Test Technician - Medical & Drug Delivery Devices Permanent | On-site Location: Great Chesterford area, Cambridgeshire - up to £28,000Are you looking to start or build your career in medical device testing? We're hiring a...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>>.

Department: Vicon Quality & Regulatory Compliance Location: Yarnton, Oxfordshire Description Are you interested in working on products at the very cutting edge of technology? Want to join Vicon, an Academy Award®-winning...Read More>>.

Regulatory Affairs Director Our client is a young, exciting publicly listed clinical‑stage company dedicated to transforming the lives of patients in its therapy areas. With its novel and proprietary drug products and current clinica...Read More>>.

CY Partners are excited to be supporting a global organisation in recruiting an enthusiastic, scientifically minded scientist to join their experienced regulatory team. This is an excellent opportunity to work in chemical regulatory affairs, wo...Read More>>.

Contract: Full-time, Permanent Are you ready to make a difference in the beauty industry? Join us at Boots as a Regulatory Manager within the No7 Beauty Company’s Research & Development team in Nottingham! At Boots, we wo...Read More>>.

Export Control and regulatory Coordinator Location: Swinton, ManchesterDepartment: Quality & ComplianceSalary: £32,000 – £40,000 per annum About Luxfer Luxfer MEL Technologies is a lea...Read More>>.

Regulatory Affairs Specialist We’re looking for a Regulatory Affairs Specialist to join us, working across multidisciplinary teams to support and enable breakthrough innovation. Cambridge Consultants is a global technology and...Read More>>.

The Regulatory Affairs (RA) Officer is primarily responsible for ensuring the appropriate licensing, marketing and legal compliance of Sun Pharma’s pharmaceutical and medical products in order to control the safety and efficacy of these produ...Read More>>.

Flexi Start Happy Hour Drinks Fridge (Thursdays & Fridays) #TEAMBULK ARE HIRING A REGULATORY AFFAIRS ASSOCIATE Bulk™ is on an incredible journey, with a mission to move the business from a manufacturi...Read More>>.

AbbVie in Maidenhead seeks a senior Regulatory Affairs professional to lead UK regulatory efforts and serve as primary regulatory contact for designated therapeutic areas, guiding MHRA submissions and supporting launches. The role aligns with the...Read More>>.

Burtons Manufacturing Co Ltd is seeking a Senior Software Developer to join our engineering team in Staplehurst, Kent. You will develop Windows and Linux software primarily in C++, with additional C#, .NET, and web languages for UI and device cont...Read More>>.

United States Digital Space LLC is seeking a Software Safety Engineer to assess software lifecycle processes and regulatory documentation for medical device software. You’ll work with our product, engineering and applied machine learning teams t...Read More>>.

United States Digital Space LLC is seeking a Medical Device Auditor to audit manufacturers’ quality management systems against ISO 13485, EU MDR and UK MDR. You will learn our audit methods and deliver clear conclusions to support certification...Read More>>.

Company Description About AbbVie AbbVie'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 remarkabl...Read More>>.

If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global coll...Read More>>.

Director Quality Assurance and Regulatory Affairs This range is provided by Metric Bio. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range Direct message...Read More>>.

View Rubicon Technical - The Regulatory Compliance Experts Head of Regulatory Affairs (Food Supplement) Company Overview: Rubicon Bridge is a fast-growing SaaS provider to the consumer healthcare and wellness industry. We are...Read More>>.

Rubicon Bridge Ltd. is seeking a Head of Regulatory Affairs (Food Supplement) to lead global regulatory strategy for supplements. You will steer regulatory decisions, liaise with product and tech teams to embed compliance, and interact with major...Read More>>.

Who we are At Twilio, we’re shaping the future of communications, all from the comfort of our homes. We deliver innovative solutions to hundreds of thousands of businesses and empower millions of developers worldwide to craft persona...Read More>>.

Crux Product Design Ltd. in Bristol is seeking a talented Project Manager to oversee the development of medical and consumer goods devices from concept through production.You will coordinate design and engineering teams, manage timelines, b...Read More>>.

AND Digital Limited is seeking four Embedded C++ Developers to join an in-house backend team on a highly regulated medical technology product in London. You will own a self-contained area of the application from design through tested, documented c...Read More>>.

Newton Colmore Consulting in Cambridge is seeking an embedded software engineer to work on diagnostics technologies for the Medical Devices and Life Sciences sectors. The role is permanent and full-time, with an excellent starting salary and compr...Read More>>.

ECM Selection (Holdings) Limited seeks an experienced embedded C/C++ developer to join a multidisciplinary engineering team. You will work on medical technology projects, from on-board device software to driven hardware interfaces, with direct cli...Read More>>.

Product Security Specialist for Medical Devices (Cyber Security) We believe in the power of ingenuity to build a positive human future. As strategies, technologies, and innovation collide, we create opportunity from complexity....Read More>>.

