, consumer and industrial products. You'll translate client briefs into technical requirements, build SolidWorks CAD models, run feasibility and risk analysis, specify materials and manufacturing methods, and lead projects from ideation through to production-ready manufacture. Involves prototyping, testing and presenting to clients alongside industrial designers and human factors specialists.

SolidWorks · Adobe Illustrator · Arduino +1

• Burgess Hill
• Hybrid
• £49 – £86 ph
• Lead
• Contract

Leads the authoring, review and lifecycle management of clinical and performance evaluation documentation for a global diagnostics organisation, including protocols, study reports, investigator brochures and regulatory submissions. Works cross-functionally with regulatory, quality, R&D and medical affairs teams, conducting literature reviews and synthesising complex data under IVDR and GCP. Initial 12-month contract, hybrid with up to three days on site.

AI-enabled tools

• Cardiff
• £40,000 – £50,000 pa
• Mid-level

Owns process performance in a regulated medical device manufacturing environment, driving OEE, yield and flow improvements through Lean and structured problem-solving. Works hands-on on the shop floor with operators and maintenance on fault-finding, machine trials, process validation and documentation such as PFMEAs and process maps. Covers double day shifts with an on-call weekend rotation.

Microsoft Excel · 2D CAD · 3D CAD +2

• Surrey
• Hybrid
• £200 – £300 pd
• Mid-level
• Contract

Supports a global pharmaceutical organisation's digital health strategy by identifying and evaluating early-stage opportunities that combine digital technology with healthcare products. Day to day involves market research, business case and value proposition development, external partner assessment, and Agile activities such as sprint planning and OKR reviews, working with commercial, medical, technology and brand teams.

• 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