Test Technician - Medical & Drug Delivery Devices Permanent | On-site Location: Great Chesterford area, Cambridgeshire - up to £28,000Are you looking to start or build your career in medical device testing? We're hiring a...Read More>>.

Overview As Director, Regulatory Affairs, Labelling you will lead global labelling strategy for Ipsen’s products across development and lifecycle management. You will shape early labeling input with development teams and ensure USPI, EU l...Read More>>.

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 lead Voy’s Government & Regulatory Affairs to shape policy, engage regulators and policymakers, and translate business priorities into actionable workstreams. You’ll build proactive relationships with bodi...Read More>>.

Overview In this role you will help invent life-changing medical devices from Cambridge, collaborating with physicists, engineers and industry experts. You’ll work across imaging, surgical systems, electro-medical and other complex techno...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 lead drug delivery and combination product programmes from concept to industrialisation within PA’s life sciences practice. You provide senior technical leadership across engineering, usability, risk and manufact...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 remote, contract-based role you lead global regulatory strategy and submissions for oncology development programs. You will serve as Global Regulatory Lead, guiding cross-functional teams and aligning with corporate objecti...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 As Senior Manager, Regulatory Affairs at Alnylam, you will drive EU and global regulatory submissions for RNAi therapeutics, collaborating with EU/regulatory leads and cross-functional teams to shape strategy and submissions across...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>>.

Quality Assurance Regulatory Affairs Manager Strong training, communications, project management skills. Experience in Project management tools & systems. Proven successful experience on the design and development of trai...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>>.

Join to apply for the Associate Director, Regulatory Affairs role at KalVista Pharmaceuticals, Inc. 1 day ago Be among the first 25 applicants About KalVista Pharmaceuticals, Inc. KalVista is a global pharma...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>>.

Model: 2-3 days a week in the London office Duration: 6 months contract INSIDE IR35 (view to extend) Must have experience with horizon scanning and regulatory watch. Job Purpose Provide interim...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>>.

1 week ago Be among the first 25 applicantsGet AI-powered advice on this job and more exclusive features.Direct message the job poster from Entrust Resource SolutionsFinding Outstanding Talent in the Emerging Scientific Indus...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>>.

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>>.

Moderna is seeking an experienced CMC Regulatory Affairs professional to lead global CMC strategies and oversight for international submissions in London. The role requires coordinating regulatory filings, ensuring health authority compliance, and...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>>.

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>>.