Graduate - Regulatory Affairs

Job Description

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 workspaces 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. 

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.

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 procedures.
• Develop and apply knowledge of UK and European regulatory legislation, guidelines, and processes.
• Contribute to departmental projects, meetings, and cross-functional initiatives across the Regulatory Affairs team.

• Currently studying towards, or have obtained within the last two years, a BSc degree (or equivalent qualification) in a scientific discipline, such as Chemistry, Biological Sciences, Engineering, Pharmacy, Microbiology, Virology, Molecular Biology, Biochemistry, or a related field.
• Strong communication and teamwork skills, with the ability to work effectively both independently and collaboratively.
• Demonstrates integrity, accountability, and a commitment to diversity, inclusion, and organisational values.
• Shows initiative, proactivity, and academic and digital curiosity, with a desire to learn and develop through feedback.
• Strong organisational skills and attention to detail.

Please complete the online application form by answering questions within the application and upload your CV and Cover Letter in a combined document in the ‘resume/CV’ section.

Our standard Future Talent recruitment process is: An online application, a virtual conversation and then a final assessment.

In the event of your successful progression to the next stage, one of our future talent team will contact you within two - three weeks of the application closing date. 

September 2027

 We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

Current Employees apply HERE

Current Contingent Workers apply HERE