Cure Talent are delighted to be partnered with a growing medical device certification organisation that is expanding its UK audit team. With continued growth in demand, the business is now looking to appoint a Medical Device Auditor to support man...Read More>>.

Global Labelling Lead, Regulatory Affairs, hybrid working, contract jobYour new company We are currently seeking an experienced Global Labelling Lead to join a leading global biopharmaceutical organisation on a contract basis. This is an e...Read More>>.

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>>.

My client is seeking a Regulatory Affairs Associate to join their Global Markets team on a temporary contract basis, supporting regulatory compliance and product registrations across Europe, the Middle East and Africa (EMEA)....Read More>>.

Build your career while making a difference in healthcareAt Vitalograph, weve spent more than 60 years developing innovative respiratory diagnostic solutions that help healthcare professionals detect...Read More>>.

At Elanco (NYSE: ELAN) – it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by o...Read More>>.

12-month fixed-term contract | Hybrid - London Company description Mitra Bio has developed a non-invasive skin sampling that can detect molecular changes in the skin non-invasively. The Company has been awarded the presti...Read More>>.

Galderma Limited (UK) is seeking a Regulatory Affairs Manager for the UK & Ireland, based in London. The role leads local regulatory activities for medicinal products, medical devices and cosmetics where applicable, ensuring compliance, registrati...Read More>>.

Corza Medical is seeking a Graduate Manufacturing Engineer to join our manufacturing team in Taunton. You will support validation, optimization, and continuous improvement of processes in a regulated medical device environment (ISO 13485 and FDA),...Read More>>.

Corin Group in Cirencester is seeking a Senior Quality Engineer (QA) to drive quality excellence in a highly regulated medical devices environment.You will apply FDA, ISO and MDR standards, lead investigations, improve processes and partner...Read More>>.

Company Description About AbbVie AbbVie'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 remarkabl...Read More>>.

HSBC in London is seeking an HCIB Regulatory Affairs Senior Manager to oversee regulatory engagements and developments within MSS. The role is hybrid, based in London, with a comprehensive pay and benefits package and a focus on regulatory change...Read More>>.

HCIB Regulatory Affairs Senior Manager (MSS) Location: London, GB, E14 5HQ Brand: HSBC Area of Interest: Risk and Compliance Role Workstyle: Hybrid Worker Date: 3 Oct 2026 If you’re looking for a caree...Read More>>.

AbbVie seeks an experienced International Regulatory Affairs professional to provide position and guidance on advertising and promotion. You will collaborate with Commercial, Medical, Legal, and Compliance teams to ensure compliant, effective comm...Read More>>.

The role reports to the Head of Materials Compliance, supporting the delivery of the broader EMEA regulatory vision and the mitigation of regional legal risks. The Regulatory Affairs Manager leads the application of the regulatory requirements for...Read More>>.

IQVIA is seeking a MedTech Field Service Engineer Technician to install hardware for automated dispensing systems in healthcare facilities. The role combines hands-on electronics with customer-facing responsibilities and requires travel.You...Read More>>.

If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global coll...Read More>>.

OverviewAt BioTalent, we are working with a client exclusively to fill their RA Specialist position. They are a fast growing CGT company focused on developing products in the immuno-oncology. This role will focus on supporting their exist...Read More>>.

Huntleigh Healthcare Limited in Cardiff is seeking an Electronics Design Manager to lead a dynamic team of medical device design engineers. You will drive multi-disciplinary product development and maintenance, shaping next‑generation electronic...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>>.

W Talent are delighted to be partnering with an established manufacturing business to recruit a Regulatory Affairs Specialist. This is an opportunity to join a growing Technical function, supporting regulatory compliance and ensuring products m...Read More>>.

Job DescriptionRegulatory Affairs SpecialistLocation: Hybrid – Kent/LondonJob Type: Full-time, PermanentAbout the RoleAn exciting opportunity has arisen for a Regulatory Affairs...Read More>>.

Clearline Recruitment Ltd in Motherwell, Scotland, onsite, is seeking a Product Definition Lead for a 12-month contract. You will lead the product definition of technically complex point-of-care systems across instrument, assay and disposable deve...Read More>>.

Arxada is looking for a Regulatory Affairs Specialist based in Manchester, UK. This part-time position offers a hybrid working model and involves delivering regulatory aspects of critical projects, managing post-submission activities, and providin...Read More>>.

Gold Group Limited in London (West W6) is seeking a Human Factors Consultant to join our team, helping design medical device products, services, and experiences that are safe and intuitive within the healthcare sector.You will work with res...Read More>>.

Merck seeks a Principal Scientist to lead a Human Factors team, applying expertise to a broad range of devices across the lifecycle. You will mentor scientists, create HF plans, and coordinate with cross-functional partners to ensure regulatory co...Read More>>.

