Pharma Regulatory Affairs Lead – Documentation

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

Brenntag is seeking a Regulatory Affairs Specialist to oversee regulatory documentation and compliance for the pharma business across the EMEA region. The role requires collaboration with commercial, supply chain, QHSE and supplier partners to ensure all materials meet pharmaceutical regulations and standards.
The position is primarily office-based in Italy with occasional travel for supplier meetings, audits, or workshops. A life sciences degree and fluency in English and Italian are required.
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Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7dmyux