EMEA Regulatory Affairs Specialist – Pharma Documentation

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7d4bil

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.

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7d4bil