Job Description The Director, Structured Content Authoring is a transformational leadership role responsible for accelerating the organisation's evolution from document-centric regulatory operations to a modern, data-driven and compon...Read More>>.

CoMind is building non-invasive neuromonitoring tech and seeks a Director of Quality Assurance to shape the QMS, design and supplier quality across electronics, optics and software. You will write procedures, lead audits, and work closely with eng...Read More>>.

General Summary: The Senior Director, Regulatory Strategy International, is a regulatory leader with expert technical and tactical experience in regulatory strategy who will be responsible for overseeing the development and implementat...Read More>>.

CoMind is building a non-invasive neuromonitoring technology to advance clinical brain care. The Software team spans embedded, GUI, ML, and DevOps in a regulated medical device setting.This leadership role guides the product software stack,...Read More>>.

At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a top 10 player in the European Consumer Self‑Care market and the largest U.S. store‑...Read More>>.

At Moody's, we unite the brightest minds to turn today's risks into tomorrow's opportunities. We do this by striving to create an inclusive environment where everyone feels welcome to be who they are-with the freedom to exchange ideas, think in...Read More>>.

CoMind is seeking a Director of Quality Assurance in the United Kingdom to lead QA across QMS, design quality, and supplier quality as we approach market release. You will be a hands-on leader, writing SOPs, guiding engineering teams, and partneri...Read More>>.

Let's begin! Vice President Mgr-Government, Public & Regulatory Affairs (15241)At Moody's, we unite the brightest minds to turn today’s risks into tomorrow’s opportunities. We do this by striving to create an inclusive environment...Read More>>.

Director - Regulatory Affairs Lifecycle Management Medicines Location: London, GB, SW11 7BW At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All....Read More>>.

Moody’s is seeking a Vice President for Government, Public & Regulatory Affairs to lead regulatory engagement and policy analysis across EMEA, supporting Moody’s insurance business growth. You will draft regulatory submissions, influence senio...Read More>>.

Synergy Spine Solutions is seeking a Director of Sales (International) to own and grow the business outside the United States. You will lead and scale distributor networks across EMEA, APAC, and Canada, while shaping market access, training, and r...Read More>>.

Moderna is seeking an experienced CMC Regulatory Affairs professional to lead global CMC strategies and oversight for international submissions in London. The role requires coordinating regulatory filings, ensuring health authority compliance, and...Read More>>.

At Moody's, we unite the brightest minds to turn today’s risks into tomorrow’s opportunities. We do this by striving to create an inclusive environment where everyone feels welcome to be who they are—with the freedom to exchange ideas, think...Read More>>.

Sizewell C is recruiting a Head of Regulatory Affairs to lead regulatory, licensing, compliance and integrated management systems across a major UK energy project. This senior role reports to the Safety, Security & Assurance Director and shapes re...Read More>>.

London, GB, EC2R 7BP Manchester, GB, M1 4HNHead of Regulatory AffairsSizewell C is entering an exciting phase of growth as we mature into an independent organisation and continue building one of the UK’s largest and most impor...Read More>>.

CoMind is seeking a senior software leader to manage a cross-functional DevOps and test engineering team within a regulated medical device environment. You will set priorities, develop plans, drive performance, and remain hands-on in the technical...Read More>>.

Sizewell C is entering an exciting phase of growth as we mature into an independent organisation and continue building one of the UK's largest and most important energy projects. We are now recruiting the below position: Head of Regulat...Read More>>.

Sizewell C Company is seeking a Head of Regulatory Affairs to lead regulatory, licensing and compliance across the organisation. The role reports to the Safety, Security & Assurance Director and oversees Regulatory Affairs, Licensing, Nuclear Comp...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>>.

Moody's in London seeks an AVP, EMEA Regulatory Affairs to support regulatory strategy across the EMEA region through stakeholder engagement, thought leadership, and cross‑functional collaboration.The role manages relationships with regul...Read More>>.

The RoleJoining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. Moderna is strengthening its presence in Lond...Read More>>.

CoMind is developing non-invasive neuromonitoring tech in London. This leadership role heads the product software stack, managing a team across embedded C++, GUI, and firmware, shaping architecture and delivery from prototype to production....Read More>>.

Merck & Co., Inc. is seeking a hands-on Associate Director, Regulatory Affairs – Power Platform Solutions Specialist. You will implement and maintain Power Apps UI changes, manage Dataverse security and data models, and automate workflows across...Read More>>.

Location City, Belfast Job Type Permanent PostedLocation: Belfast, United KingdomThales is a global technology leader with more than 83,000 employees on five continents. With over 7,500 people in the UK, operating across d...Read More>>.