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>>.

Division / Function Global Regulatory Affairs, Regulatory Operations Job Title Director, Regulatory Affairs, Labelling Summary & Purpose Of The Position Responsible for leading the development and...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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

The Senior Manager, Regulatory Affairs will work with EU regulatory lead(s) and/or directly with global regulatory lead(s) and within cross-functional teams to facilitate submission of applications to EU and International health agencies (HA) f...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>>.

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>>.

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>>.