Latest Medical Devices Jobs

Service Program Manager

As a Service Program Manager at Medtronic, you will lead and manage complex projects and programs across the Digital Technologies Business Unit, focusing on business process improvement and the development of service-wide systems. You will work closely with cross-functional teams to enhance service delivery, develop global service strategies, and drive customer satisfaction through effective communication and project management.

Medtronic London, 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

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 United Kingdom

Sales Specialist |Johnson & Johnson MedTech | Orthopedics| Cambridge & Norwich

This role involves driving sales of orthopedic medical devices within a defined territory, focusing on building relationships with surgeons and healthcare professionals in secondary care. The specialist will develop account strategies, deliver product training, and promote new technologies through consultative selling. Clinical expertise and collaboration with internal teams are essential to support customer needs and grow market share.

Johnson & Johnson MedTech United Kingdom

Hybrid Permanent

Senior QC Analyst

This role involves leading and conducting analytical testing of raw materials, intermediates, and finished products within a GMP-regulated laboratory. The Senior QC Analyst ensures data integrity in line with ALCOA+ principles, investigates deviations and out-of-specification results, and mentors junior team members. The position emphasizes compliance, accurate documentation, and continuous improvement in a highly regulated pharmaceutical environment.

Smart4Sciences Netherlands, United Kingdom £10,000 – £11,000 pa

On-site Permanent

Quality Systems PMO Program Manager

This role involves leading the management and execution of global Quality Management System (QMS) transformation and harmonisation projects. Responsibilities include program governance, QMS integration, risk management, and continuous improvement initiatives to ensure compliance and operational excellence across a global network of divisions and sites.

Randstad Engineering Basingstoke, Hampshire, United Kingdom £27 ph

Hybrid Contract

Quality and Regulatory Labelling Program Manager

This role involves leading global labelling initiatives to ensure compliance with regulatory standards across various markets. The Program Manager will collaborate with cross-functional teams to manage change controls, mitigate risks, and drive continuous improvement in labelling processes.

Randstad Engineering Popley, Hampshire, RG24 9TW, United Kingdom £27 ph

Hybrid Contract

Quality Lead

This role involves leading quality and regulatory compliance for a multinational manufacturer across Europe and Africa, with a focus on medical devices and consumer products. The candidate will oversee the Quality Management System, lead audits, support new product launches, and drive continuous improvement through data analysis and cross-functional collaboration. It requires deep expertise in standards like MDD/MDR, ISO 13485, and QSR, along with strong leadership in technical quality environments.

New Appointments Group Folkestone, Kent, United Kingdom

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

Head of Quality Assurance and Regulatory Affairs

Evolve are partnering with a fast-growing organisation to appoint a Head of Quality Assurance & Regulatory Affairs. This is a strategic leadership role where you will drive quality and regulatory excellence, support global expansion, and work cross-functionally to ensure consistently...

Evolve Selection London, United Kingdom

Automation Engineer - Pharmaceutical

This role involves maintaining and troubleshooting automation and control systems in a GMP-regulated pharmaceutical manufacturing environment. You will participate in computerized system validation, support continuous improvement projects, and collaborate with cross-functional teams to ensure compliance and data integrity.

Smart4Sciences West Yorkshire, United Kingdom

On-site Permanent

Clinical Specialist Joints East Anglia & surrounds | Johnson & Johnson MedTech | Orthopedics

The Clinical Specialist Joints role involves providing in-theatre support to consultants and nursing staff, ensuring accurate information and training on orthopaedic products, and maintaining seamless supply and service to customers. This position is part of Johnson & Johnson MedTech's DePuy Synthes team, focusing on sales and customer support in East Anglia and surrounding areas.

Johnson & Johnson MedTech Peterborough, PE1 1XH, United Kingdom

On-site Permanent

Analytical Chemist

The role involves conducting and documenting analytical testing of pMDIs using HPLC and other techniques, ensuring data quality, and representing the department professionally. The position offers opportunities for continuous improvement and working in a GMP environment.

SRG Loughborough, Leicestershire, LE11 2QG, United Kingdom

On-site Temporary

Quality Manager

This role involves overseeing quality control processes on the manufacturing floor for electronic equipment, ensuring compliance with internal and regulatory standards. The Quality Manager will lead root-cause analysis, implement corrective actions, and work closely with engineering teams to transition products from prototype to production. Key responsibilities include maintaining SPC systems, driving continuous improvement, and ensuring adherence to ISO 9001 and IPC standards.

Advanced Technical Recruitment Nottingham, Nottinghamshire, United Kingdom

On-site Permanent

Quality Control Release Specialist 2

This role involves ensuring compliance with regulatory requirements and company procedures for the release of manufactured medical products. Responsibilities include leading the coordination and training of QC Release personnel, managing quality processes, and supporting continuous improvement initiatives.

Smith & Nephew Goole, United Kingdom

On-site Permanent