Pharma Regulatory Affairs Specialist: Documentation Expert

22 set - Anagni
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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

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