Latest Regulatory Affairs Specialist Jobs

Associate Clinical Project Manager

This role involves supporting the delivery of clinical studies from protocol development to final reporting. Responsibilities include maintaining the Trial Master File, coordinating cross-functional teams, and ensuring regulatory compliance. The position is ideal for someone early in their clinical research career who enjoys organization and collaboration.

VRS UK Slough, Berkshire, United Kingdom £43,000 – £50,000 pa

On-site Permanent

Business Development Manager - International

About Skin AnalyticsSkin Analytics is an award-winning, health tech company that works with dermatology teams to deploy world-leading AI driven solutions for the diagnosis, triage and referral of skin cancer and general dermatology conditions. Our offering is rapidly expanding into...

Skin Analytics London, United Kingdom

Hybrid Permanent

Clinical Trials - Business Development Manager

This role involves identifying and developing business opportunities in the clinical trial sector, leading negotiations, and serving as the primary contact for strategic clients. The manager will work on comprehensive clinical programmes, manage procurement, and ensure compliance with MHRA protocols and guidelines.

B&S Group (Laxmico Ltd) Ruislip, London, HA4 8BD, United Kingdom £40,000 – £45,000 pa

On-site Permanent

R&D Design Engineer

The R&D Design Engineer will focus on the design, prototyping, and development of medical devices, ensuring they meet regulatory requirements and are ready for market. Responsibilities include risk analysis, process development, and introducing new technologies and materials.

Real Limerick, Limerick County, Ireland £35 – £39 ph

On-site Contract

Systems Engineer - Embedded and Hardware

This senior role involves leading the electronics and software workstream for IVD medical devices, ensuring robust system architecture, supplier governance, and regulatory compliance. Responsibilities include third-party oversight, design controls, verification, and validation, as well as cross-functional integration and risk management.

Swiss Precision Diagnostics GmbH Cardington, Bedfordshire, United Kingdom £60,000 – £70,000 pa

On-site Permanent

Head of Research and Development

We’re partnering with a market-leader in the Ophthalmology sector, who are looking to recruit an experienced Head of R&D (Research & Development)!The successful candidate will lead R&D strategy, manage a multidisciplinary team, and work closely with key internal functions to...

Evolve Selection Cambridge, Cambridgeshire, United Kingdom

Remote Permanent

Senior Scientist

This role involves hands-on laboratory work, prototype development, and analytical method design for next-generation medical devices. You will work closely with multidisciplinary teams, including R&D, Quality, Regulatory, and Commercial functions, to innovate and develop cutting-edge products.

L-ev8 Recruitment Ltd Plymouth, Devon, United Kingdom £40,000 – £48,000 pa

On-site Permanent

Product Development Scientist

Cure Talent are delighted to be partnered with an established medical device manufacturer as they appoint a Product Development Scientist to join their R&D function on an initial 12 month fixed term contract.This is offered on an initial 12 month...

Cure Talent Cheshire, United Kingdom £30,000 – £32,000 pa

Systems Engineer - Automation

As Systems Engineer, you will manage development lifecycle involvement to provide Automated Robotic sample storage systems to deliver cutting edge scientific applications and integrated platforms for biological sample and clinical intelligence.Systems Engineer provide the cohesion and co-ordination between engineering and...

Azenta Life Sciences Partington, Manchester, United Kingdom

Senior Systems Engineer

As Senior Systems Engineer / Senior Product Development Engineer you will manage development lifecycle involvement to provide Automated Robotic sample storage systems to deliver cutting edge scientific applications and integrated platforms for biological sample and clinical intelligence.Systems Engineer provide the...

Azenta Life Sciences Partington, Manchester, United Kingdom

Clinical Trials Associate

The Clinical Trials Associate will manage Trial Master File (TMF) activities, ensure regulatory compliance, and support the delivery of clinical studies. Responsibilities include maintaining TMF, coordinating documentation, and assisting with site visits and data management.

SRG Hitchin, Hertfordshire, SG5 1HP, United Kingdom

On-site Permanent

Quality Engineer, Compliance

This role involves leading design control and risk management activities for medical device and combination product programmes, ensuring compliance with global regulatory standards. You will collaborate closely with development teams, external partners, and suppliers to maintain audit-ready documentation and support regulatory submissions.

Next Phase Recruitment Cambridge, Cambridgeshire, United Kingdom

Hybrid Permanent

Formulation and Application Specialist

The Formulation & Application Specialist will develop and scale up new formulations for healthcare and regulated consumer products. Responsibilities include designing formulations, conducting stability studies, and supporting scale-up activities. The role involves close collaboration with cross-functional teams and requires a strong background in formulation science and product development.

SRG Halifax, West Yorkshire, HX1 1TH, United Kingdom

On-site Permanent

Pharmaceutical Quality Engineer

The role involves providing quality engineering support across manufacturing, validation, and supply chain operations, ensuring compliance with GMP and GDP standards. Key responsibilities include leading deviation investigations, managing CAPA processes, and supporting internal and external audits. The position also focuses on continuous improvement and collaboration with cross-functional teams.

Smart4Sciences Cheshire, United Kingdom

On-site Contract Flexible

Junior Biomedical Field Engineer

The Junior Biomedical Field Engineer will perform preventative maintenance and repairs on medical equipment in UK hospitals, ensuring minimal disruption to hospital operations. You will support the site manager, maintain service documentation, and interact with customers and OEM staff, while adhering to safety and regulatory standards.

Focus Resourcing United Kingdom

On-site Permanent