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 act as Ofcom’s lead contact for Scotland across consumer, telecoms, spectrum and postal duties. You will build relationships with senior government, Parliament, and industry stakeholders, and coordinate cross-tea...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 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>>.

A leading pharmaceutical company in the United Kingdom is seeking a Mid-Senior level Regulatory Affairs Specialist to provide regulatory input and support for new Marketing Authorisation Applications. The ideal candidate will have a strong background...Read More>>.

Global Innovation and Technology Centre, Back Lane, Melbourn, Hertfordshire, SG8 6DP, United Kingdom, Melbourn SG8 6DP, GBPA works with many of the world’s most innovative pharmaceutical, medical device and life sciences companies. Bas...Read More>>.

Regulatory Affairs and Quality Assurance Assistant – Medical Devices - CambridgeDue to the growth of a medical devices company based in Cambridge, there is need for a new Regulatory Affairs and Quality Assurance Assistant to work with...Read More>>.

AbbVie is seeking an experienced professional to lead International Regulatory Advertising and Promotion within Allergan Aesthetics. The role requires oversight of global guidelines, collaboration with Commercial, Medical, Legal and Compliance tea...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>>.

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>>.

Praxis Group seeks an experienced regulatory professional to support the Director of Investment and Regulatory Affairs, ensuring Praxis Trust (BVI) Limited remains compliant with all regulatory obligations. You will lead the Regulatory team and co...Read More>>.

Praxis is an independent, leading provider of bespoke private wealth, corporate administration and yacht services to companies, individuals and families across the world. Our expertise and experience is driven by recruiting and retaining...Read More>>.

Rapidly growing, family-owned manufacturing organisation in East Yorkshire seeks a Technical and Regulatory Associate to manage chemical regulatory compliance across lab and commercial activities. You will collate regulatory information, ensure CE...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>>.

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>>.

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>>.

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>>.

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>>.

Ensera Design is seeking a Business Development Manager to drive growth in its Design & Product Development business within the medical device sector. You will lead consultative engagements, develop strategic relationships with senior stakeholders...Read More>>.

Elevaris Medical Devices in the UK is seeking a Quality Inspector to join the production quality team. You will operate equipment to manufacture precision components and ensure outputs meet stringent customer specifications, working under the Qual...Read More>>.

Rayner in Worthing, West Sussex, is seeking an analytical engineer or technical specialist to own Product Risk Management for medical devices, developing and maintaining risk documentation and leading cross-functional risk reviews. You will facili...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>>.

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>>.

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>>.

The Recruitment Group is seeking Production Operatives to join an established client in the Abingdon area. You will assemble medical devices to design specifications and work in a production line environment to meet tight deadlines.You will...Read More>>.

Crux Product Design is seeking motivated Intern Project Managers to join our Bristol team for a 12-month placement starting summer 2027, supporting the delivery of some of the world’s most exciting product development projects.You will wo...Read More>>.

TRS Consulting in the United Kingdom is seeking a Medical Devices Technician to set up and support surgical camera systems, inspect and troubleshoot medical devices, and provide on-site client support to ensure equipment functionality for patient...Read More>>.