Brenntag is seeking a Regulatory Affairs Specialist with a technical background in pharmaceutical or related industries.
Si assicuri di inviare la sua candidatura con tutte le informazioni richieste, come indicato nella panoramica del lavoro riportata di seguito.
The role involves managing all regulatory aspects of the pharma business across the EMEA region, producing audit-ready documentation, and supporting regulatory deliverables for bespoke projects. xysqume
Office-based with occasional travel.
The successful candidate will collaborate with QHSE, supplier partners, and commercial teams to ensure regulatory compliance and adherence to
📌 Pharma Regulatory Affairs Specialist: Documentation Expert (Anagni)
🏢 Airbus
📍 Anagni