Latest Regulatory Affairs Specialist Jobs

Principal Market Development and Strategic Marketing Specialist

Lead market development for cardiac conduction system pacing and bradycardia/CRT-P therapies across Western Europe, translating clinical evidence into actionable strategies and customer tools. Drive product launches, adoption, and cross-functional alignment with country teams, sales, and clinical stakeholders. Focus on removing clinical, operational, and perception barriers to therapy uptake through scalable frameworks and customer-centric execution.

Medtronic

Principal Market Development and Strategic Marketing Specialist

This role involves leading market development and strategic marketing for cardiac conduction system pacing and bradycardia/CRT-P therapies across Western Europe. The specialist will drive therapy adoption, launch execution, and translate clinical evidence into actionable tools and value narratives. Collaboration with cross-functional teams and country marketing units is central to removing adoption barriers and scaling regional growth.

Medtronic €53,600 – €80,400 pa

Medical Safety Officer - PALM

This role involves leading the medical safety assessment of pharmaceutical products throughout their lifecycle, with a focus on signal detection, risk management, and regulatory compliance. The Medical Safety Officer provides scientific leadership across cross-functional teams, contributes to key regulatory documents, and communicates safety findings to internal stakeholders and health authorities. The position requires strong expertise in pharmacovigilance, clinical trial safety, and global regulatory standards.

Johnson & Johnson MedTech

Medical Safety Officer - PALM

This role involves leading the safety assessment and benefit-risk oversight of pharmaceutical products across their lifecycle, with a focus on proactive risk management and regulatory compliance. The Medical Safety Officer provides medical expertise to cross-functional teams, contributes to clinical and regulatory documentation, and communicates safety findings to internal leadership and external health authorities. Key responsibilities include signal detection, risk mitigation strategy design, and medical oversight of safety evaluations.

Johnson & Johnson MedTech

Senior Development Technologist

This role involves leading technical strategy and project delivery for new product development in the medical device sector, with a focus on design control, regulatory compliance, and manufacturing process innovation. The individual will manage technical teams, ensure adherence to quality standards, and support the full product lifecycle from concept to commercialization within a regulated environment.

Smith & Nephew United Kingdom

Medical Devices Project Leader - Warwick

Lead the development of medical devices from concept to commercial launch within a multidisciplinary engineering team. Drive project execution with a focus on high-volume manufacturability, particularly using injection-moulded plastics, while mentoring junior engineers and ensuring regulatory and design compliance. Play a key role in shaping technically robust, patient-focused medical technologies in a fast-paced environment.

Newton Colmore Warwick, United Kingdom

Hybrid Permanent

Product Support Engineer

The role involves providing advanced technical support for a global fleet of sophisticated electro-mechanical robotic systems used in healthcare. You'll conduct root cause analysis on complex product issues, develop diagnostic procedures, and act as a technical liaison between engineering, quality, regulatory, and field service teams. The position emphasizes continuous improvement, regulatory compliance, and influencing future product design within a highly regulated environment.

AES Impington, Cambridgeshire, United Kingdom £40,000 – £50,000 pa

Mechanical Design Engineer

Design and develop complex injection moulded plastic components and polymer-based medical devices, focusing on scalability, manufacturability, and regulatory compliance. Lead concept-to-production design projects involving robotics and mechatronics, working closely with manufacturing partners and cross-functional teams. Engage in hands-on prototyping, materials selection, and design validation within a regulated medtech environment.

Innovo Global Talent Warrington, Cheshire, United Kingdom £35,000 – £45,000 pa

Medical Systems Engineer

This role involves capturing and managing requirements for medical devices, ensuring compliance with regulatory standards in both hardware and software engineering. The engineer will design and implement development processes, with a focus on best coding practices and test procedures. Work is primarily remote, with occasional travel to Cheltenham.

Circuit32 Recruitment Cheltenham, Gloucestershire, United Kingdom £50 – £65 ph

Remote Contract

Head of Medical Engineering / EBME

Leads and develops a multidisciplinary medical engineering team, ensuring safe and compliant management of medical devices across a complex healthcare environment. Oversees equipment lifecycle, maintenance, procurement, and asset management while driving service transformation and performance improvement. Provides strategic direction and assurance on medical device governance and regulatory compliance to senior stakeholders.

Linea United Kingdom £63,000 – £78,000 pa

On-site Permanent

Scientist

The Scientist role involves hands-on R&D support for new product development, line extensions, and design changes, focusing on sterile, single-use medical devices. Responsibilities include laboratory testing, verification, validation, and maintaining regulatory documentation.

Cure Talent Crewe, Cheshire, United Kingdom £28,000 – £34,000 pa

On-site Temporary

Quality Assurance Manager, Medical Device & Combination Products

This role involves providing quality oversight for medical device and combination product programs across development and sustaining phases. The individual will lead complaint investigations, ensure compliance with design controls and regulatory standards, and support cross-functional teams in risk-based decision-making. Focus areas include change management, post-market surveillance, and continuous improvement of quality systems in a highly regulated environment.

Pfizer Cambridge, Cambridgeshire, United Kingdom

Technical Writer

Produces and maintains technical documentation for sequencing devices, ensuring accuracy, regulatory compliance, and clarity for customers and external bodies. Works within a quality-managed environment to support product releases and safety standards. Translates complex technical and scientific information into accessible content.

Oxford Nanopore Technologies Oxford, United Kingdom

Bioinformatics Software Test Engineer

This role involves testing bioinformatics software within clinical and biopharma analysis workflows, focusing on the EPI2ME platform. The engineer ensures regulatory compliance with SaMD standards, verifies correct implementation of new features, and identifies critical bugs prior to release. Testing must be thoroughly documented to maintain audit-readiness and adherence to IEC 62304, ISO 13485, and ISO 14971.

Oxford Nanopore Technologies Oxford, United Kingdom

On-site Permanent

Senior Product Development Scientist

Leads product development projects in the medical devices sector, focusing on assay development, optimisation, and lifecycle management within regulated environments. Responsible for data analysis, regulatory compliance, equipment validation, and mentoring junior staff. Works in a collaborative, innovation-driven setting with a strong emphasis on quality and continuous improvement.

STEM Recruitment Queen Street, Edinburgh, United Kingdom