Latest Medical Services Jobs

Sr. Source Reg Compliance Specialist

The Sr. Source Regulatory Compliance Specialist is responsible for ensuring suppliers and externally provided processes comply with regulatory requirements and quality standards. Key responsibilities include executing supplier audits, supporting compliance oversight, and maintaining documentation. The role involves close collaboration with Quality, Regulatory Affairs, Supply Chain, and Procurement teams to maintain product quality and supply continuity.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

Specialist Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. They actively participate in risk management activities, maintain clinical quality plans, and communicate risk updates to stakeholders through regular review cycles.

Johnson & Johnson MedTech United States

On-site Permanent

Principal Clinical Research Specialist

The Principal Clinical Research Specialist will lead and manage multi-site clinical studies for Pelvic Health across Europe, ensuring compliance with regulations and delivering high-quality clinical evidence. Responsibilities include designing study protocols, overseeing trial operations, and collaborating with investigators and cross-functional teams.

Medtronic Watford, United Kingdom £64,800 – £97,200 pa

Remote Permanent

Sales Representative

The Sales Representative role involves developing and maintaining Medtronic's Embolisation, Deep Venous, and Peripheral Vascular portfolios with existing and new customers. Responsibilities include analyzing the marketplace, building sales strategies, and providing technical and clinical support to healthcare professionals.

Medtronic London, United Kingdom £43,200 – £64,800 pa

On-site Permanent

Marketing Manager (RENASYS)

Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.Are you driven by the opportunity to help shape global marketing strategy in a fast moving, innovation led environment? This is a chance to play a...

Smith & Nephew Watford, United Kingdom

Operational Quality 1

The Operational Quality 1 role involves maintaining high standards of quality and compliance in the manufacturing process. Responsibilities include reviewing and releasing product documentation, managing non-conformances, and supporting quality audits. The role also involves leading investigations and dispositions of defective materials and ensuring compliance with quality management systems.

Smith & Nephew Goole, United Kingdom

Hybrid Permanent

Director, PMO

The Director of PMO will lead the creation and maturation of OrganOx’s central Project Management Office, establishing frameworks, governance, and a project-oriented culture. Key responsibilities include strategic leadership, team development, and ensuring alignment with enterprise goals to drive successful project outcomes and sustainable growth.

OrganOx Oxford, United Kingdom

On-site Permanent

Head of Research and Development

We’re partnering with a market-leader in the Ophthalmology sector, who are looking to recruit an experienced Head of R&D (Research & Development)!The successful candidate will lead R&D strategy, manage a multidisciplinary team, and work closely with key internal functions to...

Evolve Selection Cambridge, Cambridgeshire, United Kingdom

Remote Permanent

Mechanical Engineer

This role involves taking ownership of mechanical engineering aspects for key project subsystems and new technology developments. You will collaborate with multi-disciplinary teams, uphold best-practice design standards, and ensure compliance with international regulations in a high-tech manufacturing environment.

Randstad Engineering Bristol, Bristol (county), United Kingdom £44,000 pa

Hybrid Permanent

Metrology Applications Engineer

This role involves conducting precision measurements, preparing inspection reports, and supporting the sales team with technical demonstrations and customer applications. You will also install metrology systems, train operators, and provide technical support to customers and distributors, both in the UK and internationally.

Syntech Recruitment Woking, Surrey, United Kingdom £55,000 – £60,000 pa

On-site Permanent

Clinical Trials Associate

The Clinical Trials Associate will manage Trial Master File (TMF) activities, ensure regulatory compliance, and support the delivery of clinical studies. Responsibilities include maintaining TMF, coordinating documentation, and assisting with site visits and data management.

SRG Hitchin, Hertfordshire, SG5 1HP, United Kingdom

On-site Permanent

Quality Engineer

The Quality Engineer will manage product quality issues, implement corrective actions, and lead problem-solving sessions using tools like 8D, 5 Whys, and Fishbone Diagrams. They will collaborate with cross-functional teams to enhance product quality, optimize processes, and support new product introductions.

Azenta Life Sciences Wotton, Surrey, Surrey, United Kingdom

On-site Permanent

Development & Regulatory Chemist

This role involves developing and validating analytical methods for APIs, authoring and maintaining ASMFs, and supporting regulatory submissions. The chemist will work closely with cross-functional teams to ensure high-quality documentation and compliance with ICH and GMP standards.

SRG Hitchin, Hertfordshire, SG5 1HP, United Kingdom

On-site Permanent

Senior Clinical Application Specialist - MCS

This role involves driving the adoption of advanced clinical applications in microsurgery and tumour workflows, working closely with surgeons, clinical teams, and hospital decision-makers. Key responsibilities include supporting technology integration, engaging key opinion leaders, and contributing to strategic business development.

Manpower Manchester, United Kingdom

Hybrid Permanent

Pharmaceutical Quality Engineer

The role involves providing quality engineering support across manufacturing, validation, and supply chain operations, ensuring compliance with GMP and GDP standards. Key responsibilities include leading deviation investigations, managing CAPA processes, and supporting internal and external audits. The position also focuses on continuous improvement and collaboration with cross-functional teams.

Smart4Sciences Cheshire, United Kingdom

On-site Contract Flexible