Overview As Director, Regulatory Affairs, Labelling you will lead global labelling strategy for Ipsen’s products across development and lifecycle management. You will shape early labeling input with development teams and ensure USPI, EU l...Read More>>.

Overview In this remote, contract-based role you lead global regulatory strategy and submissions for oncology development programs. You will serve as Global Regulatory Lead, guiding cross-functional teams and aligning with corporate objecti...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>>.

United States Digital Space LLC is seeking a talented Software Engineer Embedded Firmware to join their Crawley office. This role involves designing, implementing, testing, and maintaining firmware for innovative radiation therapy medical devices....Read More>>.

Office of Regulatory Relations, Regional Country Compliance, Vice President, London location_on London, Greater London, England, United Kingdom OUR IMPACT The Office of Regulatory Relations (ORR) protects the firm’s regulatory...Read More>>.

Commercial · Proximie London Office · HybridPartnerships Manager, Medical DevicesProximie is on a mission to improve healthcare by transfor...Read More>>.

Goldman Sachs Bank AG in London is seeking a Senior Analyst for Regulatory Outreach within Client Experience Operations. You will help the firm identify, engage and influence clients through regulatory change, while developing best practices and r...Read More>>.

CoMind develops non-invasive neuromonitoring technology for clinical brain monitoring. Its technology transforms neuro-signals into longitudinal patient insights to improve the diagnosis and treatment of brain disorders.Задачи...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>>.

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>>.

Nuneaton and Bedworth Borough Council is seeking an experienced and dynamic leader to oversee key front-line and enforcement services within a broad portfolio, delivering meaningful outcomes for residents and communities.You will provide st...Read More>>.

Ready to lead global regulatory strategy and influence the development of innovative oncology therapies on a worldwide scale? Proclinical is seeking an Associate Director of Regulatory Affairs to join a dynamic team in the oncology and p...Read More>>.

Director Quality Assurance and Regulatory Affairs This range is provided by Metric Bio. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range Direct message...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>>.

Senior Manager, Regulatory Submission Locations: King of Prussia, PA | Glattburgg, Switzerland | Maidenhead, UKWork Arrangement: Hybrid - 3 days onsiteReports to: Global Submission Management Lead CSL...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>>.

Skills Alliance seeks an SVP Regulatory Affairs / Chief Regulatory Affairs Officer for a leading biotech with a pivotal Phase 3 programme. Lead global regulatory strategy, oversee NDA/MAA submissions and engage with FDA/EMA to drive speed to appro...Read More>>.

Lexington Medical, Inc. in Bedford, Massachusetts, is hiring an Electrical Engineer to design and develop embedded electrical systems for our AEON surgical stapling platform.You will contribute to schematic capture, PCB design, hardware bri...Read More>>.

Baxter International Inc. in the UK, Ireland and Malta seeks a Country Quality Assurance (CQA) & Regulatory Affairs (RA) Manager to lead Quality and Regulatory across the region. Shape regulatory strategies, ensure a robust QMS, and guide cross-fu...Read More>>.

Position DescriptionServe as a Regulatory Chemistry, Manufacturing and Control (CMC) Lead for the synthetic-moiety (Drug-Linker) of assigned antibody-drug conjugate (ADC) and other bio-conjugate programs, providing regulatory lead...Read More>>.

Flusso Limited is seeking a Senior Firmware Engineer to advance firmware for Flusso sensor solutions, typically on ARM-based MCUs or ASIC cores. The role involves developing firmware for sensing applications and supporting new algorithm developmen...Read More>>.

Keeler Ltd, a global eyecare innovator, invites applications for a Technical Support Associate – Products & Software in Windsor. You will deliver first-line technical support for Keeler product range and software, including Keeler Konnect, Accut...Read More>>.

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 medical technology company is seeking an experienced C or C++ developer to join their mul...Read More>>.

Keeler, part of Halma, is seeking a Technical Support Associate – Products & Software to deliver first-line technical support for Keeler’s product range and software, including Konnect, Accutome Connect, Kapture and Kinexis. Ideal for a recent...Read More>>.

ECM Selection (Holdings) Limited seeks an experienced embedded C/C++ developer to join its multi-disciplinary engineering team near Cambridge. The role offers variety, direct client contact, and the chance to impact medical technology used in labs...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>>.

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>>.

