Regulatory Affairs CMC Associate Director
KI-Beschreibung
In this role, you will drive the global regulatory strategy for CMC, ensuring compliance and quality in submissions. Your day-to-day responsibilities will involve collaborating with cross-functional teams, negotiating with health authorities, and providing strategic guidance to enhance project outcomes.
Anforderungen
8 Jahre von Vorteil- •Science degree (Chemistry, Pharmacy, Biochemistry, Molecular Biology, Biotechnology, Biology) or equivalent
- •Minimum 8 years regulatory experience preferred or pharmaceutical industry experience
- •Substantial knowledge
/ experience in regulatory submission and approval processes