Overview You lead a global Medicines Lifecycle Management team to deliver post-approval regulatory strategy and ensure compliant, timely submissions across a diverse portfolio. You translate regulatory needs into practical plans, partnering...Read More>>.

Overview As Director of Structured Content Authoring, you will lead the move from document-centric regulatory operations to a data-driven, component-based model. You’ll set vision, governance and a roadmap that links regulatory content, m...Read More>>.

Overview In this role you lead Perrigo's global Regulatory Affairs Lifecycle Management for Medicines, shaping strategies across the full product lifecycle. You will drive end-to-end dossier development, submissions, and maintenance to meet...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 role, you will assess and improve quality management systems for software-based medical devices, ensuring regulatory compliance and robust processes. You’ll work within a cross-functional context to strengthen QMS and sup...Read More>>.

Overview In this role you lead drug delivery and combination product programmes from concept to industrialisation within PA’s life sciences practice. You provide senior technical leadership across engineering, usability, risk and manufact...Read More>>.

Overview In this role you will help invent and improve Medical Devices within a collaborative, multi-disciplinary environment in Cambridge. You’ll translate inventive ideas into practical devices across drug delivery, diagnostics, wearabl...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 In this role you will drive the design and development of innovative medical devices within a multidisciplinary team. You will turn concept ideas into robust, manufacturable hardware through hands-on mechatronics work. You’ll col...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>>.

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>>.

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>>.

Are you immediately available and looking for a new opportunity with a global food manufacturer? Do you have prior compliance or specifications technologist experience?Due to an increase in workload, a successful, globally recogni...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>>.

Sizewell C is recruiting a Head of Regulatory Affairs to lead regulatory, licensing, compliance and integrated management systems across a major UK energy project. This senior role reports to the Safety, Security & Assurance Director and shapes re...Read More>>.

Cure Talent are delighted to be partnered with a growing medical device certification organisation that is expanding its technical and clinical assessment capability across a number of new medical device categories. We are looking to spe...Read More>>.

We pull medical technology from the future to solve human health. Scarlet is authorised to assess and certify medical devices. We combine clinical, technical and regulatory expertise with AI agents and software so rigorous certificatio...Read More>>.

SPD Swiss Precision Diagnostics GmbH in Bedford, UK, is seeking a Senior Regulatory Affairs Specialist - International to lead regulatory strategies for global markets. The role offers hybrid working and a permanent contract, with responsibilities...Read More>>.

Neko is redefining what prevention means, from treating illness when it arrives, to sustaining health before it's ever at risk. Our mission: make data-driven, preventative care accessible to more people, before symptoms appear. In a single,...Read More>>.

Neko Health AB seeks a regulatory affairs engineer to own the clinical regulatory work for our devices, drafting clinical evaluation plans and reports and supporting submissions to the FDA, EU and UK.The role spans hardware and software, co...Read More>>.

Leo Cancer Care is seeking a Mechanical Engineering Lead to drive robust, safe, and manufacturable designs for cancer treatment equipment. You will lead a small team within a regulated environment, coordinating with electronics, systems, software,...Read More>>.

JOB DESCRIPTION: About the Role We are seeking an experienced and results-driven Manager, Medical Devices Service Centre to lead a critical service operation supporting our medical device portfolio. This role is responsible for delivering exceptio...Read More>>.

Flusso Ltd. seeks a Senior Firmware Engineer to develop real-time firmware for ARM-based microcontrollers and ASIC cores, and to port firmware to new processors. The role supports sensor products, evaluation kits, and PC interfaces, with a strong...Read More>>.

Newton Colmore Consulting is working with a medical devices company based in Cambridgeshire to recruit a Mechatronics Design Expert to lead the design of next-generation machines. This role offers the chance to work on cutting-edge medical technol...Read More>>.

Haleon plc seeks an experienced Regulatory Affairs Manager to manage a defined GB&I product portfolio, ensuring proactive compliance with UK, Irish and European laws. You will oversee submissions, claims advice, and labeling while coordinating wit...Read More>>.

Corin is seeking a motivated individual to join our Quality Control team as a Quality Inspector Assistant in Cirencester. This entry-level role offers comprehensive training to develop into a full Quality Inspector, with exposure to product inspec...Read More>>.