Site CMC Regulatory Director — Post-Approval Strategy
Listed on 2026-10-07
-
Healthcare
-
Pharmaceutical
Takeda in Boston, MA seeks a Director of Regulatory Site CMC to lead post‑approval change management across multiple sites, guiding submissions and aligning with global regulatory expectations. You will apply ICH Q12 principles, drive standardized processes, and explore automation to improve predictability and efficiency in regulatory activities.
You will communicate regulatory strategy to drug development, registration, and post‑market teams, leveraging strong leadership and collaboration
The following role is for a Site CMC Regulatory Director — Post-Approval Strategy with Takeda.
This position is for the Site CMC Regulatory Director — Post-Approval Strategy role at Takeda.
We are seeking a motivated Site CMC Regulatory Director — Post-Approval Strategy to join Takeda in Boston, MA, United States.
Consider building your career as a Site CMC Regulatory Director — Post-Approval Strategy at Takeda.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).