Latest Regulatory Affairs Specialist Jobs

Medical Safety Officer - PALM

This role involves leading the safety assessment and risk management of pharmaceutical products across their lifecycle, with a focus on evaluating safety data from clinical trials, literature, and post-market sources. The Medical Safety Officer provides medical expertise to cross-functional teams, contributes to regulatory submissions, and ensures compliance with global pharmacovigilance standards. A key responsibility is leading Safety Management Teams and guiding risk mitigation strategies in collaboration with regulatory authorities and internal stakeholders.

Johnson & Johnson MedTech

Regulatory Affairs - Student Placement 2027

This role involves hands-on experience in Regulatory Affairs, supporting worldwide product registration and compliance activities. You will collaborate with global teams, maintain regulatory databases, and gain exposure to different markets and regulatory environments.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Internship

Service Engineer

This role involves maintaining and repairing medical decontamination equipment, including sterilizers, washer disinfectors, and endoscopes. The engineer will perform diagnostic repairs on electrical, mechanical, pneumatic, and plumbing systems across healthcare facilities. The position requires strong technical troubleshooting, regulatory compliance awareness, and independent fieldwork across the Bristol region.

Ascend Consulting Bristol, Bristol (county), United Kingdom £35,000 – £48,000 pa

Biomedical Field Service Engineer

This role involves performing preventative maintenance and repairs on medical equipment in UK hospitals, ensuring minimal disruption to hospital operations. You will work closely with the site manager, maintain service documentation, and interact with customers and OEM staff, requiring strong communication and technical skills.

Focus Resourcing United Kingdom

On-site Permanent

Compliance Officer

This role involves leading product regulatory compliance for a portfolio of chemical and healthcare products, with responsibilities including monitoring regulations, preparing Safety Data Sheets, and supporting product registrations in the UK and Europe. The Compliance Officer will act as the main contact for external regulators, deliver internal training, and ensure compliance across product development and marketing. The position requires a scientific background and experience with chemical regulations such as REACH and CLP.

Reed Sg12Fs, United Kingdom £45,000 – £55,000 pa

Hybrid Permanent

Senior Quality Engineer

This role involves owning and improving the Quality Management System (QMS) within a medical device manufacturer, ensuring compliance with ISO 13485, EU MDR, and FDA regulations. The engineer will lead QMS processes including deviation management, CAPA, document control, and internal audits, while collaborating with operations, regulatory, and supply chain teams. Key responsibilities include supplier audits, root cause analysis, and driving continuous quality improvements in a highly regulated environment.

Walker Cole International Leeds, West Yorkshire, United Kingdom

Senior Embedded Software Engineer

This role involves leading embedded software development for medical devices used in critical care environments. The engineer will define software architecture, ensure regulatory compliance, and collaborate with cross-functional teams to deliver high-reliability systems. It offers the chance to work on life-saving technology with significant technical and clinical impact.

KO2 Embedded Recruitment Solutions Halton, Cheshire, United Kingdom £60,000 – £70,000 pa

Hybrid Permanent

Scientific Equipment Technician

As a Scientific Equipment Technician, you will maintain and troubleshoot a wide range of laboratory equipment, ensuring it operates efficiently and complies with regulatory standards. You'll work closely with scientists and laboratory teams to resolve technical issues, manage spare parts, and contribute to process improvements across two sites.

Broughton Group Bb186Jz, United Kingdom £27,297 – £30,500 pa

Quality Technician

Quality Technician, £28,000 - £32,000, Abingdon, Oxfordshire• £28,000 - £32,000 depending on experience + pension + 25 days holiday• Full-time, permanent position• Quality-focused role within a growing medical device manufacturing company operating to ISO 13485Are you a detail-driven Quality Technician...

Euro Projects Recruitment Abingdon, OX14 5BH, United Kingdom

Windows Software Manager

The Windows Software Manager leads the design and development of Windows-based software for medical devices, ensuring robust solutions in regulated environments. Responsibilities include team management, project planning, technical oversight, and compliance with regulatory standards.

OrganOx Oxford, United Kingdom

On-site Permanent

Backend Developer

Design and develop scalable backend services, APIs, and cloud-native solutions on Microsoft Azure to support OrganOx's medical device platforms. Work with regulated software processes, build automated DevOps pipelines, and ensure secure, high-quality delivery of systems that impact clinical outcomes. Collaborate with internal and external teams to refine requirements and maintain robust technical documentation.

OrganOx Oxford, United Kingdom

On-site Permanent

Senior Software Engineer

Develop and maintain high-performance embedded software for next-generation intra-operative medical devices using modern C++ and edge computing technologies. Collaborate across multidisciplinary teams to enhance device connectivity, real-time decision support, and cloud integration within a regulated medical environment. Focus on code quality, security, and reliability in a system-critical context.

Medtronic London, United Kingdom £76,800 – £115,200 pa

Hybrid Permanent

Service Activation Manager, Integrated Health Solutions

Leads complex healthcare supply chain managed service projects for Operating Room and Cath Lab solutions, from initiation through implementation and stabilization. Coordinates cross-functional teams, manages project risks and change requests, and ensures delivery within scope, timeline, budget, and quality standards while maintaining strong customer relationships and regulatory compliance.

Medtronic Watford, United Kingdom £86,160 – £129,240 pa

Global Supply Planning Manager (9-12-month fixed-term

The Global Supply Planning Manager will lead a team of global master planners to create and execute an optimized end-to-end supply plan, ensuring balance between service, inventory, and cost. They will use SAP and Kinaxis Maestro to drive supply planning activities, collaborate with cross-functional teams, and continuously improve supply chain processes.

Smith & Nephew United Kingdom

Contract

Field Service Engineer - South East

Install, maintain, and repair advanced MRI systems across the South East of England, ensuring optimal performance and minimal downtime. Diagnose complex mechanical, electrical, and software issues while maintaining compliance with quality and safety standards. Build strong customer relationships and contribute to continuous service improvement within a regulated healthcare environment.

Philips United Kingdom

Remote Permanent Clearance Required