In this role, you will represent the Regulatory Affairs Manager function within the Operative Units (OPUs) of Boehringer Ingelheim, covering a 12-month maternity leave. You will be responsible for executing all Drug Regulatory Affairs (DRA) activities in Switzerland, ensuring timely and successful product registrations in alignment with regional and local strategies. Furthermore, you will maintain the regulatory compliance and positioning of all registered and marketed products. You will implement and adhere to corporate procedures, as well as regional working instructions, processes, and systems relevant to these activities. In addition, you will contribute to local regulatory strategy and support compliance monitoring at the ROPU level.