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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

Zenopa is seeking an experienced Territory Manager to drive sales growth and provide clinical support across a specialist surgical portfolio in the UK. The role focuses on minimally invasive surgery, with in-theatre support, product training and r...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>>.

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>>.