Site Quality Director – Pharma Ops (CDMO)

Our Client seeks a Pharmaceutical Activities Site Director to establish and lead a brand-new pharma logistics site in Louvres, France. The role focuses on building QA operations from scratch with high autonomy, including future batch release as onboarding progresses.

The candidate will oversee quality, regulatory affairs, and QMS implementation, ensuring GMP/GLP compliance and successful interactions with ANSM and other authorities. Fluency in French and English is required.