Overview You lead a global Medicines Lifecycle Management team to deliver post-approval regulatory strategy and ensure compliant, timely submissions across a diverse portfolio. You translate regulatory needs into practical plans, partnering...Read More>>.

Overview As Director of Structured Content Authoring, you will lead the move from document-centric regulatory operations to a data-driven, component-based model. You’ll set vision, governance and a roadmap that links regulatory content, m...Read More>>.

Overview In this role you will help invent life-changing medical devices from Cambridge, collaborating with physicists, engineers and industry experts. You’ll work across imaging, surgical systems, electro-medical and other complex techno...Read More>>.

Overview In this role you lead Perrigo's global Regulatory Affairs Lifecycle Management for Medicines, shaping strategies across the full product lifecycle. You will drive end-to-end dossier development, submissions, and maintenance to meet...Read More>>.

Overview In this role, you will lead regulatory activities for Galderma’s medicinal products across the UK and Ireland, ensuring regulatory compliance and lifecycle management. You will shape local regulatory strategy in partnership with...Read More>>.

Overview In this role, you will assess and improve quality management systems for software-based medical devices, ensuring regulatory compliance and robust processes. You’ll work within a cross-functional context to strengthen QMS and sup...Read More>>.

Overview In this role you lead drug delivery and combination product programmes from concept to industrialisation within PA’s life sciences practice. You provide senior technical leadership across engineering, usability, risk and manufact...Read More>>.

Overview In this role you will help invent and improve Medical Devices within a collaborative, multi-disciplinary environment in Cambridge. You’ll translate inventive ideas into practical devices across drug delivery, diagnostics, wearabl...Read More>>.

Overview In this role you will lead international CMC regulatory activities to support global product development. You’ll manage agency communications, ensure quality CMC sections, and influence submissions across multiple programs. You w...Read More>>.

Overview In this role, you shape and execute the Global Regulatory Affairs strategy for the IVD and life sciences portfolio, guiding regulatory pathways and milestones across the product lifecycle. You will lead regulatory submissions with...Read More>>.

Overview In this role you contribute to EU regulatory strategies for Amgen’s biosimilar portfolio, guiding submissions from development to launch and lifecycle management. You will collaborate with global and regional teams to prepare MAA...Read More>>.

Overview In this role you will lead UK regulatory strategy and the RA team to secure and maintain marketing authorizations for programs across development, registration, and lifecycle. You will coordinate with cross‑functional stakeholder...Read More>>.

Overview In this role you will drive the design and development of innovative medical devices within a multidisciplinary team. You will turn concept ideas into robust, manufacturable hardware through hands-on mechatronics work. You’ll col...Read More>>.

Regulatory Affairs Manager page is loadedRegulatory Affairs ManagerApply locations UK - High Wycombe, Buckinghamshire time type Full time posted on Posted 30+ Days Ago job requisition id JR100567Reporting into the Head of Te...Read More>>.

Head of Regulatory Affairs – UK & Ireland An outstanding opportunity has arisen within a leading, innovation-driven pharmaceutical company dedicated to delivering value-based, patient-centric healthcare solutions. As Head of Regulato...Read More>>.

Department: Vicon Quality & Regulatory Compliance Location: Yarnton, Oxfordshire Description Are you interested in working on products at the very cutting edge of technology? Want to join Vicon, an Academy Award®-winning...Read More>>.

Regulatory Affairs Director Our client is a young, exciting publicly listed clinical‑stage company dedicated to transforming the lives of patients in its therapy areas. With its novel and proprietary drug products and current clinica...Read More>>.

CY Partners are excited to be supporting a global organisation in recruiting an enthusiastic, scientifically minded scientist to join their experienced regulatory team. This is an excellent opportunity to work in chemical regulatory affairs, wo...Read More>>.

Contract: Full-time, Permanent Are you ready to make a difference in the beauty industry? Join us at Boots as a Regulatory Manager within the No7 Beauty Company’s Research & Development team in Nottingham! At Boots, we wo...Read More>>.

Export Control and regulatory Coordinator Location: Swinton, ManchesterDepartment: Quality & ComplianceSalary: £32,000 – £40,000 per annum About Luxfer Luxfer MEL Technologies is a lea...Read More>>.

Job Title: Regulatory Affairs Director Location: Cambridge Salary Competitive Introduction to role: Are you ready to shape European regulatory strategy that accelerates innovative oncology medi...Read More>>.

Regulatory Affairs Specialist We’re looking for a Regulatory Affairs Specialist to join us, working across multidisciplinary teams to support and enable breakthrough innovation. Cambridge Consultants is a global technology and...Read More>>.

The Regulatory Affairs (RA) Officer is primarily responsible for ensuring the appropriate licensing, marketing and legal compliance of Sun Pharma’s pharmaceutical and medical products in order to control the safety and efficacy of these produ...Read More>>.

Flexi Start Happy Hour Drinks Fridge (Thursdays & Fridays) #TEAMBULK ARE HIRING A REGULATORY AFFAIRS ASSOCIATE Bulk™ is on an incredible journey, with a mission to move the business from a manufacturi...Read More>>.

