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 integral context.Collaboration with clients and internal teams is essential to ensure compliant, timely outcomes. The ideal candidate has 4+ years in this field, plus ATMP/Gene therapy experience and US/EU CMC regulatory knowledge.#J-18808-Ljbffr
📌 Eu Regulatory Affairs Lead: Ctr/Ctis Strategy & Submissions (Madrid)
🏢 Cencora
📍 Madrid
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