Regulatory Affairs Expert
KI-Beschreibung
In this role, you will navigate the complexities of drug safety and regulatory affairs, ensuring compliance with local regulations while supporting market access and pharmacovigilance efforts. Your day-to-day responsibilities will include managing product registrations, addressing complaints, and leading audits, all while maintaining a focus on quality and safety.
Anforderungen
5 Jahre- •Degree in Medicine, Pharmacy, Biology, Chemistry, or related Engineering degree
- •5 years professional experience in regulatory management or similar activity
- •Knowledge of regulatory and PV guidelines (EU, local)