Job Description
Regulatory Affairs Intern
We are seeking a motivated Graduate Intern to join our Regulatory Affairs Programme within a Global Regulatory Sciences team supporting the UK and Ireland region. This role offers hands-on experience in regulatory strategy, planning and operational execution across a diverse product portfolio. The successful candidate will gain exposure to clinical trial and medicinal product licensing legislation and learn how regulatory requirements are applied throughout the product lifecycle, from development through commercialisation. You will support regulatory assessments, help maintain marketing authorisations and collaborate closely with cross-functional teams to ensure compliance while contributing to successful product delivery. This opportunity is ideal for a recent life sciences graduate looking to build a strong foundation in pharmaceutical regulatory affairs within a collaborative and fast-paced environment.
Our organisation is a global, research-driven biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that address serious diseases. With a strong commitment to scientific excellence, collaboration and patient-focused innovation, the company works across international markets to advance healthcare through cutting-edge research and development. Employees benefit from a supportive, inclusive culture that encourages learning, professional growth and meaningful contributions to improving patient outcomes worldwide.
Key Responsibilities
* Support regulatory planning, strategy and operational activities across assigned product portfolios.
* Assist with preparation and maintenance of regulatory submissions and marketing authorisations.
* Monitor and interpret UK and EU pharmaceutical regulatory requirements and legislative updates.
* Contribute to regulatory assessments supporting clinical trials and product lifecycle management.
* Collaborate with cross-functional teams including Research & Development and commercial teams.
* Maintain accurate regulatory documentation and tracking systems.
* Support compliance activities to ensure products meet applicable regulatory standards.
* Participate in team meetings, projects and learning opportunities within the Regulatory Affairs function.
Requirements
* Recently graduated with a degree in medicine, pharmacy, life sciences or a related scientific discipline.
* Strong analytical and problem-solving skills.
* Ability to work both independently and collaboratively within a team environment.
* Self-motivated, proactive and highly organised with strong attention to detail.
* Excellent written and verbal communication skills.
* Good computer literacy, including familiarity with standard office software.
* Interest in pharmaceutical regulation, clinical development and healthcare innovation.