Latest regulatory affairs specialist 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 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 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

Regulatory Affairs SpecialistSalary: £30,000 – £35,000 DOE plus benefitsLocation: BedfordFull-Time; 12-month Fixed Term ContractThe VacancySwiss Precision Diagnostics (SPD) is a world leader in the research, design and supply of advanced consumer diagnostic products. SPD is a joint venture between Procter...

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

Regulatory Affairs Specialist

This role involves preparing and managing regulatory submissions for medical devices, ensuring compliance with EU MDR, ISO 13485, and global standards. The specialist will maintain technical documentation, support clinical evaluations, and collaborate with cross-functional teams throughout the product lifecycle, playing a key part in product registrations and post-market surveillance.

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

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 - 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 - 6074

Manages the preparation and delivery of regulatory submissions to health authorities across multiple markets, coordinating timelines, translations, and document builds. Acts as a subject matter expert on dossier types and eCTD standards while mentoring colleagues and resolving submission-related issues. Focuses on improving efficiency through reuse of submission content across regions.

Talentmark Sandwich, Kent, United Kingdom £24 – £26 ph

Hybrid Contract Clearance Required

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

Content Compliance Specialist

This role involves managing and improving content compliance and copy review processes across EMEA markets, ensuring promotional materials meet regulatory and procedural standards. The specialist supports audit readiness, drives process efficiency, and contributes to digital innovation using AI and automation tools. Working in a multilingual, matrixed environment, they provide guidance to submitters and maintain high-quality, compliant content workflows.

Johnson & Johnson MedTech Leeds, United Kingdom £67,500 – £106,835 pa

Hybrid Permanent

Content Compliance Specialist

This role involves managing and improving content compliance and copy review processes across EMEA markets for MedTech promotional materials. The specialist ensures regulatory adherence, supports audit readiness, and drives process efficiency through digital tools, AI, and automation. They provide guidance to submitters, maintain documentation, and contribute to system enhancements in a multilingual, cross-regional environment.

Johnson & Johnson MedTech €67,500 – €106,835 pa

Hybrid Permanent

Principal Scientist – Histopathology

The role involves leading technical aspects of assay and product development in histopathology, with a focus on immunohistochemistry (IHC) slide interpretation and scoring. The Principal Scientist will guide R&D projects, mentor junior scientists, and ensure technical and commercial alignment of diagnostic tools. Work is conducted within a regulated, development-driven environment with cross-functional collaboration across quality, regulatory, and medical affairs.

Taylorollinson Newcastle upon Tyne, Tyne & Wear, NE1 4JA, United Kingdom £50,000 – £60,000 pa

On-site 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