Latest Medical Imaging Jobs

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

Product Specialist - Homecare Infusion

This role involves driving the adoption of premium infusion therapy devices in both hospital and homecare settings. The specialist will engage clinical stakeholders to influence decision-making and collaborate with homecare providers to ensure smooth patient therapy delivery. It's a field-based position combining clinical expertise with commercial sales, focused on parenteral nutrition, immunoglobulin, and home IV antibiotic therapies.

Progress Sales Recruitment London, United Kingdom £45,000 – £55,000 pa

Hybrid Permanent

Regulatory Affairs Specialist

The Regulatory Affairs Specialist will support the Quality & Regulatory team in maintaining and executing regulatory activities across a diverse product portfolio. Responsibilities include preparing technical documentation, ensuring compliance with global regulatory requirements, and coordinating audits. The role offers hands-on experience across the full product lifecycle and involves close collaboration with internal teams.

Cure Talent Uxbridge South, London, United Kingdom £40,000 – £50,000 pa

On-site Permanent

Senior Software Engineer

This role involves developing the software ecosystem for a next-generation wearable medical device, focusing on SDKs, desktop applications, and third-party integrations. You will work closely with firmware, hardware, and data science teams to ensure robust, compliant software solutions for clinical studies and commercial deployment.

Cure Talent Hathern, Leicestershire, LE12 5LA, United Kingdom £60,000 – £80,000 pa

On-site Permanent

Test Engineer

This role involves designing and implementing quality test procedures for both software and hardware components of medical devices. Responsibilities include attending design meetings, writing test plans, analyzing opportunities for automated testing, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa

On-site Permanent

Regulatory Manager

As a Regulatory Manager, you will lead regulatory strategy for drug-device combination products, working closely with global regulatory bodies and clients. You will manage a small team, contribute to regulatory intelligence, and represent the regulatory function in senior meetings.

HAYS Specialist Recruitment Cheshire, United Kingdom

On-site Permanent

Head of Product Development & Engineering

This role involves leading the product development lifecycle for complex medical technology products, from concept to launch and ongoing support. Responsibilities include managing R&D projects, providing strategic direction, mentoring a specialist team, and collaborating with various departments to ensure product success and regulatory compliance.

Concept Technical Worthing, West Sussex, United Kingdom £70,000 – £80,000 pa

On-site Permanent

Vulnerability Analyst

This role involves assessing known software vulnerabilities in Windows-based applications used in regulated medical devices. Responsibilities include performing exploitability and risk analysis, evaluating third-party component risks, and producing clear security documentation. The position requires 2+ years of commercial experience in application security and a strong understanding of CVEs and secure software concepts.

Real Limerick, Limerick County, Ireland £47 ph

Hybrid Contract

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

Regulatory Manager

As a Regulatory Manager, you will lead regulatory strategy for drug-device combination products, guiding clients through EU and US approvals. You will manage a small team, review key documentation, and represent the company in senior-level meetings.

Hays Life Sciences Cheshire, United Kingdom

On-site Permanent

Quality Assurance & Regulatory Affairs Specialist - MedTech

This role involves ensuring quality assurance and regulatory compliance across the full lifecycle of advanced medical devices, from design through manufacturing, for global markets including Europe, North America, and APAC. The specialist will conduct internal audits, help shape regulatory strategy, and work with complex, innovative technologies in a high-autonomy environment. The role focuses on new product development, requiring strict adherence to ISO 13485, CE Marking, and other international standards.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom £45,000 – £49,000 pa

On-site Permanent

Regulatory Affairs Specialist

This role involves preparing and managing regulatory submissions for medical devices, ensuring compliance with EU MDR, ISO 13485, and global standards. The specialist will maintain technical documentation, support clinical evaluations, and collaborate with cross-functional teams throughout the product lifecycle, playing a key part in product registrations and post-market surveillance.

SRG Perivale, London, UB6 8DD, United Kingdom £50,000 – £60,000 pa

On-site Permanent

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

Test Quality Assurance Engineer

This role involves designing and implementing quality test procedures for both software and hardware in medical device products. Responsibilities include attending design meetings, writing test plans, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa

On-site Permanent