Position Overview

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, implement and adhere to corporate procedures, and support local regulatory strategy at the ROPU level.

Tasks & Responsibilities

• Manage and oversee all local regulatory activities to ensure timely approvals and compliance with Swiss Health Authority requirements.
• Maintain close collaboration with Swiss Health Authorities, as well as regional and corporate DRA teams.
• Represent the organization in local, regional, and global regulatory m...