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

The Regulatory Affairs Specialist will support post-market regulatory activities for medical devices, including field safety corrective actions, regulatory authority inquiries, and complaint process support. They will monitor and interpret regulatory requirements, manage regulatory documentation requests, and provide guidance to sales teams on product complaint handling and returns.

Medtronic Watford, United Kingdom £40,000 – £60,000 pa

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

Regulatory Affairs Specialist

The Regulatory Affairs Specialist will support the Quality & Regulatory team in maintaining and executing regulatory activities across a diverse product portfolio. Responsibilities include preparing technical documentation, ensuring compliance with global regulatory requirements, and coordinating audits. The role offers hands-on experience across the full product lifecycle and involves close collaboration with internal teams.

Cure Talent Uxbridge South, London, United Kingdom £40,000 – £50,000 pa

On-site 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

Internal Auditor - Public Sector Services

Internal Auditor - Public Sector Services - Cannock - HomebasedDue to recent expansion, a growing Internal Auditing Organisation is currently looking for a few Internal Auditors to help with their growing workload. The offices are based in Cannock, but the...

Newton Colmore Cannock, WS11 1DD, United Kingdom

Medical Devices Consultant - Senior Mechanical Engineer

Medical Devices Consultant - Senior Mechanical Engineer - CambridgeDue to the growth of a leading Medical Devices organisation, we are currently seeking a Senior Mechanical Engineer, Project Manager, Medical Devices Inventor, or Mechanical Design Consultant for a newly approved role....

Newton Colmore Cambridge, United Kingdom

Permanent

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

Manager, Label Strategist (Regulatory Affairs)

Label Strategy Manager (Devices) - EuropeLocation: Maidenhead/Remote (Hybrid working model)Contract: Temporary, full-time (7‑month maternity cover), starting July 2026Rate: Negotiable - circa. £60-70 per hourAn exciting opportunity has arisen for an experienced Label Strategy Manager (Devices) to join a European labelling...

Carbon 60 Maidenhead, Berkshire, United Kingdom £60 – £70 ph

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

QA and RA Manager

My client, an innovative technology business within the medical device sector, are seeking a Quality Assurance & Regulatory Affairs Manager to join their team.Working closely with senior leadership, R&D and operations, you will play a pivotal role in bringing products...

Eclectic Recruitment Impington, United Kingdom

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