Site Quality Leader: Regulatory Affairs & QP/PR

Talented France seeks a Site Head of Quality & Regulatory Affairs who will also hold Pharmacien Responsable (PR) / Qualified Person (QP) duties. The role combines full site quality ownership with regulatory affairs accountability and PR mandate in a leading biologics CRO/CDMO environment.

We require a European pharmacy diploma, 5+ years in QA/RA with at least 3 years in site leadership, and fluent English and French. Strong EU GMP/ANSM expertise and prior QP/MOT experience are preferred.