Global Regulatory Affairs CMC Director — Lead Submissions

A global pharmaceutical company in Boston seeks an experienced Regulatory CMC Product Lead with over 10 years in the biopharmaceutical industry, including substantial experience in regulatory affairs for drugs and devices. The role demands a strategic mindset to navigate regulatory complexities and lead submissions. Ideal candidates should have advanced scientific degrees, exceptional leadership capabilities, and skills in analytical thinking and communication. This position offers a hybrid work model and a competitive salary range from $174,500 to $274,230. #J-18808-Ljbffr