Latest regulatory affairs 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

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

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 £40,000 – £60,000 pa

On-site Permanent

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

Quality Engineer

The Quality Engineer is responsible for developing, implementing, and maintaining quality plans, metrics, processes, and systems to ensure Azenta Life Science products consistently meet the highest standards of reliability, performance, and regulatory compliance.This role serves as a technical quality leader,...

Azenta Life Sciences Partington, Manchester, United Kingdom

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 £20,000 – £30,000 pa

On-site Permanent

Biomedical Field Service Engineer

This role involves performing preventative maintenance and repairs on medical equipment in UK hospitals, ensuring minimal disruption to hospital operations. You will work closely with the site manager, maintain service documentation, and interact with customers and OEM staff, requiring strong communication and technical skills.

Focus Resourcing United Kingdom £30,000 – £45,000 pa

On-site Permanent

Quality Engineer

Quality EngineerA Quality Engineer is needed for a fast-growing engineering and manufacturing business supplying into a highly regulated sector. They are looking to appoint a Quality Engineer to strengthen their quality capability and support continued growth, improvements, new customer demand,...

White Label Recruitment Leeds, United Kingdom

Head of Compliance - Medical Device

This senior leadership role involves shaping compliance strategy, strengthening regulatory frameworks, and overseeing global compliance activities for medical devices. You will provide expert guidance, ensure regulatory alignment, and drive quality-related activities in a fast-paced, evolving environment.

SRG United Kingdom

On-site Permanent

Site Director - Medical Device Manufacturing

The Site Director will lead operations at a medical device manufacturing facility in Ashford, Surrey. Key responsibilities include integrating new product lines, optimizing site layout, and ensuring compliance with ISO 13485 standards. The role involves close collaboration with Quality, Regulatory, R&D, Supply Chain, and Manufacturing teams to drive process improvements and align with strategic objectives.

Michael Page Engineering & Manufacturing Surrey, United Kingdom

On-site Permanent

Sample Management Technician York

Our client requires a Sample Management Technician for an 8 month duration initially to work within the Clinical Trials Specimen Management team. You will be responsible for the handling of clinical trials specimens and their associated data, including managing human...

Coyles York, YO1 8RS, United Kingdom