Director, Regulatory Affairs CMC
KI-Beschreibung
In this role, you will lead regulatory support for CMC programs, ensuring effective strategies for global submissions. Your daily responsibilities will include collaborating with teams, managing documentation, and maintaining relationships with regulatory authorities to drive project success.
Anforderungen
10–12 Jahre- •10-12+ years of related work experience
- •8+ years in Regulatory Affairs CMC in Biotech
/ Pharmaceutical industry - •Experience in small molecule drug development