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 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 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>>.

Regulatory Affairs Manager page is loadedRegulatory Affairs ManagerApply locations UK - High Wycombe, Buckinghamshire time type Full time posted on Posted 30+ Days Ago job requisition id JR100567Reporting into the Head of Te...Read More>>.

Head of Regulatory Affairs – UK & Ireland An outstanding opportunity has arisen within a leading, innovation-driven pharmaceutical company dedicated to delivering value-based, patient-centric healthcare solutions. As Head of Regulato...Read More>>.

Department: Vicon Quality & Regulatory Compliance Location: Yarnton, Oxfordshire Description Are you interested in working on products at the very cutting edge of technology? Want to join Vicon, an Academy Award®-winning...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>>.

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>>.

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

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing der...Read More>>.

Corza Medical is seeking a Graduate Manufacturing Engineer to join our manufacturing team in Taunton. You will support validation, optimization, and continuous improvement of processes in a regulated medical device environment (ISO 13485 and FDA),...Read More>>.

Synergy Spine Solutions is seeking a Director of Sales (International) to own and grow the business outside the United States. You will lead and scale distributor networks across EMEA, APAC, and Canada, while shaping market access, training, and r...Read More>>.

Can you turn regulatory complexity into commercial success while guiding the launch of tomorrow's market-leading products? R&D Partners is seeking a Regulatory Affairs Manager to join a leading pharmaceutical company. This role offers an...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>>.

About ECI ECI’s mission is to be the global leader of professional consulting services for the life sciences industry. Our clients lean on our diverse perspectives and decades of expertise to tackle their toughest challenges, and we tak...Read More>>.

About ECI ECI’s mission is to be the global leader of professional consulting services for the life sciences industry. Our clients lean on our diverse perspectives and decades of expertise to tackle their toughest challenges and we take...Read More>>.

Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled wi...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>>.

Cure Talent Limited is partnering with a growing healthcare technology company to recruit a QA Specialist for a six‑month fixed‑term contract based in London with hybrid on-site one day per week. The role focuses on strengthening the quality m...Read More>>.

Godwin Recruitment in Birmingham seeks a Material Specialist to strengthen raw material security by locating, ordering and testing alternative materials within the Scientific Research Department. The role involves material evaluation, supplier eng...Read More>>.

Overview You’ve learned a lot as a student already. Want to put it into practice at PepsiCo? Our placement programmes are structured to give you the chance to make an impact on some of the world’s biggest brands. From day on...Read More>>.

Progress Sales Recruitment is seeking a Business Development Manager for theatre products and surgical instruments. The role is home based across the North East England and Scotland, covering cities such as Newcastle, Leeds, Sunderland and beyond,...Read More>>.

Scarlet is seeking an Applied Machine Learning engineer to own meaningful problems in how we assess medical devices: define success with domain experts, decide what to build and test, and take ML systems through deployment and measurable improveme...Read More>>.

Vertech Group (UK) Ltd in London is seeking a Safety Software Engineer to join a team evaluating software development processes and technical evidence underpinning AI-enabled medical devices. You will review software lifecycle, V&V, configuration...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>>.

Welcome to the era of Velsera! Seven Bridges, Pierian & UgenTec have combined to become Velsera.Velsera is the precision engine company. We empower researchers, scientists, and clinicians to drive precision R&D, expand access to, and m...Read More>>.

Can you turn regulatory complexity into commercial success while guiding the launch of tomorrow’s market-leading products?R&D Partners is seeking a Regulatory Affairs Manager to join a leading pharmaceutical company. This role offers a...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>>.

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>>.

MSD invites applications for a 12-month Regulatory Affairs CMC student placement in London. You will gain exposure to regulatory strategy, submissions management, health authority engagement, and operational excellence projects.The role is...Read More>>.

Haemonetics Interventional Technologies is seeking a Field Service Engineer to install, service, repair and maintain a portfolio of devices across South East England and Midlands. You will travel within your region and the UK, providing applicatio...Read More>>.