Brenntag is seeking a Regulatory Affairs Specialist with a technical background in pharmaceutical or related industries. 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.
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