AND Digital is seeking four Embedded C++ Developers for an in-house backend engineering team working on a highly regulated medical technology product in London. You will own a self-contained area of the application and drive design through to test...Read More>>.

eg technology is seeking a capable project leader to drive complex product development projects from concept through manufacture. You will coordinate software, electronics, mechanical engineering, industrial design and human factors teams, ensurin...Read More>>.

OrganOx Limited is seeking a Senior IP Specialist to define and execute the company’s global IP strategy. The role acts as the internal authority on IP matters and collaborates with R&D, regulatory, and business teams to protect and exploit the...Read More>>.

Maclivaro Limited is seeking an experienced Operations Manager to lead manufacturing, warehousing, supply chain and QA at our Houghton Regis site. You will drive performance, optimise processes and contribute to the longer-term strategic plan....Read More>>.

Gold Group is seeking an Electrical Engineer for medical devices in Cornwall. You will design electrical systems, develop schematics and PCBs, verify and validate devices, and ensure EMC/safety compliance while collaborating with global R&D teams....Read More>>.

Bluetree Recruits is seeking a Senior Regulatory Affairs & Quality Manager in Cambridge to shape regulatory strategy for the US first and expand globally. You will own FDA, CE and UKCA submissions and lead a robust QMS, partnering with leadership...Read More>>.

McAllister Recruitment are recruiting on behalf of our client a leading company in the Wound Care and Medical Device space. This is an opportunity to represent an innovative healthcare solutions company whose product portfolio is well represented...Read More>>.

University Intern - Regulatory Affairs - UK, Ireland and MaltaNumber of opportunities: 1Salary: £26,000 (Not flexible)Closing date: 26/10/2026This is a 12-month paid internship starting September...Read More>>.

Sanofi offers an industrial placement in Regulatory Affairs at our Reading Head Office. You will gain hands-on experience supporting regulatory submissions for medicines and vaccines in the UK and Ireland, under mentors and cross-functional teams....Read More>>.

Neucin Design Ltd is a growing engineering consultancy specializing in medical devices. We seek an Engineering Technician to provide hands-on testing, prototyping, instrument care and documentation to support engineers in design and development....Read More>>.

Sanofi offers an industrial placement in Regulatory Affairs at Reading (Head Office). You will gain hands-on experience across UK/Ireland regulatory activities, under mentorship, while contributing to lifecycle management of medicines and vaccines...Read More>>.

Role Overview MedScope, a leader in the healthcare industry since 1999, supports tens of thousands of Personal Emergency Response System (PERS) users nationwide. Our work helps individuals—many of whom are Medicaid members—remain safe...Read More>>.

Job DescriptionWe are looking for an experienced Senior to support the UK Medical Devices Team to coordinate & support the process for Technical Documentation Reviews & monitor KPI reports and coordinate resultant actions as needed....Read More>>.

SGS is looking for an experienced Senior to support the UK Medical Devices Team with Technical Documentation Reviews and KPI monitoring. You will coordinate TD reviews, assist with complaints, and support key client calls and meetings, ensuring ac...Read More>>.

Johnson & Johnson is recruiting an Import/Export Operations Specialist based in Leeds, United Kingdom. You will manage day-to-day import and export operations to ensure on-time delivery and regulatory compliance within a fast-paced medical device...Read More>>.

Olympus Corporation is seeking a Territory Manager to promote the gastroenterology product range across Liverpool, North Wales, Lancashire, Cumbria and Shrewsbury and Telford. The role focuses on driving sales, building relationships with hospital...Read More>>.

The Medical Equipment Library Assistant ensures vital medical devices are available, clean, safe, and ready for patient use. They coordinate the management of high-demand equipment, log and process faulty devices, and work alongside the Clinical E...Read More>>.

TÜV Rheinland Europe is seeking a Medical Device Assessor/Auditor with a background in medical device design, manufacturing, or quality control. The role involves planning and conducting audits at client sites, reviewing documentation, and ensuri...Read More>>.

The Walton Centre NHS Foundation Trust is seeking a Medical Devices Safety Officer (MDSO) to provide Trust-wide leadership and assurance for medical device safety, governance and regulatory compliance. The postholder will lead safety alerts manage...Read More>>.

Entrust Resource Solutions in Livingston is seeking a Production Operator to join an established medical device manufacturer. The role focuses on packing products in a quality-focused environment, adhering to procedures and maintaining cleanliness...Read More>>.

Johnson & Johnson invites applications for a 12-month internship in Leeds, within the Quality/Sterility Assurance team of DePuy Synthes. You will gain hands-on experience across the full product lifecycle—from design through terminal sterilizati...Read More>>.

Kinetica in South Wales is seeking a Junior/Quality Engineer to join our medical device quality team. You will support QA activities, investigate quality issues, and assist with CAPA initiatives to ensure regulatory compliance.The role offe...Read More>>.