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>>.

Export Control and regulatory Coordinator Location: Swinton, ManchesterDepartment: Quality & ComplianceSalary: £32,000 – £40,000 per annum About Luxfer Luxfer MEL Technologies is a lea...Read More>>.

Regulatory Affairs Specialist We’re looking for a Regulatory Affairs Specialist to join us, working across multidisciplinary teams to support and enable breakthrough innovation. Cambridge Consultants is a global technology and...Read More>>.

The Regulatory Affairs (RA) Officer is primarily responsible for ensuring the appropriate licensing, marketing and legal compliance of Sun Pharma’s pharmaceutical and medical products in order to control the safety and efficacy of these produ...Read More>>.

Flexi Start Happy Hour Drinks Fridge (Thursdays & Fridays) #TEAMBULK ARE HIRING A REGULATORY AFFAIRS ASSOCIATE Bulk™ is on an incredible journey, with a mission to move the business from a manufacturi...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>>.

Advanced Medical Solutions is seeking a UK-based international medical sales professional to grow the wound care portfolio. You will hunt new business, expand product offerings, and drive revenue across defined territories, including contract manu...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>>.

Energy Jobline ZR is seeking a Senior Embedded Software Engineer in Runcorn with a flexible hybrid work arrangement. You will own embedded software across a medical device portfolio, defining architecture and standards while ensuring quality, docu...Read More>>.

TRS Consulting is seeking a Field Service Engineer to service and repair our range of advanced medical systems and healthcare equipment across client sites in the UK. You will diagnose faults, perform routine and corrective maintenance, install up...Read More>>.

TRS Consulting in Witney is seeking a Field Service Engineer for Medical Devices to service and repair a range of advanced medical systems and healthcare equipment onsite.The role requires hands-on experience with electronic, electrical and...Read More>>.

TRS Consulting is seeking a Field Service Engineer to service and repair a range of advanced medical systems and healthcare equipment. You will apply your electronics, electrical and mechanical expertise on-site with our clients across the region....Read More>>.

Network Scientific Recruitment partners with a global med-tech company with Crewe offices to recruit a Senior Regulatory Affairs Specialist. The role defines and leads regulatory strategies for assigned portfolios, guiding EU MDR and US FDA submis...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>>.

Company Description About AbbVie AbbVie'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 remarkabl...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>>.

Job Description The Director, Structured Content Authoring is a transformational leadership role responsible for accelerating the organisation's evolution from document-centric regulatory operations to a modern, data-driven and compon...Read More>>.

W Talent are delighted to be partnering with an established manufacturing business to recruit a Regulatory Affairs Specialist. This is an opportunity to join a growing Technical function, supporting regulatory compliance and ensuring products m...Read More>>.

Clearline Recruitment Ltd in Motherwell, Scotland, onsite, is seeking a Product Definition Lead for a 12-month contract. You will lead the product definition of technically complex point-of-care systems across instrument, assay and disposable deve...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>>.

Gold Group Limited in London (West W6) is seeking a Human Factors Consultant to join our team, helping design medical device products, services, and experiences that are safe and intuitive within the healthcare sector.You will work with res...Read More>>.

Afferent Medical Solutions Ltd. in Cardiff seeks a skilled Software Architect to design a new software system for a ground-breaking medical treatment. You will work within a small team across research, design, implementation, release and post-rele...Read More>>.

Elevaris Medical Devices is seeking a Quality Inspector to join the Legal, Quality & Regulatory Affairs team in Thornaby, Stockton-on-Tees, United Kingdom. The role reports to the Quality Manager and is offered on a permanent contract.You w...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>>.

Newton Colmore in Warwick is seeking a Medical Devices Project Leader to drive product development from concept through to commercial launch in a fast-moving, multidisciplinary team.You will lead complex engineering challenges for high-volu...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>>.

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>>.

Are you an experienced sales professional looking to take the next step in your career? This is a fantastic opportunity to join a fast-paced, forward-thinking organisation that delivers innovative medical products and services to hospi...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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

Albus Health in Oxford is seeking a senior medical-device verification engineer for an initial three-month contract with potential extension. You will strengthen verification evidence and regulatory documentation for FDA submissions.You wil...Read More>>.