United States Digital Space LLC is seeking a talented Software Engineer Embedded Firmware to join their Crawley office. This role involves designing, implementing, testing, and maintaining firmware for innovative radiation therapy medical devices....Read More>>.

Regulatory Affairs Advisor – Hybrid To c£45,000 + package Worcester, Redditch, Evesham, Warwick, Cheltenham, Tewkesbury, Droitwich Spa, region around WR11.This business is an international leader in manufacturing and raw material...Read More>>.

Company DescriptionAbbVie'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...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>>.

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>>.

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>>.

1 week ago Be among the first 25 applicantsDirect message the job poster from Hartmann YoungHeadhunter | Specialising in Diagnostics & Genomics | Connecting Top Talent across the Industry Associate Director – Regu...Read More>>.

Regulatory Affairs Specialist (Manchester, UK – hybrid, part‑time) As a Regulatory Affairs Specialist you will play a vital role in enabling Arxada’s continued growth and market access across the EMEA region. Working within the M...Read More>>.

Revolut is seeking an experienced Regulatory Affairs Manager to lead interactions with external regulators and ensure ongoing compliance as the company expands its regulated fintech operations. You will translate complex regulatory proposals into...Read More>>.

Pfizer Inc. is seeking a Senior Regulatory Manager to drive regulatory strategy for assigned products and markets. You will partner with cross-functional teams to obtain and maintain marketing authorizations and support clinical trial applications...Read More>>.

Skills Alliance seeks an SVP Regulatory Affairs / Chief Regulatory Affairs Officer for a leading biotech with a pivotal Phase 3 programme. Lead global regulatory strategy, oversee NDA/MAA submissions and engage with FDA/EMA to drive speed to appro...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>>.

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>>.

Enterprise Recruitment Ltd is seeking an experienced systems engineer to work on a cutting-edge medical devices project within a world-leading system rollout. Based in a state-of-the-art Surrey facility, you will collaborate with electronics, soft...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>>.

Electrical Engineer - Medical Devices (BBBH73810) Falmouth, England Electrical / Electronics Engineer – Medical Devices Cornwall, UK (On-site) Global Healthcare Organisation | Women's Health & Medical Technology An excit...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>>.

Smith Nephew in the UK is seeking a Quality Engineer to own the quality performance across a Manufacturing Value Stream. You will apply SPC, Six Sigma, and data-driven metrics to drive process stability, proactive risk identification and continuou...Read More>>.

CV TECHNICAL LTD is seeking a Senior Automation Engineer in Dorset to lead automated assembly projects from concept through commissioning, validation and full production implementation. You will collaborate with Operations, Quality, R&D, Validatio...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>>.

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>>.

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 bring...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>>.

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>>.

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>>.

MSD in the UK invites applications for a 24-month Regulatory Affairs Graduate Programme with rotations across International Regulatory Affairs CMC and UK Regulatory Affairs. You will gain exposure to regulatory strategy, submissions, and health au...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>>.

Baxter Healthcare is seeking a Field Engineer to deliver service activities on Baxter/Hillrom products across defined UK regions in compliance with company procedures and safety standards.Key duties include installation, service, repair, ca...Read More>>.

Office Angels is seeking a Senior Sales Account Manager for Scotland to grow existing accounts and win new business within the National Health Service. This role requires strong medical devices sales and account management skills, plus an understa...Read More>>.

Stryker Corporation in the United Kingdom is seeking an Associate Sales Representative to start a career in medical devices. You will work with an experienced team to grow Neuro and Spine business, develop relationships with surgeons and hospital...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>>.

Johnson & Johnson–DePuy Synthes in Leeds offers a 12-month non-LDP Intern/Co-Op in the Quality/Sterility Assurance area. You’ll work with scientists, engineers and production teams, gaining hands-on experience across the full product lifecycle...Read More>>.