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>>.

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>>.

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>>.

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>>.

Parexel is seeking an experienced Regulatory Affairs Consultant CMC Author to support our client. The role focuses on CMC authoring for initial submissions and lifecycle management, with emphasis on biologics.The position can be home or off...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>>.

GBUK is seeking a Validation Engineer to join its R&D and Quality teams in a hybrid role with the head office in Selby, North Yorkshire. You will lead validation activities across the product lifecycle, ensuring safety, quality and regulatory comp...Read More>>.

Morgan McKinley (South West) in Bristol is seeking a Senior Electronics Engineer to lead design and system architecture for medical-grade computing devices, driving electronic subsystems and mentoring a hardware team.You will own analogue/d...Read More>>.

eg technology is seeking a seasoned Project Manager to lead planning, control and delivery of complex product design and development projects from concept to manufacture. You’ll work with clients and motivate multidisciplinary teams across softw...Read More>>.

Redshore, a leading manufacturer of medical devices, is seeking a Field Service Engineer to cover Stoke-on-Trent, Crewe, Stafford, Congleton and surrounding areas. You will service and maintain a range of electro-mechanical equipment in medical en...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>>.

The Senior Manager, Regulatory Affairs will work with EU regulatory lead(s) and/or directly with global regulatory lead(s) and within cross‑functional teams to facilitate submission of applications to EU and International health agencies (HA)...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 in...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>>.

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>>.

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>>.

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>>.

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>>.

Moody's AVP, EMEA Regulatory Affairs leads policy engagement across regulators and governments, shaping regulatory thinking and strategy across the region. You will produce briefing materials, represent Moody's at key industry events, and drive cr...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>>.

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>>.

Senior Regulatory Affairs & Quality Manager - Cambridge, Cambridgeshire Are you the person regulators, notified bodies and leadership teams turn to when the answer really matters? Bluetree are working with an innovative cardiology me...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>>.

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>>.

BD is seeking a Regulatory Affairs professional to manage regulatory activities for combination devices and pharmaceuticals. You will lead NDA/ANDA/PAS/CBE submissions, interact with FDA CDER, and drive regulatory strategies across R&D, Quality, M...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>>.

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>>.

Amgen Inc. in the United Kingdom (Uxbridge/Cambridge hybrid) seeks an EU Regulatory Affairs Manager to lead submissions for clinical trials and marketed products.You will craft regional regulatory strategies, provide guidance for regulatory...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>>.

Skills Alliance seeks an experienced Windows Software Engineer to join our growing engineering team in the life sciences / medical technology sector. The role involves designing, developing and integrating Windows-based software components across...Read More>>.

Scarlet, a London-based leader in medical-device certification software, is seeking a Product Designer to turn complex regulatory work into clear, efficient experiences. You’ll own core workflows, prototypes and interfaces, partnering with produ...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>>.

UCB is seeking a senior professional to lead human factors and usability activities for drug delivery technologies, medical devices and combination products. You will coordinate global studies, shape patient-centered product improvements and suppo...Read More>>.

Vickerstock are working in partnership with a specialist manufacturing organisation on the appointment of a Group Compliance Officer, based in Co. Fermanagh. Reporting to the SHEQ...Read More>>.