Overview Join Moody’s Government, Public and Regulatory Affairs to guide insurance regulatory strategy across EMEA. You will shape policy positions, engage with regulators, and apply AI-driven approaches to improve regulatory workflows. T...Read More>>.

Overview In this role you will design and develop electronics for cutting-edge medical devices, contributing to life-saving technologies. You will join a dedicated medical devices team on-site in Cambridgeshire, tackling complex design chal...Read More>>.

Overview In this role you ensure quality across medical device projects in a growing Cambridge-based team. You will focus on quality assurance under ISO 13485, with advantageous knowledge of EN 60601, and contribute to technical files and t...Read More>>.

Overview In this role, you will assess and improve quality management systems for software-based medical devices, ensuring regulatory compliance and robust processes. You’ll work within a cross-functional context to strengthen QMS and sup...Read More>>.

Overview In this role you act as Ofcom’s lead contact for Scotland across consumer, telecoms, spectrum and postal duties. You will build relationships with senior government, Parliament, and industry stakeholders, and coordinate cross-tea...Read More>>.

Overview In this role you will lead cutting-edge development projects within a multidisciplinary medical devices team in Cambridge, driving from concept to commercialization. You will oversee cross-functional groups, ensuring timelines and...Read More>>.

Overview In this role you will help invent and improve Medical Devices within a collaborative, multi-disciplinary environment in Cambridge. You’ll translate inventive ideas into practical devices across drug delivery, diagnostics, wearabl...Read More>>.

Overview In this role you contribute to the design and development of cutting-edge medical devices, working within a multidisciplinary design team to deliver safe, reliable products. You will join a growing part of the business with clear c...Read More>>.

Overview In this role you will lead international CMC regulatory activities to support global product development. You’ll manage agency communications, ensure quality CMC sections, and influence submissions across multiple programs. You w...Read More>>.

Overview In this role, you shape and execute the Global Regulatory Affairs strategy for the IVD and life sciences portfolio, guiding regulatory pathways and milestones across the product lifecycle. You will lead regulatory submissions with...Read More>>.

Overview In this role, you will collaborate with engineers and scientists in Cambridge to invent and advance new medical devices. You work across multiple projects, solving complex problems while keeping pace with evolving Technologies and...Read More>>.

Overview In this role you will lead the development and execution of global regulatory strategies for international markets, shaping regulatory input across multiple programs. You will collaborate with regional teams to align clinical and c...Read More>>.

Overview In this role you contribute to EU regulatory strategies for Amgen’s biosimilar portfolio, guiding submissions from development to launch and lifecycle management. You will collaborate with global and regional teams to prepare MAA...Read More>>.

Overview In this role you will support Moody's Government, Public and Regulatory Affairs strategy for the EMEA region, engaging with regulators, governments and industry groups. You will help expand insurance regulatory coverage, prepare st...Read More>>.

Overview In this role you will contribute to inventing and developing brand-new medical devices in a fast-growing setting in London. You will collaborate with physicists, mechanical engineers, and scientists to create lifesaving technologie...Read More>>.

Overview As a Senior Electronics Engineer, you will lead electronic design activities for medical devices that meet ISO 13485 standards and help take products to market. You will work within a cross-functional team of engineers and scientis...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>>.

About AbbVieAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives a...Read More>>.

Do you want to contribute to a safer market while gaining an authentic international experience as a consultant? Obelis is currently looking for a RA Expert Consultant specialized in food supplements! Your role will be:...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>>.

Senior Mechatronics Engineer - Cambridge - Medical DevicesA leading medical devices organisation in Cambridge is expanding its development team and is seeking a highly capable Senior Mechatronics Engineer to drive the creation of new,...Read More>>.

Senior Mechatronics Engineer - Cambridge - Medical DevicesA leading medical devices organisation in Cambridge is expanding its development team and is seeking a highly capable Senior Mechatronics Engineer to drive the creation of new, li...Read More>>.

Newton Colmore Consulting seeks a Senior Mechatronics Engineer in Cambridge to drive multi‑disciplinary medical device development. You will design, prototype and test devices, collaborating with mechanical, electronics and physics experts to de...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>>.

Newton Colmore is seeking a Senior Mechatronics Engineer in Cambridge to drive the creation of life‑changing medical devices. You will work hands‑on with a multidisciplinary team to design, prototype and refine complex devices across several s...Read More>>.

eg technology is seeking a seasoned Project Manager to lead planning, control and delivery of complex product design and development projects from concept to manufacture. You’ll work with clients and motivate multidisciplinary teams across softw...Read More>>.

Regulatory Affairs Specialist (Food Ingredients) Recruiter @ Seven Search and Selection Ltd | Specialising in Retail & FMCG Our client: A global leader in ingredient solutions, supporting innovation across fo...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>>.

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>>.

CMR Surgical Ltd. in Cambridge is seeking a Software Engineer for the Robot Software team. You will develop embedded software for CMR medical devices, mainly in C, and contribute to regulatory compliant test coverage and tooling.You will jo...Read More>>.

AbbVie seeks an experienced International Regulatory Affairs professional to provide position and guidance on advertising and promotion. You will collaborate with Commercial, Medical, Legal, and Compliance teams to ensure compliant, effective comm...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>>.

OrganOx Limited is seeking a Senior IP Specialist to define and execute the company’s global IP strategy. The role acts as the internal authority on IP matters and collaborates with R&D, regulatory, and business teams to protect and exploit the...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>>.

CV TECHNICAL LTD is seeking a Senior Automation Engineer in Dorset to lead automated assembly projects from concept through commissioning, validation and full production implementation. You will collaborate with Operations, Quality, R&D, Validatio...Read More>>.