3 weeks ago Be among the first 25 applicants Lead the evolution of a breakthrough medical device into large-scale real-world use. Neupulse has developed a breakthrough neuromodulation medical device that helps people with Touret...Read More>>.

No7 Beauty Company, part of Boots in Nottingham, is seeking a Regulatory Manager to lead regulatory strategies in product development. You will manage a team of experts to ensure compliance with industry standards while driving successful product...Read More>>.

AbbVie is seeking an experienced professional to lead International Regulatory Advertising and Promotion within Allergan Aesthetics. The role requires oversight of global guidelines, collaboration with Commercial, Medical, Legal and Compliance tea...Read More>>.

Medical Device Regulatory and Quality Consultant We are seeking a highly skilled consultant with experience in medical device and/or combination product Quality and Regulatory processes to join our Healthcare & Life Sciences (HLS) cons...Read More>>.

ECM Selection (Holdings) Limited in Cambridge seeks an engineering leader to guide high-value development programmes from concept through transfer to manufacture. You will accelerate timelines, manage risk, and deliver results that improve patient...Read More>>.

GB69 (FCRS = GB069) Sandoz Ltd. is seeking a skilled professional to lead project management in the medical device field in Cambridge, England. You will be responsible for overseeing design processes and ensuring compliance with ISO standards....Read More>>.

Senior Risk Management Engineer, Medical Devices (ISO 14971/ IEC 60601/IEC 62304) Vision RT is a rapidly growing MedTech which is transforming radiation therapy for cancer patients, helping to make it more accurate, effective and comfo...Read More>>.

binx health seeks a Senior Electromechanical Engineer to join our teams delivering FDA-regulated medical devices that provide clear, actionable diagnostic results. You will design, test, and refine electromechanical equipment and work with enginee...Read More>>.

CMR Surgical is seeking a senior electronics contractor in the UK to join the Versius Plus Ultimate program. You will work with the electronics team to interpret requirements, capture schematics in Altium, and support PCB layout and test in the sy...Read More>>.

PROCEPT BioRobotics UK, Limited in the United Kingdom is seeking a field-based Sales Manager to launch Aquabeam and establish Aquablation as the treatment of choice for BPH. You will maximize utilization of installed systems and collaborate with c...Read More>>.

Vitalograph is seeking an experienced Global Product Manager to lead the comPAS PFT Solutions portfolio, spanning software and hardware. Reporting to the EVP comPAS PFT Solutions, you will champion the portfolio, aligning user needs, clinical insi...Read More>>.

Freelance Director of Regulatory Affairs - Cosmetics (U.S. & EU)Join to apply for the Freelance Director of Regulatory Affairs - Cosmetics (U.S. & EU) role at Coronado ResearchFreelance Director o...Read More>>.

Overview Territory Sales Manager – Dental & Medical Devices Location: Manchester, Cheshire, Merseyside, Lancashire Salary: £50–70K package (competitive basic + uncapped commission, bonuses, and b...Read More>>.

This role will be leading the QA and QC teams at the manufacturing site, as well as maintaining QMS systems and licensingOur client is a well-established medical device business, with a large manufacturing site based in Nottingham. They...Read More>>.

Regulatory Connect in the United Kingdom seeks an experienced EU Regulatory Affairs Director to shape strategy and lead delivery across diverse development programmes from early assets to MAAs.You will enjoy client interaction, take ownersh...Read More>>.

Alnylam Pharmaceuticals (Nasdaq: ALNY) seeks a Senior Manager, Regulatory Affairs to partner with EU and global regulatory leads and cross-functional teams to plan and deliver regulatory submissions across the product life cycle.You will de...Read More>>.

R&D Partners in the United Kingdom is seeking a Regulatory Affairs Manager to lead a team of regulatory experts and drive strategic initiatives for cosmetics and OTC products. You will shape regulatory strategy, oversee product development complia...Read More>>.

Energy Jobline ZR seeks a Senior Mechanical Engineer in Cambridge to drive design from early concepts through high‑volume manufacture for next‑generation medical devices. You will work within a multidisciplinary team to develop precision mecha...Read More>>.

GBUK is seeking a Head of Regulatory Affairs and Quality Affairs to lead the Quality Management System across our UK and Ireland sites. The role focuses on ISO 13485 and ISO 9001, regulatory oversight of suppliers, labeling, and field activities,...Read More>>.

Ofcom in Edinburgh seeks a Senior Associate to lead Scotland affairs across telecoms, spectrum, and consumer policy. You will build relationships with government, Parliament, and industry, and guide regulatory thinking with a Scotland-focused lens...Read More>>.

Closing Date: 26/10/2026 Group: Strategy and Research Group Management Level: Senior Associate Job Type: Permanent Job Description: Please note that this role will close at 00:01 on Monday 26 October, and therefore we advise getting your applicati...Read More>>.

Cure Talent are delighted to be partnered with a growing medical device certification organisation that is expanding its scope into a number of additional medical device technologies. As part of this expansion, we are looking to speak with...Read More>>.

The RoleJoining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. Moderna is strengthening its presence in Lond...Read More>>.

JOB DESCRIPTION: About the Role We are seeking an experienced and results-driven Manager, Medical Devices Service Centre to lead a critical service operation supporting our medical device portfolio. This role is responsible for delivering exceptio...Read More>>.

Zenovo is seeking an Embedded Software Engineer in Cambridge to develop software for medical devices. You will work on real-time control, sensor data handling and hardware integration in a collaborative engineering environment.The role focu...Read More>>.

ARCA Consulting Ltd seeks an experienced Mechanical Engineering Manager for Medical Devices to lead cross-disciplinary product development programs. You will own technical direction, delivery, budgets and schedules while guiding mechanical, electr...Read More>>.

Consult is seeking a senior Cybersecurity Regulatory Affairs Consultant for a fully remote contract with a UK medical device company. The role focuses on software and cybersecurity regulatory submissions and documentation.You will work auto...Read More>>.

Senior/Principal Optical Engineer – Medical Device & Imaging Systems 7 Jul 2026 Location: Oxford Type: Permanent, Full-time Background Pictura Bio is an innovative MedTech start-up developi...Read More>>.

Abbott Diabetes Care in the United Kingdom seeks a Senior Manager of Design Transfer to oversee the transfer of glucose monitoring products from R&D into manufacturing. You will collaborate with Quality, Operations, Engineering, Regulatory Affairs...Read More>>.

Senior Manager, Regulatory Submission Locations: King of Prussia, PA | Glattburgg, Switzerland | Maidenhead, UKWork Arrangement: Hybrid - 3 days onsiteReports to: Global Submission Management Lead CSL...Read More>>.

Maclivaro Limited is seeking an experienced Operations Manager to lead manufacturing, warehousing, supply chain and QA at our Houghton Regis site. You will drive performance, optimise processes and contribute to the longer-term strategic plan....Read More>>.

Gold Group is seeking an Electrical Engineer for medical devices in Cornwall. You will design electrical systems, develop schematics and PCBs, verify and validate devices, and ensure EMC/safety compliance while collaborating with global R&D teams....Read More>>.

Bluetree Recruits is seeking a Senior Regulatory Affairs & Quality Manager in Cambridge to shape regulatory strategy for the US first and expand globally. You will own FDA, CE and UKCA submissions and lead a robust QMS, partnering with leadership...Read More>>.