





As a summer intern in Regulatory Affairs at Roche AB, you will have a unique opportunity to experience working with regulatory matters while contributing to the team during the summer holiday period. You will work closely with our experienced Regulatory Affairs Managers and support the team in daily operations. This role provides an overview of how medicines are approved and monitored to ensure the highest levels of patient and product safety. Your main responsibilities include: Product Information: Reviewing and updating labeling materials, patient information leaflets, and Summaries of Product Characteristics (SmPC) for the Swedish market. Compliance: Ensuring our product information consistently complies with current legislation and internal guidelines. Fass.se: Administering texts on fass.se (the Swedish medicines portal). Collaboration: Working alongside colleagues in departments such as Quality Assurance, Medical and Marketing.