Latest Regulatory Affairs Specialist Jobs

Clinical Development Specialist

This role involves leading the launch and adoption of the Affera Mapping System and Cardiac Ablation Solutions (CAS) portfolio. Responsibilities include site initiations, providing clinical and technical expertise, training clinicians, and ensuring regulatory compliance. The role requires a strong background in electrophysiology and ablation technologies, with a focus on 3D mapping systems and complex EP procedures.

Medtronic Watford, United Kingdom

On-site Permanent

Upstream Product Manager

The Upstream Product Manager will lead the strategy and early-stage development of AI-enabled and edge-based software solutions for the Touch Surgery ecosystem. Responsibilities include defining product vision, conducting market research, partnering with engineering teams, and developing go-to-market strategies. The role requires deep expertise in AI, edge computing, and software marketing.

Medtronic London, United Kingdom

On-site Permanent

Packaging Engineer

ABOUT ORGANOX:OrganOx is a commercial stage organ technology company dedicated to developing technologies to improve outcomes for patients with acute or chronic organ failure. The company was established as a spin out of the University of Oxford in 2008 and...

OrganOx Oxford, United Kingdom

On-site Permanent

Senior Electronics Design Engineer

ABOUT ORGANOX:OrganOx is a commercial stage organ technology company dedicated to developing technologies to improve outcomes for patients with acute or chronic organ failure. The company was established as a spin out of the University of Oxford in 2008 and...

OrganOx Oxford, United Kingdom

On-site Permanent

Marketing Manager (RENASYS)

Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.Are you driven by the opportunity to help shape global marketing strategy in a fast moving, innovation led environment? This is a chance to play a...

Smith & Nephew Watford, United Kingdom

Surgical Training Technician

As a Surgical Training Technician, you will prepare and maintain laboratory spaces for surgical education, support live training sessions, and ensure compliance with regulatory frameworks. You will work closely with Medical Education, Marketing, and R&D teams, managing stock levels and maintaining inventory systems.

Smith & Nephew Watford, United Kingdom

On-site Permanent

Senior Embedded Software Engineer - Medical Devices

This role involves designing, developing, and maintaining high-integrity embedded software for medical devices, ensuring compliance with ISO 13485 and other medical standards. The Senior Embedded Software Engineer will lead software architecture, design reviews, and technical decision-making, while collaborating with hardware, systems, and quality teams.

Verso Recruitment Milton, Cambridgeshire, Cambridgeshire, United Kingdom £60,000 – £70,000 pa

On-site Permanent

Senior Pharmacovigilance Scientist - Signal Management

The Senior Pharmacovigilance Scientist will lead safety signal management activities, write aggregate reports, and support clinical trial pharmacovigilance. They will also serve as a subject-matter expert on global safety regulations and ensure compliance with regulatory bodies.

Hays Life Sciences London, City And County Of the City Of London, United Kingdom £80 – £109 ph

Remote Contract

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

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

Production Scheduler

As a Production Scheduler, you will plan and coordinate production activities for multiple projects in a low-volume, R&D-focused medical device manufacturing environment. You will ensure efficient resource allocation, timely delivery, and compliance with ISO13485 standards, acting as a key liaison between manufacturing, supply chain, quality, and engineering teams.

Euro Projects Recruitment Shippon, Oxfordshire, United Kingdom £40,000 – £45,000 pa

On-site Permanent

Field Service Engineer - Medical diagnostic equipment

This role involves providing high-quality technical service and support for ophthalmic and medical diagnostic equipment across the UK and internationally. Responsibilities include installations, repairs, maintenance, and troubleshooting, as well as responding to breakdowns, maintaining service records, and ensuring compliance with regulatory standards.

Zest Business Group Berkshire, United Kingdom £35,000 – £45,000 pa

On-site Permanent

Senior Service Engineer

This role involves providing technical service, installation, and maintenance for advanced medical diagnostic equipment, including ophthalmic and imaging systems. You will troubleshoot hardware and software issues, maintain service records, and train clinical staff, with extensive travel and occasional weekend work required.

Alecto Recruitment Wokingham, Berkshire, United Kingdom £40,000 – £45,000 pa

Permanent Flexible

Mechanical Engineer

This role involves taking ownership of mechanical engineering aspects for key project subsystems and new technology developments. You will collaborate with multi-disciplinary teams, uphold best-practice design standards, and ensure compliance with international regulations in a high-tech manufacturing environment.

Randstad Engineering Bristol, Bristol (county), United Kingdom £44,000 pa

Hybrid Permanent

Director of Process Innovation

This role involves leading the discovery-stage process development and analytical innovation for a novel lentiviral vector platform. Responsibilities include designing and optimizing small-scale bioreactor processes, developing analytical methods, and collaborating with discovery scientists and CMC teams to ensure tech-transfer readiness.

Proclinical United Kingdom

Hybrid Permanent