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>>.

Build your career while making a difference in healthcareAt Vitalograph, we've spent more than 60 years developing innovative respiratory diagnostic solutions that help healthcare professionals detec...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>>.

Allucent is seeking a Director of Regulatory Affairs to guide clients through drug, biologic and medical device development. You will lead regulatory teams, shape strategies, and ensure high-quality submissions while Interacting with Health Author...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>>.

GxPeople Global partners with a venture-backed UK medical device company to recruit an experienced R&D Manager for its London-based development programme. The role combines technical ownership across hardware, software and system-level workstreams...Read More>>.

Quality Start in Walsall is seeking a Test Quality Assurance Engineer to design, implement and perform quality tests for medical device software and hardware. You will translate product requirements into test procedures, develop test plans, and be...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>>.

Location Primsdown Industrial Estate, Worcester Road,Chipping Norton, Oxfordshire, OX7 5XP,United Kingdom Employee Type Contractor or FT Employee Required Degree 4 Year Degree Description About EC...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>>.

Location Primsdown Industrial Estate, Worcester Road,Chipping Norton, Oxfordshire, OX7 5XP,United KingdomEmployee Type Contractor or FT EmployeeRequired Degree 4 Year DegreeAbout ECIECI’s mission 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>>.

Under the supervision of line management or guidance from an experienced Senior Regulatory Manager, conduct agreed strategic regulatory activities for assigned products and markets to obtain and maintain Marketing Authorizations and support Clinic...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>>.

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>>.

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>>.

Hologic in Cambridge is seeking a Senior Regulatory Affairs Specialist to support regulatory submissions, audits, inspections, and lifecycle activities for medical devices across US, EU, and Canada.You will work cross-functionally with Regu...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>>.

Rayner is seeking a Territory Manager in the London area to lead sales performance across ophthalmic products. You will develop territory plans, build relationships with surgeons and hospital stakeholders, and deliver product demonstrations....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>>.

Convatec is relocating the majority of its UK R&D activities from Deeside to Manchester from late 2027/early 2028, expanding facilities and creating a new global testing hub. The Senior Technical Project Manager will drive cross-functional NPD and...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>>.

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>>.

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>>.

Steris is seeking a Systems Engineer within the Infection Prevention Technology (IPT) division. The role focuses on technical leadership, translating stakeholder requirements into system level designs, and leading cross-discipline feasibility and...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>>.

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>>.

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>>.

Stryker is hiring an Enterprise Accounts Manager for private groups across the UK. This field-based role focuses on developing strategic relationships with major healthcare accounts, managing contracts, and driving cross-divisional growth.K...Read More>>.

Johnson & Johnson’s DePuy Synthes Trauma team seeks a Sales Specialist to cover the London North & East England region, including Mid & South Essex and East Hertfordshire. You will drive trauma and extremities product sales, build key relationsh...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>>.

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>>.