About this opportunity
Takeda lists this Site CMC Regulatory Director — Post-Approval Strategy opportunity in boston, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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
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Worksite address
boston, MA, 02298, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.