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>>.

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>>.

Network Scientific Recruitment partners with a global med-tech company with Crewe offices to recruit a Senior Regulatory Affairs Specialist. The role defines and leads regulatory strategies for assigned portfolios, guiding EU MDR and US FDA submis...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>>.

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>>.

OverviewAt BioTalent, we are working with a client exclusively to fill their RA Specialist position. They are a fast growing CGT company focused on developing products in the immuno-oncology. This role will focus on supporting their exist...Read More>>.

Job DescriptionRegulatory Affairs SpecialistLocation: Hybrid – Kent/LondonJob Type: Full-time, PermanentAbout the RoleAn exciting opportunity has arisen for a Regulatory Affairs...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>>.

Senior Regulatory Affairs Manager - Chemicals / Paints / Coatings / ResinsNorthumberland - near Newcastle Upon Tyne | 4 days on siteA rare opportunity has arisen for an experienced Senior Regulatory Affairs Manager to join an inter...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>>.

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>>.

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>>.

Teva Pharmaceuticals in the United Kingdom seeks a Senior Quality Manager, Device R&D to ensure QMS compliance for combination products from concept through industrialization and life-cycle management.You will review and approve project doc...Read More>>.

Medtronic Digital Technologies is seeking a Senior Software Engineer to advance intra-operating device software using modern C++ (C++17+), across embedded, application, and cloud teams. You will own maintainability and help build the software stac...Read More>>.

Medtronic is seeking a Software Development Engineer in Test to design and build automated test solutions for device software, firmware, and hardware-software interfaces. You will work with embedded and edge technologies, including Android/Linux,...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>>.

OrganOx Limited is seeking a Windows Software Manager to lead the design and development of software for organ-perfusion devices used in regulated medical environments. The role focuses on GUI, connectivity, cybersecurity, and end-to-end ownership...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>>.

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>>.

Job Description 12-Month Regulatory Affairs CMC Student Placement offering exposure to regulatory strategy, submissions management, health authority engagement, and operational excellence projects. Our Regulatory Affairs team...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>>.

Boehringer Ingelheim in Winnersh, UK, is offering a 12-month paid internship in Regulatory Affairs for the UK, Ireland and Malta, starting September 2027. The role requires a minimum of two days per week at the head office and provides exposure to...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>>.

Register Your Interest - Government & Regulatory Affairs Placement 2027To join one of our 12-month Internships you will be:Currently be an undergraduate studying at University and applying for a Placement year in your 2nd or f...Read More>>.

MSD in the UK offers a 12-month Regulatory Affairs CMC student placement in Moorgate, London, exposing you to regulatory strategy, submissions management, health authority engagement, and operational excellence projects.We are a global biop...Read More>>.

Entrust Resource Solutions is recruiting a Production Operator to join an established medical device manufacturer in Livingston. This hands-on role involves packing products in a quality-focused manufacturing environment, where accuracy, cleanline...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>>.

MedScope Installation is seeking self-motivated field technicians to join a 1099 independent contractor program. You will coordinate installations, perform delivery, setup and testing of PERS devices in clients' homes, and educate users on device...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>>.

Rayner is seeking a seasoned Project Manager to lead innovative new product development and process improvements from concept to launch at our Worthing HQ. You will drive cross-functional projects and build strong relationships with Regulatory, Qu...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>>.

SRG is recruiting for a Cambridge-based internship within the Device Engineering team. The role involves CAD design, technical analysis, prototyping, lab testing and reporting as part of a year-long development journey with mentorship.Ideal...Read More>>.

SGS is seeking an organised professional to support the UK Medical Devices Team in delivering activities to the required standards and timescales. You will handle contract reviews, change notifications and proposals while ensuring accurate invoici...Read More>>.

Invibio, part of the Victrex plc group, seeks a Quality Engineer to embed quality in design and development of medical technologies. You will apply QMS and design controls across projects, collaborating with internal teams and external suppliers t...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>>.

Johnson & Johnson is recruiting an Import/Export Operations Specialist for Leeds, UK. The role focuses on compliant, timely movement of DePuy Synthes products across borders, managing customs processes, trade docs, and regulatory needs in a highly...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>>.