Senior Manager Regulatory Affairs CMC
KI-Beschreibung
In this role, you will define and implement regulatory strategies for biosimilars, ensuring compliance while managing submissions and interactions with health authorities. Your daily responsibilities will include collaborating with cross-functional teams and staying updated on regulatory changes to support project development.
Anforderungen
5–8 Jahre- •5-8 years Regulatory Affairs CMC experience in Biotech
- •Master’s Degree in Life Science or related discipline
- •Experience in managing international regulatory submissions