









A GSK internship offers you the opportunity to kickstart your career – to take on a real role with genuine impact! You’ll take on challenging, serious work on live projects or assignments. You’ll also get to learn from us, develop your skills and gain valuable experience for wherever the future takes you. What will you do? You will get tailored on-the-job training from Regulatory Affairs experts and take part in meaningful tasks that support vaccine development and lifecycle management, for example: Preparation and authoring of technical regulatory documents for vaccines in compliance with the applicable regulatory & scientific standards. Help compile market specific requirements. Support the preparation of responses to regulatory authority questions. Assist with deployment and adoption of new IT tools (Artificial Intelligence & Digital fluency) for GSK vaccines within Global Regulatory Affairs. Contribute to a variety of other regulatory and cross-functional projects