Latest regulatory affairs Jobs

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 Manager UK&I

The Regulatory Affairs Manager for the UK and Ireland leads the QRA team, ensuring regulatory compliance, post-market surveillance, and quality system adherence to ISO 13485. They act as the primary contact with UK and Irish regulatory agencies, manage import licences, and coordinate audits and inspections.

Medtronic Watford, United Kingdom £71,760 – £107,640 pa

On-site 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 - Medical Devices

This role involves leading quality assurance and regulatory affairs initiatives for medical devices within a global R&D and manufacturing environment. You'll work across European, American, and Asian regulatory standards, driving compliance and developing innovative solutions for quality systems. The position offers exposure to highly regulated industries and complex international projects.

Newton Colmore Cambridge, United Kingdom £42,000 – £46,000 pa

On-site Permanent

Regulatory Affairs Specialist

The Regulatory Affairs Specialist will ensure compliance with UK MDR and EU MDR requirements, maintain technical documentation, and support regulatory submissions for Class I and Class IIa medical devices. You will work closely with the QA Manager to improve the Quality Management System and coordinate post-market surveillance activities.

Cure Talent Upper Marlbrook, Worcestershire, B61 0RT, United Kingdom £45,000 – £50,000 pa

On-site 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

Regulatory Affairs Specialist - Medical Devices - Cambridge

This role involves providing regulatory guidance across the full product development lifecycle, supporting multidisciplinary teams in a technology-driven environment. You will interpret global regulations including ISO 13485, ISO 9001, and FDA 21 CFR 820, ensuring compliance while enabling innovation. The position is embedded in project work, offering real-time input on regulatory strategy and contributing to quality management systems across medical and non-medical sectors.

Newton Colmore Cambridge, United Kingdom

Hybrid Permanent

Regulatory Affairs Specialist

Talentmark are recruiting for a Regulatory Affairs Consultant to join a pharmaceutical company on a 6-month contract.Salary:Up to £55.59 per hour PAYE (Inside IR35).Regulatory Affairs Consultant Role:• Support regulatory activities across Europe, the Middle East and Africa for established healthcare...

Talentmark Reading, Berkshire, United Kingdom £48 – £56 ph

Regulatory Affairs Specialist

This role involves managing regulatory submissions to notified bodies, supporting post-market surveillance, and overseeing change management processes across EU, UK, and US markets. The specialist will work within a hybrid environment and contribute to maintaining compliance with FDA and other regulatory standards. The position supports a dynamic regulatory strategy in a multinational context.

Computer Futures Cluain Meala, South Tipperary, Ireland £47,478 pa

Hybrid Permanent

Regulatory Affairs Specialist

This role involves leading regulatory compliance for packaging materials and food contact applications across EMEA. You will translate complex legislation into actionable guidance, work closely with senior leadership, and support key customers on compliance issues. The position offers significant influence and exposure to evolving regulations and industry trends.

Manpower Wantage, Oxfordshire, United Kingdom

On-site Permanent

Quality & Regulatory Associate

This role involves supporting the Quality Management System (QMS) and Regulatory processes, including ISO13485 readiness and FDA 510(k) documentation. You will work closely with internal teams to maintain quality documentation, manage change controls, and promote continuous improvement.

Taylorollinson Manchester, United Kingdom £35,000 – £45,000 pa

Hybrid Permanent

Quality and Regulatory Labelling Program Manager

This role involves leading global labelling initiatives to ensure compliance with regulatory standards across various markets. The Program Manager will collaborate with cross-functional teams to manage change controls, mitigate risks, and drive continuous improvement in labelling processes.

Randstad Engineering Popley, Hampshire, RG24 9TW, United Kingdom £27 ph

Hybrid Contract

Associate Director, Regulatory Policy

The Associate Director, Regulatory Policy, provides leadership in regulatory compliance and policy, ensuring alignment with global and regional requirements. Key responsibilities include interpreting regulatory policies, developing internal guidelines, and supporting cross-functional teams to manage regulatory risks and enable informed decision-making.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

Associate Director, Regulatory Policy

The Associate Director, Regulatory Policy, provides leadership in regulatory compliance and policy, ensuring alignment with global and regional requirements. Key responsibilities include interpreting regulatory policies, developing internal guidelines, and supporting cross-functional teams to manage regulatory risks and enable informed decision-making.

Johnson & Johnson MedTech United Kingdom

On-site Permanent

Technical Writer

The Technical Writer will create and maintain technical and customer-facing documents, ensuring accuracy and up-to-date information across Regulatory Affairs, Marketing, and Technical Services. The role involves working with multiple stakeholders, managing documentation, and supporting continuous improvement initiatives.

Talentmark Burgess Hill, West Sussex, United Kingdom £264 – £331 pd

Hybrid Contract Clearance Required