Pharma Regulatory Affairs Specialist – Documentation

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7eevk8

Brenntag is seeking a Regulatory Affairs Specialist to manage regulatory, quality, and compliance activities for the pharma portfolio across the region. This role focuses on providing accurate, audit-ready documentation to pharmaceutical customers and supporting regulatory deliverables for bespoke projects.
Based in a pharma-focused team, you will collaborate with commercial, supply chain, QHSE, and supplier partners to ensure materials meet regulatory standards and industry guidelines, with
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Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7eevk8