Regulatory Affairs Manager - Biopharma (Boca Raton)

ADMA Biologics seeks a skilled Manager, Regulatory Affairs to lead regulatory submissions and strategy for Boca Raton operations. The role involves coordinating INDs, BLAs, CTD documents, and lifecycle submissions, while guiding cross-functional teams and liaising with FDA and other regulators.

The position requires extensive regulatory experience across drug development, strong communication abilities, and a thorough understanding of GMP, GCP, and documentation practices.