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 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 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 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 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 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>>.

Regulatory Affairs Manager page is loadedRegulatory Affairs ManagerApply locations UK - High Wycombe, Buckinghamshire time type Full time posted on Posted 30+ Days Ago job requisition id JR100567Reporting into the Head of Te...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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

Scarlet in London is seeking an Applied Machine Learning Engineer to join the team building production ML systems for medical device certification. You will own meaningful problems with clinicians and engineers, shaping success metrics and guiding...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>>.

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>>.

The Scarlet Company Group is seeking a Software Regulatory Specialist to join Scarlet’s Devices function. You will assess software lifecycle processes for cutting-edge medical devices and translate complex regulatory topics into clear content fo...Read More>>.

Medtech Search Associates Ltd provided pay rangeThis range is provided by Medtech Search Associates Ltd. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.Base pay range...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>>.

Cure Talent Ltd in London is partnering with a growing medical device certification organisation to provide expert contractor support across auditing, technical and clinical assessment.This role is for specialists with significant device ex...Read More>>.

Kroo Bank Ltd in London is seeking a Compliance Manager to lead regulatory adherence across the business, support policy development, and help shape a customer-centred compliance culture. You will partner with product, risk, and operations to embe...Read More>>.

Sizewell C Company is seeking a Head of Regulatory Affairs to lead regulatory, licensing and compliance across the organisation. The role reports to the Safety, Security & Assurance Director and oversees Regulatory Affairs, Licensing, Nuclear Comp...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>>.

BDO UK LLP is seeking a Legal Counsel to join the Office of the General Counsel (OGC) and help protect the firm's practice. You will work closely with Partners and senior members to advise on risk and regulatory matters, and support a range of civ...Read More>>.

About Us Access Partnership is the frontier consultancy getting innovation into market faster across technology, AI, Space and Health. With over 150 experts across six continents, we help clients in government, private sector and industry...Read More>>.

Merck & Co., Inc. is seeking a hands-on Associate Director, Regulatory Affairs – Power Platform Solutions Specialist. You will implement and maintain Power Apps UI changes, manage Dataverse security and data models, and automate workflows across...Read More>>.

Moody's in London seeks an AVP, EMEA Regulatory Affairs to support regulatory strategy across the EMEA region through stakeholder engagement, thought leadership, and cross‑functional collaboration.The role manages relationships with regul...Read More>>.

At Moody's, we unite the brightest minds to turn today’s risks into tomorrow’s opportunities. We do this by striving to create an inclusive environment where everyone feels welcome to be who they are—with the freedom to exchange ideas, think...Read More>>.

Corin Group is seeking a Senior Software Quality Engineer to oversee software and system development activities across its Global Technology Team. You will ensure compliance with FDA, ISO, and European Medical Device standards and drive quality im...Read More>>.