Brenntag is seeking a Regulatory Affairs Specialist to join the Pharma team in the EMEA region. The role focuses on managing regulatory aspects of pharma materials, delivering accurate, audit-ready documentation, and supporting regulatory deliverables for bespoke projects.
You will collaborate with QHSE, supply chain, and commercial teams to ensure compliance with EU regulations and industry standards; occasional travel for supplier meetings, audits, or internal workshops is required.
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📌 EMEA Regulatory Affairs Specialist – Pharma Documentation (Italia)
🏢 Airbus
📍 Italia