Senior Staff Specialist, Regulatory Affairs
KI-Beschreibung
In this role, you will be a key technical expert, driving regulatory strategy and ensuring compliance throughout the product lifecycle. You will collaborate with various teams, negotiate with authorities, and guide submissions to facilitate global market access.
Anforderungen
6 Jahre- •Minimum 6 years of regulatory affairs experience in medical devices or highly regulated industry
- •Strong knowledge of global regulatory pathways and submission requirements
- •Experience developing regulatory strategies and interacting with regulatory authorities