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>>.

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>>.

Regulatory Affairs Specialist (Food Ingredients) Recruiter @ Seven Search and Selection Ltd | Specialising in Retail & FMCG Our client: A global leader in ingredient solutions, supporting innovation across fo...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>>.

The Association of Foreign Banks (AFB) is seeking a candidate for a hybrid role in London focused on regulatory monitoring and communication. Responsibilities include drafting materials for members, attending meetings, and conducting research on poli...Read More>>.

Apsida Life Science are currently partnering with a global biopharmaceutical company recognised for developing innovative medicines that address complex and serious diseases. The organisation combines strong scientific expertise with a patient-...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>>.

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>>.

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>>.

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>>.

Inspiration Healthcare seeks a Head of Quality Assurance and Regulatory Affairs in the UK to lead the Quality Assurance and Regulatory Affairs function, ensuring MDR compliance and regulatory registration across key markets. The role drives a cult...Read More>>.

Job Purpose (Role Definition)The Head of Quality Assurance and Regulatory Affairs:will manage the Quality Assurance and Regulatory Affairs function.is appointed as the person responsible for regulatory compliance,...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>>.

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>>.

Lead regulatory activities for drug-device combination products from clinical development through to NDA/MAA submissions.Manage the preparation and delivery of regulatory dossiers, ensuring critical timelines are met.Supp...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>>.

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>>.

Regulatory Affairs Senior Specialist - InternationalLocation: BedfordThe VacancySwiss Precision Diagnostics (SPD) is a world leader in the research, design and supply of advanced consumer diagnostic products. SPD is a joint...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>>.

ARCA Consulting Ltd seeks an experienced Mechanical Engineering Manager for Medical Devices to lead cross-disciplinary product development programs. You will own technical direction, delivery, budgets and schedules while guiding mechanical, electr...Read More>>.

IQVIA is seeking a MedTech Field Service Engineer Technician to install hardware for automated dispensing systems in healthcare facilities. The role combines hands-on electronics with customer-facing responsibilities and requires travel.You...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>>.

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>>.

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>>.

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>>.

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>>.