Takeda in Boston, MA is seeking a Director Regulatory Site CMC to lead site-specific post-approval change management and regulatory submissions across small molecule and biologics. This role requires 10+ years in biopharma with deep global HA regulatory experience, an advanced scientific degree, and proven ability to communicate regulatory strategy to cross-functional teams.
The position offers a hybrid work arrangement, competitive compensation, and opportunities to drive standardization and
#J-18808-LjbffrSite CMC Regulatory Director: Global Change & Submissions in cambridge at Unknown Company
This position is listed as full time and hybrid.