Regulatory Affairs & Pharmacovigilance Manager

The Regulatory Affairs & Pharmacovigilance Manager oversees regulatory and pharmacovigilance operations for the Central Cluster, ensuring compliance with local and international requirements while supporting continuous improvement initiatives. This role involves managing RA/PV activities, shaping regulatory strategies for product lifecycle management, and serving as the primary liaison with health authorities and cross-functional teams. The position reports directly to the Head of Regulatory Affairs & Pharmacovigilance, EPM, and contributes to regional and global safety strategies.