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 lead regulatory activities for Galderma’s medicinal products across the UK and Ireland, ensuring regulatory compliance and lifecycle management. You will shape local regulatory strategy in partnership with...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 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 integrate regulatory thinking with engineering to support a diverse portfolio of complex projects in Cambridge. You’ll work closely with design engineers, scientists and project teams to ensure development pathwa...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 support regulatory activities across the business, collaborating with engineers and scientists to align development with global requirements. You will help operate the quality management system and guide teams thr...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>>.

Office of Regulatory Relations, Regional Country Compliance, Vice President, London location_on London, Greater London, England, United Kingdom OUR IMPACT The Office of Regulatory Relations (ORR) protects the firm’s regulatory...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>>.

Contract: Full-time, Permanent Are you ready to make a difference in the beauty industry? Join us at Boots as a Regulatory Manager within the No7 Beauty Company’s Research & Development team in Nottingham! At Boots, we wo...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>>.

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>>.

Regulatory Affairs Director Our client is a young, exciting publicly listed clinical‑stage company dedicated to transforming the lives of patients in its therapy areas. With its novel and proprietary drug products and current clinica...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>>.

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>>.

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>>.

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>>.

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>>.

Job Description 12-Month Regulatory Affairs CMC Student Placement offering exposure to regulatory strategy, submissions management, health authority engagement, and operational excellence projects. Our Regulatory Affairs team...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>>.

University Intern - Regulatory Affairs - UK, Ireland and MaltaNumber of opportunities: 1Salary: £26,000 (Not flexible)Closing date: 26/10/2026This is a 12-month paid internship starting September...Read More>>.

Sanofi offers an industrial placement in Regulatory Affairs at our Reading Head Office. You will gain hands-on experience supporting regulatory submissions for medicines and vaccines in the UK and Ireland, under mentors and cross-functional teams....Read More>>.

Sanofi offers an industrial placement in Regulatory Affairs at Reading (Head Office). You will gain hands-on experience across UK/Ireland regulatory activities, under mentorship, while contributing to lifecycle management of medicines and vaccines...Read More>>.

Register Your Interest - Government & Regulatory Affairs Placement 2027To join one of our 12-month Internships you will be:Currently be an undergraduate studying at University and applying for a Placement year in your 2nd or f...Read More>>.

Environmental Health Officer (EHO) / Senior EHO / EH Regulatory Officer / Senior EHRO Salary £36,555 - £54,804 p.a. (dependent on experience) plus essential user car allowance plus a Recruitment Allowance of £5,480 Full-time (36...Read More>>.

CPL Aromas is seeking a Regulatory Support Specialist for a 12-month fixed-term contract. You will provide guidance on regulatory requirements for fragrances, share knowledge with global teams, and ensure formulations comply with current legislati...Read More>>.