Latest Regulatory Affairs Specialist Jobs

Director, Regulatory Data Office Leader

This role involves leading a global team of data stewards and overseeing the Regulatory Data Hub to ensure high-quality regulatory data for business intelligence and decision-making. The Director will establish data governance policies, collaborate across R&D and IT, and drive regulatory data transformation initiatives.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Director, Regulatory Data Office Leader

The Director, Regulatory Data Office Leader, will lead a global team of data stewards and oversee the Regulatory Data Hub (RDH) to ensure high-quality regulatory data for business intelligence and decision-making. The role involves data governance, regulatory compliance, and collaboration with R&D, IT, and data science teams to drive digital transformation and AI adoption.

Johnson & Johnson MedTech

Electronics Design Engineer

Design and develop electronic circuits and PCBs for medical devices used in organ preservation technology, with full lifecycle responsibility from concept to manufacturing. Work closely with cross-functional teams to ensure compliance with safety and regulatory standards like IEC 60601. Focus on reliability, integration, and verification within a regulated medical device environment.

OrganOx Oxford, United Kingdom

On-site Permanent

Senior Design Assurance Engineer

The Senior Design Assurance Engineer leads risk management activities across the full product lifecycle for Class II and III medical devices, ensuring compliance with ISO 14971 and regulatory standards. This role involves developing and maintaining risk documentation, facilitating cross-functional risk reviews, and integrating risk controls into design verification. The position supports ongoing product improvement by monitoring post-market data and contributing to quality processes within a growing medical technology team.

OrganOx Oxford, United Kingdom

On-site Permanent

Clinical Applications Specialist (Monitoring Analytics) - London & South-Central region

This role involves promoting Philips Healthcare products and systems, providing comprehensive training to customers, and ensuring optimal usage and customer satisfaction. The Clinical Applications Specialist will work closely with account and product managers to achieve modality results and support new product launches.

Philips Rushmoor, GU14 7JT, United Kingdom

Quality Engineer

A Quality Engineer will lead quality initiatives across a manufacturing value stream, providing technical support to resolve nonconformances and drive process improvements using statistical methods and root cause analysis. The role involves conducting Measurement System Analysis, process validation, and risk assessments while ensuring compliance with regulatory standards. Collaboration with manufacturing, R&D, and NPI teams is key to embedding quality into product lifecycle processes.

Smith & Nephew United Kingdom

Procurement Lead

The Procurement Lead will manage global supplier relationships and contract manufacturers, focusing on cost optimisation, supply continuity, and commercial negotiations within a regulated medical products environment. The role involves leading RFx processes, driving cost improvement initiatives, and collaborating with cross-functional teams on change controls, product transfers, and supplier performance. A strong background in direct materials procurement and contract manufacturing is essential.

Butler Ross Leverstock Green, Hertfordshire, HP3 8QG, United Kingdom £55,000 – £60,000 pa

Test Engineer

This role involves designing and implementing quality test procedures for both software and hardware components of medical devices. Responsibilities include attending design meetings, writing test plans, analyzing opportunities for automated testing, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa

On-site Permanent

Test Quality Assurance Engineer

This role involves designing and implementing quality test procedures for both software and hardware in medical device products. Responsibilities include attending design meetings, writing test plans, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa

On-site Permanent

Quality Engineer

This role involves hands-on quality engineering within a regulated medical device manufacturing environment, focusing on improving the Quality Management System (QMS) through data-driven insights and direct collaboration with production teams. The engineer will lead non-conformance investigations, support audits, drive continuous improvement initiatives, and ensure compliance with ISO 13485 and ISO 14971 standards. Emphasis is placed on practical, floor-based problem-solving to embed a quality-first culture across operations.

Aurora Life Sciences Leeds, West Yorkshire, United Kingdom £45,000 – £50,000 pa

On-site Permanent

R&D Consultant - Drug Delivery Device Design - Cambridge

This role involves leading the design and development of next-generation drug delivery devices, working closely with multidisciplinary teams to translate early-stage concepts into robust, manufacturable solutions. Responsibilities include hands-on involvement in concept generation, prototyping, and risk management, as well as mentoring junior colleagues and advising clients on technical decisions.

Newton Colmore Cambridge, United Kingdom

On-site Permanent

PhD Level Ultrasound Technology Consultant - Cambridge

This role involves driving the development of next-generation surgical and interventional devices using advanced ultrasound technology. Responsibilities include leading high-impact technical programmes, collaborating with partner organisations, and applying scientific expertise from feasibility studies to market preparation.

Newton Colmore Cambridge, United Kingdom

On-site Permanent

Senior Mechanical Engineer

Design and develop advanced electro-mechanical systems for next-generation medical technology, from concept through to manufacture. Work within a multidisciplinary team to solve complex engineering challenges, ensuring compliance with regulatory standards and driving continuous improvement. Utilise SolidWorks and engineering best practices in a collaborative, innovative environment focused on real-world impact.

AES Ely, Cambridgeshire, United Kingdom £50,000 – £75,000 pa

Hybrid Permanent

Lead Production Engineer

Leads a team of five production engineers to drive industrialisation, process improvement, and new product introduction within a regulated medical device environment. Focuses on evolving production systems through automation, Lean methodologies, and design-for-manufacture principles while ensuring quality, scalability, and regulatory compliance. Plays a central role in transitioning next-generation products from development into robust, efficient production.

PDQ Engineering Recruitment & Training Services Lt Abingdon, Oxfordshire, OX14 5BH, United Kingdom £50,000 – £55,000 pa

Technical Service Lead

Join us in making sure no one is left without a voice.At Smartbox, our assistive technology empowers people with disabilities who experience speech difficulties to express themselves, connect with others, and live more independent lives.We’re proud to be a global...

Smartbox Assistive Technology Malvern Link, Worcestershire, WR14 1NB, United Kingdom £40,000 – £50,000 pa