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>>.

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>>.

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>>.

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 support regulatory activities across the business, collaborating with engineers and scientists to align development with global requirements. You will help operate the quality management system and guide teams thr...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 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 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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

Cure Talent are delighted to be partnered with a global medical device company recognised for its life-saving technologies. As they continue to expand their portfolio, we have an opportunity for a Senior Regulatory Affairs Specialist to join th...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>>.

Inspiration Healthcare seeks a Head of Quality Assurance and Regulatory Affairs in the UK to lead the Quality Assurance and Regulatory Affairs function, ensuring MDR compliance and regulatory registration across key markets. The role drives a cult...Read More>>.

Job Purpose (Role Definition)The Head of Quality Assurance and Regulatory Affairs:will manage the Quality Assurance and Regulatory Affairs function.is appointed as the person responsible for regulatory compliance,...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>>.

Balance technical, regulatory and commercial challenges in this fulfilling role. This highly regraded Cambridge-based medical technologies company is seeking a proven engineering leader to help guide high-value development programmes from conce...Read More>>.

Responsible for developing and managing the company's compliance framework for e-cigarette and medical device products across the UK and European market. This role monitors evolving UK and European regulatory requirements, leads product certifi...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>>.

Contract Type: Unlimited / Full-Time Country / City: United Kingdom / Birmingham Company: Beiersdorf UK Ltd. Job Function: Quality Management Your Tasks Strategy & Compli...Read More>>.

Beiersdorf UK Ltd. is seeking a senior Quality Management & Regulatory Affairs leader to drive strategy and ensure compliance across Northern Europe. You will lead the QMS, oversee supplier quality and product releases, and manage regulatory regis...Read More>>.

Phillips Medisize, a Molex company, is seeking an engineer to lead design and proof activities for smart inhalation and nebuliser systems. You will translate design inputs into specifications, develop prototypes, and drive verification and validat...Read More>>.

The HCIB Regulatory Affairs Senior Manager will be part of a small team which has broad remit and responsibilities, including and not limited to: identification and oversight of upcoming and in-train material regulatory compliance developments, su...Read More>>.

About ECI ECI’s mission is to be the global leader of professional consulting services for the life sciences industry. Our clients lean on our diverse perspectives and decades of expertise to tackle their toughest challenges and we take...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>>.

Job Description 24-Month Regulatory Affairs Graduate Programme featuring rotations in International Regulatory Affairs CMC and UK Regulatory Affairs, with exposure to regulatory strategy, submissions, compliance, and health authority engagement. O...Read More>>.

MSD is offering a 12-month Regulatory Affairs CMC student placement in Moorgate, London, delivering hands‑on exposure to regulatory strategy, submissions management, health authority engagement, and operational excellence projects across the EME...Read More>>.

Job Description 12-Month Regulatory Affairs CMC Student Placement offering exposure to regulatory strategy, submissions management, health authority engagement, and operational excellence projects. Our Regulatory Affairs team...Read More>>.

Job Description24-Month Regulatory Affairs Graduate Programme featuring rotations in International Regulatory Affairs CMC and UK Regulatory Affairs, with exposure to regulatory strategy, submissions, compliance, and health authority engag...Read More>>.

MSD in London offers a 24-month Regulatory Affairs Graduate Programme with rotations in International Regulatory Affairs CMC and UK Regulatory Affairs, exposing you to strategy, submissions, compliance and health authority engagement.Based...Read More>>.

MSD Malaysia in London invites applications for a 24-month Regulatory Affairs Graduate Programme, with rotations across International Regulatory Affairs CMC and UK Regulatory Affairs, exposure to strategy, submissions, compliance and health author...Read More>>.

Job Description 12-Month Regulatory Affairs CMC Student Placement offering exposure to regulatory strategy, submissions management, health authority engagement, and operational excellence projects. Our Regulatory Affairs team bring new medical adv...Read More>>.

JOB DESCRIPTION: Medical Device Inventory Coordinator Location: Witney Bring your passion, ideas and purpose to life in a company that can truly help you achieve your full potential Abbott has bee...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 Assess...Read More>>.

Sanofi is offering a Head Office placement in Regulatory Affairs for a Life Science undergraduate returning to university after completion. The role provides hands-on regulatory work across UK & Ireland, with opportunities to contribute to product...Read More>>.

NBCUniversal is one of the world's leading media and entertainment companies. We create world-class content, which we distribute across our portfolio of film, television, and streaming, and bring to life through our global theme park destinations,...Read More>>.