TOGL(Holdings)Limited is a diagnostics company focused on diseases of the gastrointestinal tract. Our current research and validation programme targets accurate and efficient triage of patients with symptoms of colorectal cancer (CRC). We are l...Read More>>.

KG MedTech Recruitment Specialists are partnering with a medical device CDMO in Thornaby to recruit a hands-on Project Engineer. You will oversee projects from initial enquiry through to production, setting up BOMs, materials planning, subcontract...Read More>>.

SRG Cambridge is seeking a Senior Design Assurance Engineer to join a medical device organisation focused on next-generation drug delivery devices and combination products.You will provide design assurance across the product development lif...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>>.

Barrington James is seeking a Software Safety Engineer in London, operating in a hybrid setup with 3–4 days in the office. You will assess medical device software safety, review lifecycle processes and evidence, and support certification decisio...Read More>>.

Flusso Ltd. seeks a Senior Firmware Engineer to develop real-time firmware for ARM-based microcontrollers and ASIC cores, and to port firmware to new processors. The role supports sensor products, evaluation kits, and PC interfaces, with a strong...Read More>>.

Newton Colmore Consulting is working with a medical devices company based in Cambridgeshire to recruit a Mechatronics Design Expert to lead the design of next-generation machines. This role offers the chance to work on cutting-edge medical technol...Read More>>.

Corin is seeking a motivated individual to join our Quality Control team as a Quality Inspector Assistant in Cirencester. This entry-level role offers comprehensive training to develop into a full Quality Inspector, with exposure to product inspec...Read More>>.

Platform Recruitment in Cambridge is seeking a hands-on Senior Mechanical Engineer to join an innovative medical devices company. You will lead the development of precision mechanical systems for drug delivery products, taking designs from early c...Read More>>.

JOB DESCRIPTION: 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 exceptio...Read More>>.

Medtronic Digital Technologies is seeking a Senior Software Engineer to advance intra-operating device software using modern C++ (C++17+), across embedded, application, and cloud teams. You will own maintainability and help build the software stac...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>>.

CIBSE Journal in Cambridgeshire is seeking a Senior Mechanical Engineer to design and develop advanced electro–mechanical medical devices. This role is hybrid and offers opportunities to work on cutting‑edge products that improve lives....Read More>>.

Medtronic is seeking a Software Development Engineer in Test to design and build automated test solutions for device software, firmware, and hardware-software interfaces. You will work with embedded and edge technologies, including Android/Linux,...Read More>>.

Zenovo is seeking an Embedded Software Engineer in Cambridge to develop software for medical devices. You will work on real-time control, sensor data handling and hardware integration in a collaborative engineering environment.The role focu...Read More>>.

The Stryker Group in Belfast offers a placement within the Regulatory Affairs & Compliance Engineering team. You will gain hands-on experience supporting product registrations, change management, and Eudamed documentation, while collaborating with...Read More>>.

SRG is seeking a motivated Quality Engineer to maintain and improve the Quality Management System (QMS) for medical devices and ensure compliance with ISO 13485, MDR/EU guidance, and customer requirements. You will collaborate with internal teams...Read More>>.

Medtronic in the United Kingdom is seeking a Field Service Engineer to support customers across Manchester and the surrounding region. You will provide installation, maintenance, troubleshooting, and repair of a diverse portfolio of medical techno...Read More>>.

Medtronic plc in Watford, United Kingdom, is seeking a Field Service Engineer to provide installation, maintenance, troubleshooting, and repair of medical equipment across the assigned territory, with 50–75% travel. You will partner with hospita...Read More>>.

Abbott Witney is seeking multi-skilled Support Engineers to join our Operations Group, performing preventive maintenance, responding to breakdowns and monitoring equipment performance. You will support projects to improve yields and efficiencies i...Read More>>.

Stryker Corporation is seeking a motivated sales professional to lead the Joint Replacement and Robotics business in the Greater Manchester area. You will develop territory strategies, deliver sales targets, and build strong NHS and private sector...Read More>>.

Roche in Welwyn Garden City, UK offers a two-year One PDR ET Program to build foundational regulatory experience across the product lifecycle. You will collaborate with global teams, supporting regulatory documents and Health Authority interaction...Read More>>.

Stryker Belfast is seeking a Manufacturing Operator to assemble, test and package life‑saving medical devices on a busy production line. You will follow defined work instructions, balance speed with accuracy and help maintain safety and quality...Read More>>.

Stryker Foot & Ankle is seeking a high-performing sales professional to drive growth across Yorkshire. You will meet and exceed sales objectives, represent Stryker as a market leader, and build strong relationships with surgeons and HCPs.Th...Read More>>.

Carbon 60, Inc. is seeking a Scientist I - Physical Testing to support the development of medical devices in a fully on-site role in Deeside. The position focuses on conducting physical tests, data generation and analysis to GMP/GLP/GDP standards,...Read More>>.