Cencora is seeking a regulatory affairs professional with strong expertise in Analytical/Cell & Gene Therapy. The role focuses on pharmacovigilance, safety surveillance, and regulatory deliverables across product lifecycles in a global context.
Collaboration with clients and internal teams is essential to ensure compliant, timely outcomes. The idóneo candidate has 4+ years in this field, plus ATMP/Gene therapy experience and US/EU CMC regulatory knowledge.