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>>.

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>>.

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>>.

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>>.

Location: Hybrid role, with ideally a few days each week spent at Head Office, in Selby, North Yorkshire Department: Research & Development/Quality Join GBUK and help deliver medical devices that make a difference....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>>.

Ernest Gordon Recruitment is seeking a CNC Programmer for a medical manufacturing role in Redhill, Surrey. You will code and edit CNC programs, test new programs and set, operate and troubleshoot CNC machinery, ensuring documentation is precise....Read More>>.

An exciting opportunity has arisen within this leading manufacturer of medical devices into the global healthcare and Pharmaceutical industries for a Field Service Engineer to be based in the Crewe, Stoke on Trent, Newcastle under lyme, Stone,...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>>.

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>>.

Abbott Laboratories in Sittingbourne, United Kingdom, is seeking a Manager for the Medical Devices Service Centre to direct a multi-disciplinary team of up to 30 people. This leadership role focuses on delivering exceptional service, quality, comp...Read More>>.

Abbott is recruiting for a Field Service Engineer/Junior based in Peterborough/Leicestershire/Northampton area, with flexibility to travel to Ireland, Nordics and Poland. You will install, upgrade, repair and perform preventive maintenance of vasc...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>>.

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>>.

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>>.

Pure Search partners with an established international financial services business to appoint Head of Compliance & Regulatory Affairs – British Isles. Based in Jersey, you will oversee regulatory compliance and financial crime frameworks across...Read More>>.

We Are The People Who Give Possibilities PurposeBD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passio...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>>.

Moody's in London seeks an AVP, EMEA Regulatory Affairs to support regulatory strategy across the EMEA region through stakeholder engagement, thought leadership, and cross‑functional collaboration.The role manages relationships with regul...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>>.

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>>.

Develop embedded C and C++ software to bring new medical technology to lifeLooking 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 medic...Read More>>.

We’re looking for an experienced Windows Software Engineer with a background in medical devices and IoT to join a growing engineering team.This is an exciting opportunity for a software engineer who enjoys working on complex...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>>.

OrganOx is seeking an Electronics Design Engineer to design, develop and support electronics for medical devices. The role covers full lifecycle from concept through manufacturing handover, with emphasis on regulation and safety compliance....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>>.

CamWebDir in Otley, UK is seeking an enthusiastic embedded software engineer to contribute to medical device development. You will work hands-on across the software lifecycle, writing robust C/C++ code and ensuring documentation is clear and thoro...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>>.

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>>.

STADA UK Thornton & Ross is on an exciting growth journey with more than 700 employees being fully committed to our purpose of Caring for People’s Health as a Trusted Partner. Together we are shaping the future of Thornton & Ross by living our v...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>>.

Our client, an innovative medical device business based near Fareham in Hampshire, is seeking a Quality Engineer to support the development and continuous improvement of its Quality Management System. Working within a growing medical technolo...Read More>>.

Vertage Group Portfolio is offering an Regulatory Affairs Early Talent programme in the UK. This two-year rotation spans UK Affiliate Regulatory Affairs and Europe Area Regulatory Strategy, designed to accelerate development for graduates starting...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>>.

Programme Eligibility To join one of our 12-month Internships you must meet one of the following criteria: You’re currently an undergraduate studying at University and returning to full time education in Autumn 2028...Read More>>.

Stryker Belfast is seeking a Manufacturing Operator for a permanent role. You will help build life-saving medical devices, stay compliant with quality standards, and contribute to a supportive, development‑focused environment.You will joi...Read More>>.

Role Summary 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 al...Read More>>.

Adore Recruitment Ltd is recruiting a Territory Sales Manager to cover the North UK for a growing international medical devices manufacturer. You will leverage healthcare knowledge to develop new business, demonstrate devices and build long-term r...Read More>>.

Kleboe Jardine Ltd in Edinburgh is seeking a Product Design Engineer to lead design and development of medical devices from concept to production, blending practical engineering with healthcare applications.You will work closely with engine...Read More>>.

Medtronic in London is seeking a field-based medical device sales specialist to grow the Operating Room Essentials portfolio across London and the South East. You will manage territory planning, lead product conversions, and engage NHS and private...Read More>>.

Stryker is seeking an Associate Sales Representative in the UK to start a career in medical devices. You will maintain existing business and identify new sales opportunities in Neuro and Spine, while building relationships with surgeons and hospit...Read More>>.

Trulife in the United Kingdom seeks an Inside Sales Executive to drive sales growth through proactive telephone and digital engagement with NHS, private healthcare, mobility, orthotics and distributor customers from their Sheffield base.You...Read More>>.