Site CMC Regulatory Director — Post-Approval Strategy

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