Latest Medical Services Jobs

Vulnerability Analyst - Product Security | /Freelance

A global medical device company is seeking a Vulnerability Analyst with experience in non-connected devices and known component threats to support on a 6-month contract basis.You'll support product security activity across medical device products already in the field. The role...

Real Limerick, Limerick County, Ireland £47 – £56 ph

Contract

Regulatory Affairs and Quality Assurance Assistant - Cambridge

Regulatory Affairs and Quality Assurance Assistant - Medical Devices - CambridgeDue to the growth of a medical devices company based in Cambridge, there is need for a new Regulatory Affairs and Quality Assurance Assistant to work with and support the...

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

Connectivity Specialist

Evolve are partnering with a driven medical device manufacturer who are seeking a Connectivity Specialist to help shape the future of connected healthcare. This is an exciting opportunity to combine technical expertise, customer engagement, and project leadership to deliver innovative...

Evolve Selection Newcastle upon Tyne, Tyne & Wear, NE1 4JA, United Kingdom

Connectivity Specialist

Evolve are partnering with a driven medical device manufacturer who are seeking a Connectivity Specialist to help shape the future of connected healthcare. This is an exciting opportunity to combine technical expertise, customer engagement, and project leadership to deliver innovative...

Evolve Selection Gloucester, Gloucestershire, United Kingdom

Connectivity Specialist

Evolve are partnering with a driven medical device manufacturer who are seeking a Connectivity Specialist to help shape the future of connected healthcare. This is an exciting opportunity to combine technical expertise, customer engagement, and project leadership to deliver innovative...

Evolve Selection Watford, Hertfordshire, United Kingdom

Regulatory Affairs Specialist

This role involves maintaining technical documentation and ensuring compliance with UK and EU MDR regulations for Class I and IIa medical devices. The specialist will support regulatory submissions, post-market surveillance, and quality management system development within a regulated environment. Collaboration with the QA Manager and ongoing product lifecycle support are key aspects of the position.

Cure Talent Upper Marlbrook, Worcestershire, B61 0RT, United Kingdom £45,000 – £50,000 pa

On-site Permanent

Regulatory Affairs Manager

Cure Talent are delighted to be partnered with a global medical device organisation recognised as one of the most established and successful healthcare companies in the world. With a diverse international footprint and a strong pipeline of innovation, the business...

Cure Talent Curbridge, Oxfordshire, Oxfordshire, United Kingdom £85,000 – £95,000 pa

Test Engineer

This role involves designing and implementing quality test procedures for both software and hardware components of medical devices. Responsibilities include attending design meetings, writing test plans, analyzing opportunities for automated testing, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa

On-site Permanent

Process Project Engineer – Moulding / Manufacturing

Process Project Engineer – Moulding / ManufacturingRoleExciting new role with our client a multinational Medical Device and Healthcare products provider. NIRAS is actively recruiting for an energetic and hands-on Manufacturing/Project Engineer to lead a key project within our Client’s Advanced...

NIRAS Ireland Castlebar, Mayo County, Ireland

Quality Engineer

This role involves leading the development and maintenance of a Quality Management System to ISO 134885 and ISO 9001 standards within a medical device manufacturer. The engineer will drive root cause analysis, manage non-conformance investigations, support regulatory compliance for global markets, and ensure quality in production and new product launches. It's a key role in a values-driven company focused on producing life-enhancing daily living aids.

Macstaff Ledbury, Herefordshire, United Kingdom £38,000 – £43,000 pa

On-site Permanent

Assembly Technician

Client;We are proud to be working alongside a truly ground-breaking medical device business, who are looking to appoint a process/assembly technician.POSITION; Process/Assembly TechnicianSHIFT; Monday - Friday 8 - 4:30Hourly Rate - £14.00 - £14.25 an hour.The key responsibilities for this...

Planet Recruitment Oxford, Oxfordshire, United Kingdom £14 – £14 ph

Test Quality Assurance Engineer

This role involves designing and implementing quality test procedures for both software and hardware in medical device products. Responsibilities include attending design meetings, writing test plans, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa

On-site Permanent

Regulatory Affairs Specialist

This role involves preparing and managing regulatory submissions for medical devices, ensuring compliance with EU MDR and ISO 13485 standards. The specialist will maintain technical documentation, support clinical evaluations, and collaborate with cross-functional teams throughout the product lifecycle. A key focus is staying current with global regulatory changes and ensuring continuous market access through timely renewals and post-market surveillance.

SRG Perivale, London, UB6 8DD, United Kingdom £50,000 – £60,000 pa

On-site Permanent

Embedded Software Engineer

This role involves designing and maintaining embedded C/C++ firmware for medical and mechatronic devices, taking full ownership of the software lifecycle, and establishing internal processes such as version control and documentation standards. The engineer will work hands-on with hardware teams, debug using test equipment, and lead the transition of firmware development from external contractors to in-house. It’s a rare opportunity to shape software engineering practices from the ground up within a small, mission-driven team focused on life-changing technology.

YT Technologies Belle Isle, West Yorkshire, WF1 5PS, United Kingdom £45,000 – £60,000 pa

Hybrid Permanent

Director, Clinical Trial and Data Transparency

This role involves providing strategic and operational expertise for the disclosure of clinical regulatory documents on public websites, ensuring compliance with global regulatory requirements. Responsibilities include managing disclosure activities, overseeing vendors, and developing standard processes and technologic solutions to support transparency in clinical trials.

Pfizer India

Remote Permanent