Pharma Regulatory Affairs Lead – Documentation

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

Brenntag is seeking a Regulatory Affairs Specialist to oversee regulatory documentation and compliance for the pharma business across the EMEA region.

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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. xysqume

A life sciences degree and fluency in English and Italian are required.

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