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 As Regulatory Affairs Lead, you will shape and strengthen our regulatory affairs function for a leading trading and reporting consultancy. You will drive engagement with regulators and market participants across UK, EU, and other j...Read More>>.

Overview In this role you guide clients through drug, biologic, and medical device development, leading regulatory teams and shaping strategy to deliver high-quality submissions. You’ll be the trusted HA liaison and translate complex requ...Read More>>.

Overview As Regulatory Affairs Lawyer at Teya, you steer UK and EU licensing, public policy, and regulatory strategy to support independent local businesses. You’ll lead licensing activities, engage with regulators and policymakers, and s...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>>.

Commercial · Proximie London Office · HybridPartnerships Manager, Medical DevicesProximie is on a mission to improve healthcare by transfor...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>>.

CoMind develops non-invasive neuromonitoring technology for clinical brain monitoring. Its technology transforms neuro-signals into longitudinal patient insights to improve the diagnosis and treatment of brain disorders.Задачи...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>>.

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>>.

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>>.

Senior Manager, Regulatory Submission Locations: King of Prussia, PA | Glattburgg, Switzerland | Maidenhead, UKWork Arrangement: Hybrid - 3 days onsiteReports to: Global Submission Management Lead CSL...Read More>>.

At Moody's, we unite the brightest minds to turn today’s risks into tomorrow’s opportunities. We do this by striving to create an inclusive environment where everyone feels welcome to be who they are—with the freedom to exchange ideas, think...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>>.

Baxter International Inc. in the UK, Ireland and Malta seeks a Country Quality Assurance (CQA) & Regulatory Affairs (RA) Manager to lead Quality and Regulatory across the region. Shape regulatory strategies, ensure a robust QMS, and guide cross-fu...Read More>>.

Position DescriptionServe as a Regulatory Chemistry, Manufacturing and Control (CMC) Lead for the synthetic-moiety (Drug-Linker) of assigned antibody-drug conjugate (ADC) and other bio-conjugate programs, providing regulatory lead...Read More>>.

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 medical technology company is seeking an experienced C or C++ developer to join their mul...Read More>>.

ECM Selection (Holdings) Limited seeks an experienced embedded C/C++ developer to join its multi-disciplinary engineering team near Cambridge. The role offers variety, direct client contact, and the chance to impact medical technology used in labs...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>>.

Location: Reading (Head Office) Start date: 1st July 2027 Duration: 13 months – Until 31st July 2028 Working Model: Full-time Hybrid position (3 days in office, 2 days working from home) Face to Face Assessment Days: December 2026About t...Read More>>.

National Highways is seeking an Assistant Lawyer to join the Legal Services team. Reporting to the Team Leader within the General Counsel - Legal function, you will provide pragmatic and effective legal advice across a broad range of disciplines,...Read More>>.

The Medical Devices Safety Officer (MDSO) will provide Trust-wide leadership, oversight and assurance in relation to the safe management, governance and regulatory compliance of medical devices across The Walton Centre NHS Foundation Trust. The po...Read More>>.

Pratap Partnership Ltd is seeking a Quality Control Officer - Medical Devices to support the day-to-day operation of the QMS in a hybrid role. You will work closely with the Quality Assurance Manager on QMS coordination, internal audits, CAPA, com...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>>.

FlexMedical Solutions, a growing medical device development and manufacturing organisation based in Livingston, seeks an experienced Project Manager to own customer programmes from contract through design, development and manufacture. You will coo...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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.