Latest Medical Device Software Engineer Jobs

Medical Field Service Engineer, CT & MRI Imaging

This role involves servicing, repairing, and maintaining advanced X-ray, CT, and MRI medical imaging systems at healthcare facilities across West London, Buckinghamshire, and Berkshire. You will receive comprehensive product training and work with cutting-edge technology, supported by a team of experienced engineers.

TRS Consulting Ealing, London, United Kingdom £45,000 – £50,000 pa

On-site Permanent

Medical Affairs Director | Johnson and Johnson| MedTech|UK

The Medical Affairs Director UK is a strategic leader responsible for shaping commercial strategy and driving innovation by leveraging deep surgical expertise and insights into the local healthcare ecosystem. Key responsibilities include stakeholder engagement, evidence strategy, and scientific leadership to support regulatory approval, market access, and clinical adoption of J&J MedTech products.

Johnson & Johnson MedTech Liverpool, United Kingdom

On-site Permanent

Medical Affairs Director | Johnson and Johnson| MedTech|UK

The Medical Affairs Director UK is a strategic leader responsible for shaping commercial strategy and driving innovation by leveraging deep surgical expertise and insights into the local healthcare ecosystem. The role involves building strong stakeholder relationships, ensuring robust evidence for product approval and market access, and communicating scientific and clinical data effectively.

Johnson & Johnson MedTech Birmingham, United Kingdom

On-site Permanent

Regulatory Affairs Manager

Cure Talent are delighted to be partnered with a global medical device organisation recognised as one of the most established and successful healthcare companies in the world. With a diverse international footprint and a strong pipeline of innovation, the business...

Cure Talent Curbridge, Oxfordshire, United Kingdom

Territory Sales Manager

As a Territory Manager, you will drive sales growth for a premium portfolio of minimally invasive surgical devices and consumables across NHS and private hospitals. You will build strong relationships with surgeons, consultants, and theatre teams, support clinical cases, and manage existing accounts to maximize long-term revenue.

Progress Sales Recruitment Glasgow, City Of Glasgow, G2 1AL, United Kingdom £45,000 – £55,000 pa

On-site Permanent

Territory Sales Manager

As a Territory Manager, you will drive sales growth of surgical devices and consumables in NHS and private hospitals across the North East, Scotland, and North West England. You will build strong relationships with surgeons and clinical teams, support clinical cases, and manage both new and existing accounts to maximize long-term revenue.

Progress Sales Recruitment York, YO1 8RS, United Kingdom £45,000 – £55,000 pa

On-site Permanent

Process Project Engineer – Moulding / Manufacturing

Process Project Engineer – Moulding / ManufacturingRoleExciting new role with our client a multinational Medical Device and Healthcare products provider. NIRAS is actively recruiting for an energetic and hands-on Manufacturing/Project Engineer to lead a key project within our Client’s Advanced...

NIRAS Ireland Castlebar, Mayo County, Ireland

Quality Engineer

The Quality Engineer will manage and coordinate customer complaints for medical instruments and orthopaedic products, conduct internal audits, and maintain quality procedures. The role involves working independently, leading meetings, and ensuring regulatory compliance in a growing SME.

E-Personnel Recruitment Guildford, Surrey, United Kingdom £45,000 – £50,000 pa

Hybrid Permanent

Quality Engineer (Compliance)

This role involves ensuring medical device and drug-device combination products meet strict regulatory and quality standards throughout development. The Quality Engineer will lead design controls and risk management activities, support audits, and ensure compliance with ISO and FDA regulations. They will work closely with development teams and external partners to maintain audit-ready documentation and contribute to regulatory submissions.

Next Phase Recruitment Cambridge, Cambridgeshire, United Kingdom

Hybrid Contract

Assembly Technician

Client;We are proud to be working alongside a truly ground-breaking medical device business, who are looking to appoint a process/assembly technician.POSITION; Process/Assembly TechnicianSHIFT; Monday - Friday 8 - 4:30Hourly Rate - £14.00 - £14.25 an hour.The key responsibilities for this...

Planet Recruitment Oxford, Oxfordshire, United Kingdom £14 – £14 ph

Technical Documentation and Development Engineer

A Technical Documentation & Development Engineer is required to support medical device product development through robust documentation, CAD formalisation, and regulatory compliance. The role focuses on ensuring all new and legacy products meet MDR requirements, with a strong emphasis on...

Michael Page Sheffield, South Yorkshire, United Kingdom

Business Development Manager PRS South East

This role involves driving business growth for a leading provider of biologics and medical devices within the South East of England. The Business Development Manager will develop new accounts and expand existing relationships across NHS and private healthcare institutions, focusing on surgical specialities such as ENT, Breast Reconstruction, Maxillofacial, Ophthalmology, and General Surgery. The role requires consultative selling, product demonstrations, and close collaboration with clinical teams to support patient outcomes.

Force Recruitment South East England, United Kingdom £45,000 – £60,000 pa

Hybrid Permanent

Regulatory Affairs Specialist

As a Regulatory Affairs Specialist, you will work within a global team to ensure medical devices meet regulatory requirements. Your responsibilities include preparing regulatory submissions, collaborating with project teams, and maintaining compliance throughout the product lifecycle.

Smith & Nephew Watford, United Kingdom

Hybrid Permanent

Regulatory Affairs Specialist

As a Regulatory Affairs Specialist, you will work across regions and products, preparing global regulatory submissions and maintaining compliance for Smith & Nephew's orthopaedic portfolio. You will collaborate with project teams to develop regulatory strategies, support product changes, and ensure adherence to international regulations.

Smith & Nephew United Kingdom

Hybrid Permanent

Production Scheduler

The Production Scheduler will plan, coordinate, and monitor production activities across multiple projects in a regulated medical device manufacturing environment. Key responsibilities include developing realistic schedules, working closely with cross-functional teams, and supporting continuous improvement initiatives.

Euro Projects Recruitment Abingdon, Oxfordshire, OX14 5BH, United Kingdom £40,000 – £45,000 pa

On-site Permanent