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 Join Moody’s Government, Public and Regulatory Affairs to guide insurance regulatory strategy across EMEA. You will shape policy positions, engage with regulators, and apply AI-driven approaches to improve regulatory workflows. T...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 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 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>>.

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>>.

Regulatory Affairs Advisor – Hybrid To c£45,000 + package Worcester, Redditch, Evesham, Warwick, Cheltenham, Tewkesbury, Droitwich Spa, region around WR11.This business is an international leader in manufacturing and raw material...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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

United States Digital Space LLC is seeking a Medical Device Auditor to audit manufacturers’ quality management systems against ISO 13485, EU MDR and UK MDR. You will learn our audit methods and deliver clear conclusions to support certification...Read More>>.

Monitor FCA, PRA and SRA AI regulatory developments and translate them into product requirements for Trovix Watch and Audit. You will work closely with a team of engineers, domain experts and regulated industry clients to deliver AI products th...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>>.

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>>.

1 week ago Be among the first 25 applicantsGet AI-powered advice on this job and more exclusive features.Direct message the job poster from Entrust Resource SolutionsFinding Outstanding Talent in the Emerging Scientific Indus...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>>.

Revolut is seeking an experienced Regulatory Affairs Manager to lead interactions with external regulators and ensure ongoing compliance as the company expands its regulated fintech operations. You will translate complex regulatory proposals into...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>>.

Pfizer Inc. is seeking a Senior Regulatory Manager to drive regulatory strategy for assigned products and markets. You will partner with cross-functional teams to obtain and maintain marketing authorizations and support clinical trial applications...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>>.

OrganOx Limited is seeking a Senior IP Specialist to define and execute the company’s global IP strategy. The role acts as the internal authority on IP matters and collaborates with R&D, regulatory, and business teams to protect and exploit the...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>>.

Newton Colmore Consulting in Cambridge is seeking an embedded software engineer to work on diagnostics technologies for the Medical Devices and Life Sciences sectors. The role is permanent and full-time, with an excellent starting salary and compr...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>>.

ECM Selection (Holdings) Limited seeks an experienced embedded C/C++ developer to join a multidisciplinary engineering team. You will work on medical technology projects, from on-board device software to driven hardware interfaces, with direct cli...Read More>>.

Product Security Specialist for Medical Devices (Cyber Security) We believe in the power of ingenuity to build a positive human future. As strategies, technologies, and innovation collide, we create opportunity from complexity....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>>.

OrganOx is seeking a Windows Software Manager to lead the design and development of device-hosted software for Windows platforms, ensuring quality, regulatory compliance, and robust GUI/connectivity features for NMP-based organ management solution...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>>.

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>>.

Corin Group is seeking a Senior Software Quality Engineer to oversee software and system development activities across its Global Technology Team. You will ensure compliance with FDA, ISO, and European Medical Device standards and drive quality im...Read More>>.

Bluetree Recruits is seeking a Senior Regulatory Affairs & Quality Manager in Cambridge to shape regulatory strategy for the US first and expand globally. You will own FDA, CE and UKCA submissions and lead a robust QMS, partnering with leadership...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>>.

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>>.