Latest regulatory affairs specialist Jobs

Senior Firmware Engineer - Complex Problem Solving

This role involves leading electronics and firmware-focused research for highly complex defence and security projects. You will collaborate with physicists, mechanical engineers, and other electronics engineers in a top-secret, world-class lab environment, with a focus on developing innovative devices and applications.

Newton Colmore Cambridge, United Kingdom

On-site Permanent Clearance Required

Electronics Engineer Consultant - Security Clearance

Electronics Engineer Consultant - Security Clearance - CambridgeA new design consultancy, based in Cambridge, are currently looking for a Electronics Engineer Consultant to add to the team of experienced experts, specifically with a focus on security cleared projects.Although this is...

Newton Colmore Cambridge, United Kingdom

Post Doctoral Researcher, Evaluation & Standards in Clinical Operations

This role involves developing evaluation frameworks and rubrics for AI agents in clinical operations and global development. Responsibilities include designing quality dimensions, running human evaluation protocols, building benchmark datasets, and partnering with AI engineering teams to improve AI systems in specialized clinical contexts.

Johnson & Johnson MedTech Belgium

On-site Permanent

Post Doctoral Researcher, Evaluation & Standards in Clinical Operations

This role involves developing and implementing evaluation frameworks for generative AI agents used in clinical operations and global development. Responsibilities include designing quality dimensions, running human evaluation protocols, and building benchmark datasets to ensure AI systems meet the standards required by clinical and regulatory experts.

Johnson & Johnson MedTech

On-site Permanent

Regulatory Specialist - Chemicals

This role involves ensuring compliance with global chemical regulations by managing classification, labelling, and safety data documentation. The specialist will maintain and update safety data sheets and labels in line with GHS and regional requirements, analyse regulatory data, and support cross-functional projects. Work includes resolving data inconsistencies in SAP EHS and improving compliance processes within a close-knit team.

SRG Essex, United Kingdom £36,000 – £43,000 pa

Hybrid Permanent

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

Medical Device Programme Lead

Balance technical, regulatory and commercial challenges in this fulfilling roleThis highly regraded Cambridge-based medical technologies company is seeking a proven engineering leader to help guide high-value development programmes from concept through to transfer to manufacture. Your leadership will accelerate development...

ECM Selection Cambridge, United Kingdom

Quality Control Release Specialist 2

This role involves ensuring compliance with regulatory requirements and company procedures for the release of manufactured medical products. Responsibilities include leading the coordination and training of QC Release personnel, managing quality processes, and supporting continuous improvement initiatives.

Smith & Nephew Goole, United Kingdom

On-site Permanent

QC Release Specialist 2

Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.Smith+Nephew is hiringQC Release Specialist 2 .The Quality Compliance release team is focused on ensuring that Smith + Nephew complies with key regulatory requirements and Smith...

Smith & Nephew Goole, United Kingdom

Scientist

The Scientist role involves reviewing clinical data, writing technical reports, and ensuring medical devices meet regulatory requirements for CE marking and global approval. You will collaborate with a scientific and clinical team, prepare high-quality reports, and manage changing priorities in a fast-paced environment.

Peopleforce Recruitment Ltd Witney, Oxfordshire, United Kingdom £23 ph

On-site Permanent

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

Quality Engineer

As a Quality Engineer, you will drive quality excellence in a regulated manufacturing environment, leading improvement initiatives, compliance efforts, and problem-solving. You will collaborate with cross-functional teams to ensure product quality, process performance, and regulatory compliance, using structured methodologies and statistical analysis.

Consortium Professional Recruitment Hessle, East Riding Of Yorkshire, United Kingdom £45,000 – £50,000 pa

On-site Permanent

Associate Director, Toxicology

This role involves leading and developing a toxicology function within a highly regulated environment, supporting forensic toxicology services for the UK Criminal Justice System. Responsibilities include strategic planning, quality management, and driving innovation and process improvements.

Talentmark Warrington, Cheshire, United Kingdom £65,000 – £90,000 pa

On-site Permanent

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

The Quality Engineer will lead root cause investigations, drive corrective actions, and support new product introductions in a regulated manufacturing environment. They will work closely with cross-functional teams to ensure quality compliance and continuous improvement.

Owen Daniels Coventry, United Kingdom £40,000 – £45,000 pa

On-site Permanent