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>>.

Field Service Engineer, Medical Devices Basic Salary £45,000 to £50,000Pension Company Vehicle Private Medical Cover...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 support the development and continuous improvement of the Quality Management System within a growing medical device business near Fareham. You will help maintain audit readiness, support regulatory compliance,...Read More>>.

Overview In this Senior Development Engineer role you will translate concepts into validated medical device solutions. You will work on complex devices from early concept through testing, shaping innovative technologies that improve lives....Read More>>.

Overview In this global role, you shape regulatory readiness and policy positions to support responsible innovation and growth in a data-driven tech environment. You’ll scan regulatory developments, distill implications for the business,...Read More>>.

Arevna Cambridge, England, United KingdomRegulatory Affairs Manager (IVD)Arevna Cambridge, England, United Kingdom2 days ago Be among the first 25 applicantsDirect message the job poster from ArevnaOverview...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>>.

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to...Read More>>.

Roche is seeking a Principal for Medical Device safety operations to lead end-to-end case processing and process design across the global network. You will own post-market incident reporting and pre-market clinical investigation safety reporting,...Read More>>.

AbbVie in Maidenhead seeks a senior Regulatory Affairs professional to lead UK regulatory efforts and serve as primary regulatory contact for designated therapeutic areas, guiding MHRA submissions and supporting launches. The role aligns with the...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>>.

Global Innovation and Technology Centre, Back Lane, Melbourn, Hertfordshire, SG8 6DP, United Kingdom, Melbourn SG8 6DP, GBPA works with many of the world’s most innovative pharmaceutical, medical device and life sciences companies. Bas...Read More>>.

OverviewProduct Quality Engineer – Medical DevicesLocation: KidlingtonSalary: Highly Negotiable, Dependent on ExperienceAn exciting opportunity to join a growing...Read More>>.

Medical Device Regulatory and Quality Consultant We are seeking a highly skilled consultant with experience in medical device and/or combination product Quality and Regulatory processes to join our Healthcare & Life Sciences (HLS) cons...Read More>>.

Regulatory and Scientific Affairs Senior Manager | Leatherhead Food Research Department: Regulatory Employment Type: Permanent - Full Time Location: Epsom Description We are looking fo...Read More>>.

CoMind, based in Greater London, is seeking a Staff Software Engineer to join their innovative software team. You will be responsible for leading technical challenges in embedded C++ development and ensuring high-performance software for clinical...Read More>>.

Elekta in Crawley is seeking a Senior Software Development Engineer to advance cutting‑edge workflow, delivery and imaging software for radiotherapy systems. You’ll work in a safety‑critical environment where software quality is paramount an...Read More>>.

United States Digital Space LLC is seeking a Software Safety Engineer to assess software lifecycle processes and regulatory documentation for medical device software. You’ll work with our product, engineering and applied machine learning teams t...Read More>>.

Leatherhead Food Research is seeking an experienced Regulatory and Scientific Affairs Senior Manager to lead high-impact regulatory projects for global food and beverage clients. The role combines regulatory expertise with project leadership and p...Read More>>.

AND Digital is seeking four Embedded C++ Developers for an in-house backend engineering team working on a highly regulated medical technology product in London. You will own a self-contained area of the application and drive design through to test...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>>.

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>>.

About the Role We are seeking an experienced and results-driven Manager, Medical Devices Service Centre to lead a critical service operation supporting our medical device portfolio. This role is responsible for delivering exceptional o...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>>.

AtriCure, Inc. is seeking a Regional Sales Manager to prospect, qualify, and close direct business in cardiac operating and related departments within hospitals. You will train and support the surgeon and staff in procedures and provide in‑O.R....Read More>>.

AND Digital Limited is seeking four Embedded C++ Developers to join an in-house backend team on a highly regulated medical technology product in London. You will own a self-contained area of the application from design through tested, documented c...Read More>>.

Leo Cancer Care is seeking a Mechanical Engineering Lead to drive robust, safe, and manufacturable designs for cancer treatment equipment. You will lead a small team within a regulated environment, coordinating with electronics, systems, software,...Read More>>.

Moody's is seeking an Assistant Vice President for UK Government and Public Affairs to drive engagement with government, regulators, and industry stakeholders. The role emphasizes policy development, regulatory insight, and cross-functional collab...Read More>>.

Vertech Group (UK) Ltd in London is seeking a Safety Software Engineer to join a team evaluating software development processes and technical evidence underpinning AI-enabled medical devices. You will review software lifecycle, V&V, configuration...Read More>>.

Integra LifeSciences is seeking a Clinical Specialist to support account managers across London, Brighton and Hampshire. You will train customers, conduct educational workshops, and provide in-theatre product support post-sale to drive business gr...Read More>>.

An exciting opportunity for an experienced Regulatory Affairs Manager to take on a new role in a growing generic pharmaceutical company working towards a portfolio of 220 licenses. ++ Please note that this role will be onsite 5 days per...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>>.

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>>.

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>>.

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>>.

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>>.

Stryker is recruiting an Enterprise Accounts Manager for UK Private Groups to manage and grow high-value accounts across the private sector. This field-based role focuses on relationship-building with C-Suite, procurement, and supply chain stakeho...Read More>>.

Albus Health in Oxford is seeking a senior medical-device verification engineer for an initial three-month contract with potential extension. You will strengthen verification evidence and regulatory documentation for FDA submissions.You wil...Read More>>.

About Albus HealthAlbus Health is an Oxford University spin-out transforming how health data is collected and used in clinical trials and drug development.We have developed Albus Home, a contactless multisensory platform that conti...Read More>>.

CMR Surgical Ltd. is seeking a procurement leader to manage supplier relationships and optimise the sourcing function. The role supports the Versius robotic system, with a hybrid work model requiring 3 days in the Ely/Cambridge office, and global...Read More>>.

About Albus Health Albus Health is an Oxford University spin-out transforming how health data is collected and used in clinical trials and drug development. We have developed Albus Home, a contactless multisensory platform that con...Read More>>.

Siemens Healthineers seeks a maintenance engineering leader to direct an engineering team responsible for maintaining medical device manufacturing equipment. You will set day-to-day priorities, manage workload, and ensure high performance across m...Read More>>.

BSI is seeking a Western EMEA Sales Manager to lead our Regulatory Services (Medical Devices) commercial team across the UK and EMEA. This homebased role shapes regional sales strategy and develops a high-performing team to deliver ambitious growt...Read More>>.

Guided Solutions is seeking an experienced Global Product Manager to shape strategy for a global portfolio spanning hardware and software medical devices. You will lead the roadmap, translate insights into product direction, and collaborate with r...Read More>>.