Latest Regulatory Affairs Specialist Jobs

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 - Innovation

This role involves providing regulatory expertise for in vitro diagnostic (IVD) and medical device innovation projects, from concept to commercialisation. The specialist will support global regulatory strategies, ensure compliance with standards like IVDR and MDR, and collaborate with cross-functional teams. The position also includes assessing emerging regulations and supporting submissions to notified bodies and regulatory authorities.

SPD Development Company Ltd Cardington, Bedfordshire, United Kingdom £35,000 – £40,000 pa

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

Senior Regulatory Affairs Specialist

This role involves managing regulatory compliance for advanced wound care medical devices throughout their lifecycle, including preparing global regulatory submissions, guiding product development teams, and liaising with regulatory authorities. The specialist ensures adherence to standards such as ISO 13485, FDA 21 CFR Part 820, cGMP, and cGDP, while reviewing product documentation and supporting continuous improvement. Based in Hull, the position operates within a collaborative, global team environment focused on bringing innovative healthcare products to market.

Smith & Nephew United Kingdom

Hybrid Permanent

Senior Source Regulatory Compliance Specialist

The Senior Source Regulatory Compliance Specialist is responsible for ensuring suppliers, contract manufacturers, and sourced materials comply with regulatory requirements and internal policies. Key responsibilities include executing supplier audits, managing compliance documentation, and supporting continuous improvement initiatives in supplier compliance.

Johnson & Johnson MedTech Leeds, United Kingdom

Senior Source Regulatory Compliance Specialist

The Senior Source Regulatory Compliance Specialist is responsible for ensuring suppliers and sourced materials comply with regulatory requirements and quality standards. Key responsibilities include executing supplier audits, managing compliance documentation, and partnering with cross-functional teams to maintain audit readiness and supply continuity.

Johnson & Johnson MedTech

Senior Field Clinical Research Specialist

Acts as the primary field contact for clinical trial sites, managing site activation, training, participant enrollment, and data quality. Ensures compliance with regulations and supports cross-functional teams across Europe. Focuses on renal denervation therapy within interventional cardiology, working closely with investigators and internal stakeholders to deliver high-quality clinical studies.

Medtronic Watford, United Kingdom £50,400 – £75,600 pa

Senior Field Clinical Research Specialist

This role involves managing clinical trial sites for Medtronic's Renal Denervation therapy, ensuring studies are conducted efficiently and in compliance with regulations. The specialist will build relationships with investigators, support data collection, and coordinate trial activities across Europe, with frequent travel required. The position supports transformative hypertension treatments within a global medical technology leader.

Medtronic Netherlands £50,400 – £75,600 pa

Quality Engineer - Medical Devices & Precision Manufacturing - Rotherham

This role involves ensuring quality and compliance across the full manufacturing lifecycle, from incoming materials to batch release, within a regulated environment. The Quality Engineer will maintain and improve the Quality Management System (QMS), lead root-cause analysis for non-conformances, support audits, and work closely with production and engineering teams to drive continuous improvement. The position is based in Rotherham and operates on a compressed workweek schedule.

Vested Talent Rotherham, South Yorkshire, United Kingdom £40,000 – £44,000 pa

Senior Compliance Specialist, EMEA

The Senior Compliance Specialist, EMEA, is responsible for ensuring that all HCP and HCO interactions comply with applicable laws, regulations, and industry codes. Key responsibilities include reviewing and approving HCP engagement activities, managing the sponsorship review process, and providing compliance training. The role involves close collaboration with various business functions to maintain a strong culture of integrity and ethical business conduct.

Nicholas Howard Ltd London, United Kingdom

Regulatory Affairs Associate

This role involves supporting regulatory compliance and product registrations for medical devices, medicines, and food supplements across EMEA markets. The candidate will prepare submissions, maintain licences, interpret regulations, and collaborate with cross-functional teams and external stakeholders. It offers broad international exposure within a hybrid-working environment.

Recruitment Solutions (Folkestone) Ltd Folkestone, Kent, United Kingdom

Director, Regulatory Affairs, Europe

Leads the European Regulatory Affairs team at GE HealthCare, defining regulatory strategy and ensuring compliance with EU MDR and UK MDR for medical devices. Oversees CE and UKCA marking, manages interactions with Notified Bodies and Competent Authorities, and drives regulatory alignment across quality, legal, and product teams. Focuses on strategic planning, postmarket compliance, and industry engagement in a global healthcare technology environment.

GE HealthCare Chalfont St Giles, Buckinghamshire, United Kingdom

Senior Director Medical Affairs, Oncology Precision Diagnostics

This role involves leading the global Medical Affairs strategy for QIAGEN's Oncology Precision Diagnostics portfolio, driving scientific excellence and enabling the adoption of precision medicine solutions. Responsibilities include shaping medical strategy, fostering innovation, and building strong external relationships with key stakeholders in oncology and pharmaceuticals.

QIAGEN Manchester, United Kingdom

Project Manager

This role involves leading the end-to-end development programme for a next-generation medical device, coordinating cross-functional teams across engineering, clinical, regulatory, and supply chain. The Project Manager will own the Integrated Development Plan, ensure compliance with ISO 13485 and FDA 510(k) requirements, manage third-party vendors, and maintain the Design History File. It is a high-visibility position central to scaling the product through regulatory submission and into commercial launch.

GxPeople Global London, United Kingdom £80,000 – £90,000 pa

Regulatory Business Analyst

This role involves gathering and translating regulatory, quality, and R&D business requirements into digital solutions within a global transformation programme. The analyst will lead discovery sessions, map complex regulatory workflows, and convert needs into user stories and acceptance criteria, working closely with IT and compliance teams. A key focus is supporting the evolution of regulatory systems with an aim to transition into a Technical Product Owner role.

New Appointments Group London, United Kingdom

Hybrid Permanent