Graduate - Regulatory Affairs

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. Our Regulatory Affairs teams bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medicinal products, practices and solutions to the EMEA region, including the UK.

This role will be based in our modern state-of-the-art co-working facilities in Moorgate, London. This site, at the heart of London provides fantastic amenities, support services and collaborative work spaces with convenient transport links. We are a global biopharmaceutical leader committed to enhancing the lives of individuals through a diverse portfolio of prescription medicines, oncology treatments, life-saving vaccines, and animal health products.

Our unwavering dedication to delivering innovative solutions is the driving force behind everything we do.

Hybrid

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No. Job Posting End Date: 10/13/2026.
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• 12 months in International Regulatory Affairs CMC In Regulatory CMC (Chemistry, Manufacturing and Controls) our experts maintain the scientific and technical aspects of products that ensure patients receive medicines that are manufactured and tested to a high quality and within compliance of the requirements of the world's Health Authorities. International Regulatory Affairs CMC is a key component of our company's strategy to build regional Chemistry Manufacturing and Controls regulatory knowledge and effective local relationships with country offices to deliver appropriate regulatory strategies and on-time regulatory submissions.
  
  As part of the EMEA team you will be one of the regional experts for CMC in EU, Eastern Europe, Middle East and Africa. Learn, assess, and apply regulatory policies, internal processes, and systems. Support the development of regulatory strategies and the review of submission packages for the EMEA region. Contribute to new marketing authorisation submissions and product lifecycle management activities.
  
  Collaborate with colleagues across the region and globally to deliver regulatory objectives. Participate in health authority interactions and support regulatory engagement activities. Contribute to operational excellence and regulatory science initiatives while developing digital skills through the use of innovative tools and technologies.
• 12 months in Regulatory Affairs UK The Country Regulatory Affair team in the UK manages a broad portfolio of prescription medicines for the UK, largely across the vaccine, oncology and infectious disease therapeutic areas and this role is accountable for undertaking a variety of regulatory activities across a range of products for the UK market. Support the development of regulatory strategies and regulatory submissions for new marketing authorisation applications and product launches.
  
  Contribute to the lifecycle management of marketing authorisations, ensuring ongoing regulatory compliance. Participate in MHRA interactions and support regulatory engagement activities. Support the development and maintenance of patient information leaflets, packaging components, and artwork, in line with regulatory requirements and company…