TRS Consulting in the United Kingdom is seeking a Medical Devices Technician responsible for setting up and supporting surgical camera systems, inspecting and replacing devices, and providing hands-on clinical support to staff to promote equipment...Read More>>.

Location: Reading (Head Office) Start date: 1st July 2027 Duration: 13 months – Until 31st July 2028 Working Model: Full-time Hybrid position (3 days in office, 2 days working from home) Face to Face Assessment Days: December 2026About t...Read More>>.

National Highways is seeking an Assistant Lawyer to join the Legal Services team. Reporting to the Team Leader within the General Counsel - Legal function, you will provide pragmatic and effective legal advice across a broad range of disciplines,...Read More>>.

Job responsibilities To support the UK Medical Devices Team to ensure that all activities required within the department are completed to the required standards, timescale and meet any internal or contractual KPI. To provid...Read More>>.

The Medical Devices Safety Officer (MDSO) will provide Trust-wide leadership, oversight and assurance in relation to the safe management, governance and regulatory compliance of medical devices across The Walton Centre NHS Foundation Trust. The po...Read More>>.

Pratap Partnership Ltd is seeking a Quality Control Officer - Medical Devices to support the day-to-day operation of the QMS in a hybrid role. You will work closely with the Quality Assurance Manager on QMS coordination, internal audits, CAPA, com...Read More>>.

Johnson & Johnson in Leeds, West Yorkshire seeks an Import/Export Operations Specialist to manage compliant, timely cross-border movement of DePuy Synthes products. You will handle trade docs, customs, and regulatory requirements in a regulated me...Read More>>.

FlexMedical Solutions, a growing medical device development and manufacturing organisation based in Livingston, seeks an experienced Project Manager to own customer programmes from contract through design, development and manufacture. You will coo...Read More>>.

Guided Solutions is supporting an established medical device business expanding its UK commercial team. The NHS Territory Manager role offers a commercially minded sales professional the chance to own a territory and progress within healthcare sal...Read More>>.

Stryker Corporation in the United Kingdom is seeking an Associate Sales Representative to start a career in medical devices. You will work with an experienced team to grow Neuro and Spine business, develop relationships with surgeons and hospital...Read More>>.

Caraway Therapeutics, Inc. in London offers a 24-month Regulatory Affairs Graduate Programme with rotations in International Regulatory Affairs CMC and UK Regulatory Affairs. The role provides exposure to regulatory strategy, submissions, complian...Read More>>.

Johnson & Johnson–DePuy Synthes in Leeds offers a 12-month non-LDP Intern/Co-Op in the Quality/Sterility Assurance area. You’ll work with scientists, engineers and production teams, gaining hands-on experience across the full product lifecycle...Read More>>.

Alliance Pharma PLC in Chippenham, Wiltshire, offers a hybrid Regulatory Affairs Associate role (VMS/Food Supplements) for a 9-month maternity cover starting November 26. The post supports maintenance and development of an EMEA portfolio across VM...Read More>>.

Stryker Belfast is hiring a Manufacturing Operator for the night shift to help build life-saving medical devices in a fast-paced, quality-focused environment. You will work on a production line, assemble, test and package products to meet daily ta...Read More>>.

Manpower UK is seeking a Customer Service Representative for a world-leading healthcare company in Leeds. The role is full-time and hybrid, 37 hours per week, with a two-week rotating schedule and pay starting at £13.85 per hour, rising to £15.0...Read More>>.

BMS Performance Ltd. is seeking a Graduate Account Manager to grow the existing account base in the south of the UK. You will meet customers face-to-face and uncover their needs to deliver respiratory solutions.The role targets NHS and priv...Read More>>.

Matchtech is assisting a medical device business near Fareham, Hampshire, to recruit a Quality Engineer focused on quality systems, compliance and audits. The role is permanent and hybrid, emphasizing audit readiness, CAPA, and embedded quality pr...Read More>>.

Tangerine Search is seeking a field-based Medical Devices Sales professional to cover East Midlands, Lincolnshire, and Bedfordshire. You will engage NHS and private sector stakeholders, manage key accounts, and lead contract and pricing negotiatio...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>>.

Stryker Belfast is seeking a Manufacturing Operator on a permanent basis to help build life-saving medical devices in a quality-focused, supportive environment. This onsite role offers a clear career path within a world-leading medical device comp...Read More>>.