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 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 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 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 you will shape and execute global regulatory strategy for a late-stage biotech program. You will work closely with senior stakeholders and external partners to navigate major markets, including...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 EU Regulatory Affairs Manager role, you help secure and maintain EU licenses for clinical trials and marketed products, supporting one or more products from an EU regulatory perspective. You may lead regulatory activities f...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>>.

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>>.

Cure Talent are delighted to be partnered with a global medical device company recognised for its life-saving technologies. As they continue to expand their portfolio, we have an opportunity for a Senior Regulatory Affairs Specialist to join th...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>>.

Arevna Cambridge, England, United KingdomRegulatory Affairs Manager (IVD)Arevna Cambridge, England, United Kingdom2 days ago Be among the first 25 applicantsDirect message the job poster from ArevnaOverview...Read More>>.

Position Position: Quality Assurance & Regulatory Affairs Manager / Director Location: Middlesex, West London, Surrey Please note: You MUST be able to work in the office 5 days per we...Read More>>.

Join Eye2Gene as our Quality and Regulatory Affairs Manager (SaMD/ AIaMD) Applicants must already have the right to work in the UK. Eye2Gene is a VC-funded, AI-powered precision ophthalmology platform combining imagi...Read More>>.

Select Pharma Limited provided pay rangeThis range is provided by Select Pharma Limited. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay rangeDirect messa...Read More>>.

Select Pharma Recruitment provided pay range This range is provided by Select Pharma Recruitment. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range Di...Read More>>.

BTG Pharmaceuticals, now SERB Pharmaceuticals, is looking for a Regulatory Affairs professional to manage submissions to Regulatory Authorities. The role requires a strong background in pharmaceuticals, particularly with regulations from MHRA, EMA...Read More>>.

Responsible for developing and managing the company's compliance framework for e-cigarette and medical device products across the UK and European market. This role monitors evolving UK and European regulatory requirements, leads product certifi...Read More>>.

Welcony, Carmarthen, Wales, United KingdomRegulatory Affairs Clinical SpecialistWelcony, Carmarthen, Wales, United Kingdom1 day ago Be among the first 25 applicantsGet AI-powered advice on this job and more exclusive...Read More>>.

Location: Hybrid (City of London office for a minimum of 3 days per week) Length of Contract: Permanent (subject to a 6-month probation period) Holidays: 25 days per year, plus a break between Christmas and Ne...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>>.

Galderma Limited (UK) is seeking a Regulatory Affairs Manager for the UK & Ireland, based in London. The role leads local regulatory activities for medicinal products, medical devices and cosmetics where applicable, ensuring compliance, registrati...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>>.

Leo Cancer Care in the United Kingdom is seeking a Site Planner to design, coordinate, and execute facility layouts for advanced radiotherapy system installations. You will work with architects, contractors, and internal Order Fulfillment teams to...Read More>>.

TÜV Rheinland UK is seeking a Field Sales Executive to drive new business in the Medical Devices sector across defined UK regions. The role focuses on generating order income and revenue from new large and medium customers through visits and even...Read More>>.

A growing speciality pharmaceutical business is expanding its European Regulatory Affairs team with the addition of a new Senior Regulatory Affairs Manager position.In this role, you will be responsible for portfolio of innovative produc...Read More>>.

Join UsAt Vodafone, we’re not just shaping the future of connectivity for our customers – we’re shaping the future for everyone who joins our team. When you work with us, you’re part of a global mission to connect people, solve...Read More>>.

Join UsAt Vodafone, we’re not just shaping the future of connectivity for our customers – we’re shaping the future for everyone who joins our team. When you work with us, you’re part of a global mission to connect people, solve...Read More>>.

I’m supporting a UK-based clinical-stage biotechnology company with the appointment of a Senior Manager, Regulatory Affairs. This is a senior, hands‑on regulatory role supporting a development programme as it progresses into late-pha...Read More>>.

Are you an experienced Regulatory Affairs Specialist with a passion for medical devices? Do you have experience EU MDR and US FDA QSMR? We are working with a well-established, global med-tech company, with offices in Crewe, who specialis...Read More>>.

Ready to lead global regulatory strategy and influence the development of innovative oncology therapies on a worldwide scale? Proclinical is seeking an Associate Director of Regulatory Affairs to join a dynamic team in the oncology and p...Read More>>.

HSBC in London is seeking an HCIB Regulatory Affairs Senior Manager to oversee regulatory engagements and developments within MSS. The role is hybrid, based in London, with a comprehensive pay and benefits package and a focus on regulatory change...Read More>>.

HCIB Regulatory Affairs Senior Manager (MSS) Location: London, GB, E14 5HQ Brand: HSBC Area of Interest: Risk and Compliance Role Workstyle: Hybrid Worker Date: 3 Oct 2026 If you’re looking for a caree...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>>.

Arxada is looking for a Regulatory Affairs Specialist based in Manchester, UK. This part-time position offers a hybrid working model and involves delivering regulatory aspects of critical projects, managing post-submission activities, and providin...Read More>>.

Whiteoak Associates is seeking a Senior Regulatory Affairs Manager to lead the UK-based European Regulatory Affairs function for a coatings portfolio. The role involves managing UK and EU regulatory registrations and notifications, and supporting...Read More>>.

Medical Devices Project Leader - Warwick We're looking for a driven and technically credible Project Leader to take a leading role in our Warwick based medical devices team. This is a chance to shape genuinely impactful technologies gu...Read More>>.

Vitalograph Limited is seeking an experienced Product Manager to own and evolve the comPAS PFT Solutions portfolio across software and hardware. You will translate clinical workflows and technical considerations into actionable roadmaps and requir...Read More>>.

Flexible Medical Packaging Limited (FMP) is a leading provider of sterile and non-sterile healthcare packaging. The Head of Quality will lead QA and Regulatory Affairs, maintaining compliance with ISO 13485, MDR, GMP and FDA requirements where app...Read More>>.

VERTECH GROUP (UK) LTD in London is seeking a Software Safety Engineer to join a fast-growing technology business operating in a highly regulated, safety-critical environment. The role focuses on assessing software development processes and techni...Read More>>.

Teva Pharmaceuticals in the United Kingdom seeks a Senior Quality Manager, Device R&D to ensure QMS compliance for combination products from concept through industrialization and life-cycle management.You will review and approve project doc...Read More>>.