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 design and develop electronics for cutting-edge medical devices, contributing to life-saving technologies. You will join a dedicated medical devices team on-site in Cambridgeshire, tackling complex design chal...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 ensure quality across medical device projects in a growing Cambridge-based team. You will focus on quality assurance under ISO 13485, with advantageous knowledge of EN 60601, and contribute to technical files and t...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 lead cutting-edge development projects within a multidisciplinary medical devices team in Cambridge, driving from concept to commercialization. You will oversee cross-functional groups, ensuring timelines and...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 contribute to the design and development of cutting-edge medical devices, working within a multidisciplinary design team to deliver safe, reliable products. You will join a growing part of the business with clear c...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 will collaborate with engineers and scientists in Cambridge to invent and advance new medical devices. You work across multiple projects, solving complex problems while keeping pace with evolving Technologies and...Read More>>.

Overview In this role you will lead the development and execution of global regulatory strategies for international markets, shaping regulatory input across multiple programs. You will collaborate with regional teams to align clinical and c...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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

Zenovo is seeking an Embedded Software Engineer in Cambridge to develop software for medical devices. You will work on real-time control, sensor data handling and hardware integration in a collaborative engineering environment.The role focu...Read More>>.

The Stryker Group in Belfast offers a placement within the Regulatory Affairs & Compliance Engineering team. You will gain hands-on experience supporting product registrations, change management, and Eudamed documentation, while collaborating with...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>>.

5S Recruitment Limited is seeking a Project Engineer to lead medical device tooling and injection moulding initiatives in a regulated environment. Based in Cheshire, you will guide projects from handover to production release, coordinating cross-f...Read More>>.

Stryker Foot & Ankle is seeking a high-performing sales professional to drive growth across Yorkshire. You will meet and exceed sales objectives, represent Stryker as a market leader, and build strong relationships with surgeons and HCPs.Th...Read More>>.

Dräger is seeking a Field Service Engineer to carry out scheduled maintenance, repairs, installation and commissioning of breathing apparatus and gas detection equipment across Crawley, Surrey/Sussex region. You will support service managers and...Read More>>.