Latest regulatory affairs Jobs

Regulatory Affairs Assistant

The Regulatory Affairs Assistant will provide administrative, operational, and compliance support to the Regulatory Affairs team, ensuring accurate data and documentation, supporting team processes, and maintaining compliance with regulatory standards. The role involves a broad range of activities, including regulatory file compilation, database management, project coordination, and administrative support to the Head of Regulatory and the team.

AstraZeneca London, United Kingdom

On-site Permanent

Regulatory Affairs Manager

Regulatory Affairs ManagerType: PermanentLocation: Pancras Square, LondonIntroduction to roleDeliver and maintain competitive licences for the UK, driving regulatory strategy for new initiatives and ensuring regulatory compliance for defined product and project responsibilities, including project leadership. Achieve timely delivery of clinical...

AstraZeneca London, United Kingdom

Regulatory Affairs Specialist - Medical Devices

This role involves leading quality assurance and regulatory affairs initiatives within a global medical devices company, working across European, American, and Asian regulatory standards. You will develop and implement solutions for compliance and management systems in a highly technical R&D and manufacturing environment. The position offers exposure to emerging regulated industries and complex, international projects.

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

On-site Permanent

Regulatory Affairs Specialist - Medical Devices - Cambridge

This role involves providing regulatory expertise to guide product development across medical and non-medical technologies, ensuring compliance with international standards such as ISO 13485, FDA 21 CFR 820, and ISO 9001. The specialist will work embedded within project teams, interpreting evolving regulations, supporting quality systems, and enabling innovation while maintaining regulatory alignment throughout the product lifecycle.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Regulatory Affairs Specialist

This role involves preparing and managing regulatory submissions for medical devices, ensuring compliance with EU MDR and ISO 13485 standards. The specialist will maintain technical documentation, support clinical evaluations, and collaborate with cross-functional teams throughout the product lifecycle. A key focus is staying current with global regulatory changes and ensuring continuous market access through timely renewals and post-market surveillance.

SRG Perivale, London, UB6 8DD, United Kingdom £50,000 – £60,000 pa

On-site Permanent

Regulatory Affairs Specialist

This role involves maintaining technical documentation and ensuring compliance with UK and EU MDR regulations for Class I and IIa medical devices. The specialist will support regulatory submissions, post-market surveillance, and quality management system development within a regulated environment. Collaboration with the QA Manager and ongoing product lifecycle support are key aspects of the position.

Cure Talent Upper Marlbrook, Worcestershire, B61 0RT, United Kingdom £45,000 – £50,000 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, Oxfordshire, United Kingdom £85,000 – £95,000 pa

Regulatory Affairs Specialist

The role involves providing technical regulatory support for the international distribution of diagnostic products, ensuring compliance with CE marking and global medical device regulations. Responsibilities include validating product claims, maintaining up-to-date documentation, and reviewing complaints for regulatory reportability. The position is based at the Innovation Centre in Bedford with hybrid working options.

Swiss Precision Diagnostics GmbH Cardington, Bedfordshire, United Kingdom £30,000 – £35,000 pa

Hybrid Contract

Global Regulatory Affairs Associate Director (Cardio-Metabolic)

This role involves leading the development and submission of regulatory documents, providing strategic direction, and negotiating with health authorities to expedite approvals. The position also focuses on ensuring compliance and timely approval of new and marketed products, serving as a regulatory liaison throughout the product lifecycle.

Novartis London, United Kingdom

Hybrid Permanent

Global Regulatory Affairs Associate Director (Cardio-Metabolic)

This role involves leading the development and submission of regulatory documents, providing strategic direction, and negotiating with health authorities to expedite approvals. The position also focuses on aligning regional regulatory approaches with global objectives and managing Health Authority interactions.

Novartis

Hybrid Permanent

Senior Manager - CMC Regulatory Affairs Biopharm Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, mentoring staff, and engaging with external agencies to ensure compliance and expedite submissions.

GSK Canterbury, United Kingdom

On-site Permanent

Senior Manager - CMC Regulatory Affairs Biopharm Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, and mentoring staff. The position requires a strong understanding of regulatory requirements and the ability to communicate complex issues across departments and with external agencies.

GSK

On-site Permanent

Head of Global Regulatory Affairs and Strategy

This senior leadership role involves defining and optimizing global regulatory strategies for drug development programs, building a regulatory team and systems, and implementing quality, pharmacovigilance, and medical writing frameworks. The role leverages AI to streamline regulatory workflows and ensure rapid global approval of products.

Isomorphic Labs Cambridge, United Kingdom

On-site Permanent

Associate Director, CMC Regulatory Affairs

This role involves leading the development and implementation of CMC regulatory strategies for small molecule drugs in global clinical trials. Responsibilities include managing CMC submissions, providing regulatory guidance, and supporting cross-functional teams in navigating international regulations.

Recursion London, W1C 2QP, United Kingdom £88,200 – £111,100 pa

Hybrid Permanent Flexible

Associate Director, CMC Regulatory Affairs, International

This role involves developing and implementing CMC regulatory strategies for international submissions, providing guidance on regulatory CMC aspects, and leading discussions with health authorities. The candidate will also support the creation of CMC submission templates and offer interpretations of regulatory guidance documents, ensuring compliance and efficient delivery of high-quality regulatory documentation.

Moderna London, United Kingdom

On-site Permanent