Latest Regulatory Affairs Specialist Jobs

Spotlight

Lead Development Engineer

This role involves leading the design and development of next-generation orthopaedic implants and instrumentation. Responsibilities include creating detailed designs using CAD, FEA, and PLM, mentoring team members, managing design control documentation, and collaborating with manufacturing, quality, and regulatory teams. The position offers opportunities to work with cutting-edge technologies and contribute to impactful medical innovations.

Corin Group Cirencester, gloucestershire, United Kingdom

On-site Permanent

Regulatory Affairs Specialist

As a Regulatory Affairs Specialist, you will work within a global team to ensure medical devices meet regulatory requirements. Your responsibilities include preparing regulatory submissions, collaborating with project teams, and maintaining compliance throughout the product lifecycle.

Smith & Nephew Watford, United Kingdom

Hybrid Permanent

Regulatory Affairs Specialist

As a Regulatory Affairs Specialist, you will work across regions and products, preparing global regulatory submissions and maintaining compliance for Smith & Nephew's orthopaedic portfolio. You will collaborate with project teams to develop regulatory strategies, support product changes, and ensure adherence to international regulations.

Smith & Nephew United Kingdom

Hybrid Permanent

RA Specialist

Are you an experienced regulatory professional looking for your next long-term career move?I am partnering with an innovative, medical technology business to find a dedicated Regulatory Affairs Specialist to join their growing RAQA team on a permanent & 100% remote...

GxPeople Global United Kingdom £40,000 – £50,000 pa

Remote Permanent

Mechanical Engineer - Genomics Instrumentation - Cambridge

You will work within a multidisciplinary team to design and develop cutting-edge genomics instrumentation, contributing to high-throughput genomic workflows and precision diagnostics. Your role involves the full product lifecycle, from concept development to product launch.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Regulatory Affairs Manager IVD

This role involves leading and supporting regulatory activities for IVD products across global markets, preparing and submitting regulatory documentation, and ensuring compliance with IVDR and other regulations. You will collaborate with R&D, Quality, Clinical, and Commercial teams to provide strategic regulatory guidance and support audits and interactions with regulatory authorities.

Hays Life Sciences Hertfordshire, United Kingdom £45 – £55 ph

Remote Contract

Regulatory Affairs Assistant

The Regulatory Affairs Assistant will support the submission and maintenance of global regulatory approvals, assist with regulatory submissions for new markets, and handle customer audit and tender requests. This role is part of a growing RA function within a global manufacturing organization focused on innovation and patient safety.

L-ev8 Recruitment Ltd Plymouth, Devon, United Kingdom £25,000 – £30,000 pa

On-site Permanent

Regulatory Affairs Manager

Cure Talent are delighted to be partnered with a global medical device organisation recognised as one of the most established and successful healthcare companies in the world. With a diverse international footprint and a strong pipeline of innovation, the business...

Cure Talent Curbridge, Oxfordshire, United Kingdom

Head of Quality Assurance and Regulatory Affairs

Evolve are partnering with a fast-growing organisation to appoint a Head of Quality Assurance & Regulatory Affairs. This is a strategic leadership role where you will drive quality and regulatory excellence, support global expansion, and work cross-functionally to ensure consistently...

Evolve Selection London, United Kingdom

QA/RA Assistant/Manager

This role involves supporting quality, regulatory, and information security processes in a growing laboratory setting. Responsibilities include maintaining the Integrated Management System, ensuring compliance with various standards, managing controlled documentation, and working closely with technical teams to maintain quality standards.

Guilford Street Laboratories Liverpool, Merseyside, United Kingdom £35,000 – £45,000 pa

On-site Permanent

Head of QARA

Cure Talent are delighted to be partnered with an innovative medical technology company transforming access to ear and hearing healthcare. Operating at the intersection of medical devices and software, the business is scaling its global presence and is now looking...

Cure Talent Marylebone High Street, London, United Kingdom £80,000 – £90,000 pa

On-site Permanent

Process Engineer, Validation

The Process Engineer, Validation leads and executes validation activities for new product ranges and changes to existing medical devices. They ensure all manufacturing processes, equipment, and test methods meet internal and external regulatory standards, working closely with cross-functional teams and external partners. The role involves developing validation strategies, authoring protocols, conducting risk assessments, and supporting regulatory submissions.

OrganOx Oxford, United Kingdom

On-site Permanent

Patient Safety Partner

The Patient Safety Partner will support individual case safety reports, assess pharmacovigilance requirements, and manage local safety risks within ophthalmology. They will also assist with global safety solutions, product launches, and cross-functional team collaboration, contributing to audits and continuous improvement activities.

Talentmark Welwyn Garden City, Hertfordshire, AL8 6TP, United Kingdom £50 – £66 ph

Hybrid Contract

Medical Advisor

Want a 3D Career? Join Norgine.At Norgine, our colleaguesDare themselves to be different and try new things,Drive to achieve their goals and beyond, andDevelop themselves and their community.We call it the3D career at Norgine and it offers you a fully-rounded...

Norgine Uxbridge, UB8 1SB, United Kingdom

Hybrid

Compliance Engineer

The Compliance Engineer will be responsible for conducting and overseeing compliance and testing for medical products, ensuring they meet UK, USA, and EU standards. Key tasks include operating test equipment, writing reports, and driving continuous improvement in R&D.

JASA TALENT Cheltenham, Gloucestershire, United Kingdom £45,000 – £50,000 pa

On-site Permanent

Quality & Regulatory Specialist

As a Quality & Regulatory Specialist, you will support clients in developing medical devices with a strong software focus, ensuring they meet regulatory requirements and quality standards. Your role involves creating and reviewing technical documentation, educating clients on regulatory needs, and collaborating with software engineers and senior stakeholders to deliver practical solutions.

Vero Hr Cambridge, Cambridgeshire, United Kingdom £45,000 – £55,000 pa

Remote Permanent Flexible