Takeda in Boston, MA is seeking an experienced GRA CMC Product Lead to develop and oversee regulatory CMC strategies for assigned products, guiding submissions from development through lifecycle.
You will represent Regulatory, Pharmaceutical Development, and Commercial teams in Health Authority meetings, mentor GRA CMC members, and drive regulatory compliance across global programs in a hybrid work model.
#J-18808-LjbffrGlobal Regulatory CMC Director - Submissions Lead (Hybrid) in cambridge at Unknown Company
This position is listed as full time and hybrid.