Latest product manager Jobs

Field Service Engineer, Medical Diagnostic Systems

This role involves on-site service and repair of advanced medical diagnostic systems used in NHS and private laboratories. The engineer will troubleshoot technical issues, perform maintenance, and deliver customer support across pathology and clinical chemistry environments. Full product training is provided, and the role requires a flexible schedule including weekend work.

TRS Consulting Plymouth, Devon, United Kingdom £52,000 pa

Field Service Engineer, Medical Diagnostic Systems

Perform installation, maintenance, and repair of advanced medical diagnostic systems in NHS and private laboratory settings. Provide on-site technical support and troubleshooting for complex equipment. Role includes extensive customer interaction and requires adaptability to occasional weekend work.

TRS Consulting Stirling, Stirling And Falkirk, United Kingdom £52,000 pa

Lead, Trial Delivery Management

This role involves leading the execution of clinical trial activities at the study level, including managing trial-specific documentation, vendor oversight, and regional coordination. The individual will support compound training, contribute to operational strategies, and ensure compliance with regulatory standards across global trials. Key responsibilities include risk mitigation, process improvement, and mentoring team members within a matrixed, global environment.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Lead, Trial Delivery Management

This role involves leading the execution of clinical trial activities, including creating trial-specific documentation, managing vendor relationships, overseeing regional trial delivery, and supporting compound training. The position requires managing operational strategies, mitigating risks, and ensuring compliance across global clinical trials. It also includes mentoring team members and contributing to process improvements within a matrixed, global environment.

Johnson & Johnson MedTech Netherlands €64,000 – €103,040 pa

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

Process Technology Engineer

This role involves optimizing manufacturing and packaging processes, leading technical projects to improve efficiency and safety, and supporting the implementation of new technologies in a production environment. The engineer will work closely with cross-functional teams to enhance operational performance, manage capital projects, and ensure process standardization. Emphasis is placed on continuous improvement, safety culture, and technology transfer across global operations.

ADM Somerset, United Kingdom

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 Design Assurance Engineer

This role involves ensuring medical device designs comply with global regulatory standards throughout the product development lifecycle. You'll lead design assurance activities including risk management, design controls, and verification/validation, working closely with engineering and quality teams. The position emphasizes compliance with ISO 13485, ISO 14971, and 21 CFR Part 820 within a highly regulated environment.

SRG Cambridge, Cambridgeshire, United Kingdom £60,000 – £70,000 pa

Senior Quality Associate

This role involves overseeing key quality assurance processes such as NCR, CAPA, and change control within a medical device development environment. The individual will ensure compliance with regulatory standards, support audit readiness, lead training initiatives, and drive continuous improvement across QA systems. Emphasis is placed on data integrity, cross-functional collaboration, and maintaining robust documentation for design history and regulatory submissions.

Adepto Technical Recruitment Ltd Cambridge, Cambridgeshire, United Kingdom £40,000 – £50,000 pa

On-site Permanent

Medical Device Development Engineer

Design and develop innovative medical devices from concept to manufacture, working across the full product development lifecycle. Perform CAD design, prototyping, testing, and support verification and validation in a quality-focused, regulated environment. Collaborate with multidisciplinary teams to translate clinical requirements into reliable, manufacturable solutions.

Euro Projects Recruitment Shippon, Oxfordshire, United Kingdom £38,000 – £42,000 pa

NPI Engineer

The NPI Engineer will lead the industrialisation and technology transfer of medical devices from development into controlled manufacturing, ensuring robust, validated processes in compliance with ISO 13485. This role involves cross-functional coordination, process development, equipment specification, and creating manufacturing documentation to bridge design and production. The position offers ownership of end-to-end NPI projects within a growing, innovative medical device company.

Euro Projects Recruitment Shippon, Oxfordshire, United Kingdom £40,000 – £45,000 pa

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

Preclinical In-Vitro Toxicology Scientist

This role involves leading and executing in-vitro toxicology studies, including Neutral Red, Ames, and micronucleus assays, within a regulated laboratory environment. The scientist will develop and optimise testing methodologies, interpret complex biological data, and support regulatory submissions. They will work collaboratively across multidisciplinary teams and with external partners to advance pre-clinical testing capabilities in product safety assessment.

Hudson Shribman United Kingdom £55,000 – £70,000 pa

Design Engineer

This role involves designing and developing injection-moulded products from concept to manufacturing, with a focus on innovation and regulatory compliance. The engineer will create prototypes, validate designs, and collaborate with global teams, particularly in Asia and the US. Work centres on medical or high-regulation applications requiring precision and adherence to quality standards.

Reed Sy164Le, United Kingdom £40,000 – £45,000 pa

Hybrid Permanent

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