Cure Talent are delighted to be partnered with a growing diagnostics company based near Cambridge. As they continue to progress their existing medical devices and move towards the next stage of their IVD development programme, we have an exciting...Read More>>.

Quality Engineer (Medical Devices) £40,000 - £43,000 + Bonus + Sick Pay + Life Assurance + 33 Days Holiday Andover, HampshireAre you a Quality Engineer from a medical devices background, looking to utilise your kn...Read More>>.

Overview In this role you integrate regulatory thinking with engineering to support a diverse portfolio of complex projects in Cambridge. You’ll work closely with design engineers, scientists and project teams to ensure development pathwa...Read More>>.

Overview In this role, you support regulatory activities across the business, collaborating with engineers and scientists to align development with global requirements. You will help operate the quality management system and guide teams thr...Read More>>.

Overview In this role you will lead European regulatory strategy for oncology products, accelerating approvals and securing strong labels. You will represent AstraZeneca with European regulators, steering high-stakes meetings and shaping gl...Read More>>.

Overview In this role you will drive regulatory strategies and submissions for cutting-edge medical devices and IVDs in the EMEAP region. You will collaborate within a global team to accelerate market access and meet regulatory requirements...Read More>>.

Cambridge, Cambridgeshire, United KingdomSenior Regulatory Affairs Specialist - CambridgeAt Hologic, we are committed to enabling healthier lives everywhere, every day. To deliver on that purpose, we need strong regulatory...Read More>>.

Crux Product Design in Bristol, UK is seeking an Advanced Human Factors Engineer to lead usability work across medical device programs. You will plan, run and report on studies, ensuring user needs are integrated early and throughout development t...Read More>>.

Adepto Technical Recruitment Ltd is assisting a large CDMO in Hampshire, UK, to recruit a Quality Assurance Specialist for pharmaceutical and Medical Device products. The role focuses on investigating customer quality issues, non-conformities, and...Read More>>.

ECI, based in the United Kingdom, seeks a Project Manager to lead cross-functional teams and drive complex medical device projects from planning through execution. You will manage scope, schedule, and budget while coordinating with customers and i...Read More>>.

ECI is seeking a seasoned Project Manager to lead the design and development of complex mechanical medical devices. You will ensure alignment across disciplines, manage scope, schedule, and risk, and coordinate with sponsors and vendors to deliver...Read More>>.

This is a Part-time position, between 16-20 hours a week.You’re comfortable working where detail matters. Managing documentation, supporting compliance processes, and keeping quality systems running smoothly behind the scenes. Y...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>>.

Hollybank Trustees Ltd seeks a Head of Quality Assurance and Regulatory Affairs to lead the QA and regulatory function in a hybrid role with Croydon, UK. You will shape the QA strategy, oversee compliance with MDR, ISO 13485 and MDSAP, and manage...Read More>>.

Head of Quality Assurance and Regulatory Affairs Location: Hybrid / Croydon, UKjob type: Permanent / Full-timeSector and subsector: Medical & Healthcare | OtherSalary: Competitive salary...Read More>>.

SVP Regulatory Affairs / Chief Regulatory Affairs OfficerLocation: UK, Germany or United StatesConfidential search | Late-stage biotechnologyThe opportunityA late-stage biotechnology company developing nov...Read More>>.

Select Pharma Recruitment is seeking an experienced Regulatory Affairs Manager for a growing generic pharmaceutical company in the UK. The role is onsite five days per week, focusing on post-approval compliance, variations, license transfers and M...Read More>>.

Develop embedded C and C++ software to bring new medical technology to life Looking for an embedded development role with variety, client-contact, and a positive real-world impact? This role may be just the ticket: a well-established medi...Read More>>.

OrganOx seeks a Senior IP Specialist to define and execute its global IP strategy, aligning with R&D and business objectives. This role holds autonomy as the primary internal authority on IP matters and guides decisions across product development...Read More>>.

Siemens Healthineers UK is seeking an experienced Quality Engineering leader to oversee a team of Quality Engineers and Technicians. You will drive performance, develop staff, and ensure alignment with site objectives and regulatory requirements....Read More>>.

Siemens Healthineers in Sudbury, UK, is seeking an Automation Engineer to join the Point of Care Diagnostics team. You will maintain and develop the site's automation, controls and OT capabilities, providing onsite technical ownership for PLC, SCA...Read More>>.

Salary: £45,000 - 85,000 per year Requirements: We require experience as an Embedded Software Engineer, with a strong track record of problem solving using C and other software languages. We prefer experience...Read More>>.

Embla Medical in Livingston is seeking a Senior Mobile Apps Developer to strengthen the Össur R&D team. You will design, develop and test mobile apps and cloud services that connect patients and clinicians with our devices.You will work ac...Read More>>.

AND Digital is seeking four Embedded C++ Developers to join an in-house backend team in London. You will own modules from design through to tested and documented code on a Linux-based, safety-critical medical tech product.Work spans alarms,...Read More>>.

Olympus is seeking a commercially driven Senior Territory Manager to grow our surgical devices and endoscopy business across Yorkshire, Lancashire, and Sheffield. You will build trusted relationships with healthcare professionals and hospital team...Read More>>.

Star People client in North West England is seeking a Territory Manager to maximise sales of medical and surgical devices through face-to-face engagement with clinicians and staff. You will promote product solutions, deliver training, and provide...Read More>>.

