Latest regulatory affairs specialist Jobs

Experienced Regulatory Affairs Professional EMEA

This role involves developing and executing regulatory strategies for solid tumour pharmaceutical products across Europe, the Middle East, and Africa. The professional will support clinical trial applications, marketing authorisation submissions, lifecycle management, and engagement with health authorities, working closely with cross-functional teams. The position requires strong regulatory expertise, project management, and the ability to navigate complex regional requirements in oncology.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Experienced Regulatory Affairs Professional EMEA

This role involves developing and executing regulatory strategies for solid tumour products across Europe, the Middle East, and Africa, with a focus on clinical trial applications, marketing authorisation submissions, and lifecycle management. The professional will collaborate with cross-functional teams and regulatory agencies, ensuring compliance and timely approvals for oncology pharmaceuticals. Work includes drafting submissions, responding to health authority queries, and supporting scientific advice procedures.

Johnson & Johnson MedTech Poland PLN 121,000 – PLN 194,350 pa

Hybrid Permanent

Quality Engineer

As a Quality Engineer, you will lead quality initiatives in a manufacturing environment, ensuring the reliability and compliance of medical devices. You will apply statistical process control, conduct root cause analysis, and collaborate with cross-functional teams to drive continuous improvement and maintain quality standards.

Smith & Nephew Goole, United Kingdom

On-site Permanent

Technical Sourcing Program Manager

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the LifeThe...

Medtronic London, United Kingdom

R&D Engineer

As an R&D Engineer, you will work within a collaborative team to develop the next generation of medical devices, from early concept to clinical trials and manufacturing. Your role involves planning and delivering engineering work packages, translating user needs into engineering requirements, and working closely with cross-functional teams to ensure robust design outputs and regulatory compliance.

Smith & Nephew United Kingdom

Hybrid Permanent

EHS Specialist

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the LifeThe...

Medtronic Watford, United Kingdom

Mobile Service Technician - Medical Device Maintenance

This role involves on-site maintenance, calibration, and repair of advanced bio-decontamination systems in healthcare and cleanroom environments. Responsibilities include fault diagnosis, preventative maintenance, and customer training using ultrasonic vaporisation, hydrogen peroxide delivery, and embedded control systems.

Universal Business Team Bristol, Bristol (county), United Kingdom £35,000 – £40,000 pa

On-site Permanent

Mobile Service Technician - Medical Device Maintenance

This role involves maintaining and repairing advanced bio-decontamination and infection control equipment in healthcare and cleanroom environments. Responsibilities include preventative maintenance, fault diagnosis, calibration, and providing technical training to customers.

Universal Business Team Swindon, Wiltshire, United Kingdom £35,000 – £40,000 pa

On-site Permanent

Compliance Engineer (Medical Equipment)

The Compliance Engineer will oversee legislative compliance and product safety for medical equipment, ensuring all products meet relevant standards through rigorous testing and documentation. You will maintain a compliance database, participate in product design for certification, and conduct training to uphold compliance across the organization.

Ernest Gordon Recruitment Cheltenham, United Kingdom £55,000 pa

On-site Permanent

Quality Engineer (Compliance)

This role involves ensuring medical device and drug-device combination products meet strict regulatory and quality standards throughout development. The Quality Engineer will lead design controls and risk management activities, support audits, and ensure compliance with ISO and FDA regulations. They will work closely with development teams and external partners to maintain audit-ready documentation and contribute to regulatory submissions.

Next Phase Recruitment Cambridge, Cambridgeshire, United Kingdom

Hybrid Contract

Clinical Sales Support

This role involves providing clinical and sales support for medical technology products across the East Midlands, working directly with healthcare professionals to drive product adoption. The specialist will deliver training, clinical demonstrations, and expert guidance while ensuring regulatory compliance and gathering market insights. Collaboration with internal teams and maintaining strong stakeholder relationships are key to supporting customer success and improving patient care.

Robert Walters Derbyshire, United Kingdom £45,000 – £48,000 pa

Hybrid Permanent

Firmware Technical Lead - Medical Devices and Quality Systems

This role involves leading the firmware architecture and development for a life-sustaining wearable medical device. You will define the firmware architecture, development standards, and quality systems, ensuring alignment with IEC 62304, ISO 13485, and other regulatory standards. The position offers a unique opportunity to shape a greenfield project with a strong focus on patient safety and high-integrity engineering.

Verso Recruitment Teversham, Cambridgeshire, United Kingdom

On-site Permanent

Senior Quality Engineer

This role involves driving quality improvements within a medical device environment, focusing on quality planning, supplier oversight, and compliance with global regulatory standards. The Senior Quality Engineer will support new product introductions, lead validation activities, and manage non-conformances and CAPAs within an ISO 13485-certified QMS. The position operates in a hybrid model from the Innovation Centre in Bedford, working closely with contract manufacturers and regulatory teams.

Get Staffed Online Recruitment Bedford, United Kingdom £45,000 – £50,000 pa

Hybrid Permanent

Head of Engineering & Product Development

Leads end-to-end engineering and product development for complex electromechanical medical devices within a regulated environment. Responsible for overseeing R&D, NPI, and a critical in-flight next-generation product programme, ensuring compliance with ISO 13485 and UK/EU MDR standards. Works cross-functionally with quality, regulatory, manufacturing, and commercial teams to deliver innovative, compliant products from concept through to production and support.

CBSbutler Holdings Limited trading as CBSbutler Lancing, West Sussex, United Kingdom

On-site Permanent

Quality Engineer

The Quality Engineer will lead quality management system maintenance and improvement within a manufacturer of daily living aids, ensuring compliance with ISO 13485 and ISO 9001 standards. This role involves conducting root cause analyses, managing non-conformances, supporting regulatory submissions, and driving continuous improvement across manufacturing operations. The position works closely with production, regulatory, and HSE teams in a cross-functional environment.

Simpson Recruitment Services Hr81Aa, HR8 1AA, United Kingdom £38,000 – £43,000 pa

On-site Permanent