About the Role 24-Month Regulatory Affairs Graduate Programme featuring rotations in International Regulatory Affairs CMC and UK Regulatory Affairs, with exposure to regulatory strategy, submissions, compliance, and health authority en...Read More>>.

Peopleforce Recruitment Ltd is recruiting a Regulatory Affairs Specialist for Dundee, office-based, to reinforce the Compliance Team. The role focuses on ensuring that products, processes and quality systems meet UK, EU, Swiss and international re...Read More>>.

Guided Solutions is supporting an established medical device business expanding its UK commercial team. The NHS Territory Manager role offers a commercially minded sales professional the chance to own a territory and progress within healthcare sal...Read More>>.

Caraway Therapeutics, Inc. in London offers a 24-month Regulatory Affairs Graduate Programme with rotations in International Regulatory Affairs CMC and UK Regulatory Affairs. The role provides exposure to regulatory strategy, submissions, complian...Read More>>.

Alliance Pharma PLC in Chippenham, Wiltshire, offers a hybrid Regulatory Affairs Associate role (VMS/Food Supplements) for a 9-month maternity cover starting November 26. The post supports maintenance and development of an EMEA portfolio across VM...Read More>>.

This is a 12-month paid internship starting September 2027. The role is head office based requiring a minimum of 2 days a week to be worked from our office in Winnersh. INTRODUCING THE OPPORTUNITY Joining Boehringer Ingelheim in September 2027, yo...Read More>>.

STADA UK Thornton & Ross in Huddersfield invites applications for a 12-month Regulatory Affairs placement student commencing July 2027. You will gain hands-on experience with submissions, registrations, packaging and product updates under close su...Read More>>.

Regulatory Affairs Associate (VMS /Food Supplements) - 9 Month Maternity Cover – Start November 26 Chippenham, Wiltshire (Hybrid 2 days onsite) At Alliance, we're a fast-growing, science led consumer healthcare business focu...Read More>>.

Boehringer Ingelheim invites motivated students to join a 12-month internship in Regulatory Affairs UK, Ireland and Malta. Based at our Winnersh office, you will contribute to regulatory submissions, document control and cross-functional projects,...Read More>>.

SRG is offering a Regulatory Affairs Early Talent Programme in Maidenhead with a 2-year rotation across Europe Area and UK Affiliate Regulatory Affairs. This role is designed for graduates starting their careers, providing structured development a...Read More>>.

STADA UK Thornton & Ross invites applications for a Regulatory Affairs Placement Student in Huddersfield. This year‑long, full‑time placement offers hands‑on experience supporting submissions, registrations, packaging and product updates und...Read More>>.

Caraway Therapeutics, Inc. is offering a 12-month Regulatory Affairs CMC student placement in London to gain hands-on experience with regulatory strategy, submissions management, and health authority engagement.The role includes exposure to...Read More>>.

Matchtech is assisting a medical device business near Fareham, Hampshire, to recruit a Quality Engineer focused on quality systems, compliance and audits. The role is permanent and hybrid, emphasizing audit readiness, CAPA, and embedded quality pr...Read More>>.

Ernest Gordon Recruitment is seeking a Quality Engineer for a medical devices manufacturer in Andover, Hampshire. The role focuses on maintaining and developing the QMS within a high-end cleanroom and ensuring ISO 9001/13485, AS9100 compliance....Read More>>.

Becton, Dickinson and Company is seeking a Complaints Investigation Engineer to evaluate, investigate, and resolve customer complaints on medical devices. You will perform root cause analyses, testing, and documentation in a regulated environment,...Read More>>.

Tangerine Search is seeking a field-based Medical Devices Sales professional to cover East Midlands, Lincolnshire, and Bedfordshire. You will engage NHS and private sector stakeholders, manage key accounts, and lead contract and pricing negotiatio...Read More>>.

Our client is a fast-growing, well-funded company authorised to assess and certify medical devices, combining clinical, technical and regulatory expertise with modern technology to help ambitious health-tech companies bring safe products to market...Read More>>.

Maple Talent Solutions is seeking a first class Business Development Manager to work in the South Birmingham, Worcestershire and Warwickshire area, joining a high growth medical device business in a strategic sales role.The role involves dr...Read More>>.

Forest Hospitals NHS Foundation Trust invites applications for an Orthotic Technician at King's Mill Hospital. You will join our in-house orthotic manufacturing facility to manufacture and maintain bespoke orthotic devices.We seek a motivat...Read More>>.

Sherwood Forest Hospitals NHS Foundation Trust in Sutton-in-Ashfield is seeking an Orthotic Technician to join our in-house orthotic manufacturing facility. You will manufacture and maintain bespoke devices, with opportunities to develop skills in...Read More>>.

Keeler, a global eyecare leader and Halma member, is based in Windsor and seeks a Technical Support Associate to deliver first-line support for Keeler’s products and software, including Keeler Konnect, Accutome Connect, Kapture and Kinexis....Read More>>.

Company DescriptionWe are SGS – the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 100,000 employees operate a network of 2,600 off...Read More>>.

SGS UK Ltd in the Birmingham area is seeking a Senior Technical Medical Device Coordinator to support the UK Medical Devices Team. You will coordinate Technical Documentation Reviews, monitor KPI reports and drive actions to resolve issues....Read More>>.

Stryker Belfast is seeking a Manufacturing Operator on a permanent basis to help build life-saving medical devices in a quality-focused, supportive environment. This onsite role offers a clear career path within a world-leading medical device comp...Read More>>.