Director, Global Regulatory Affairs CMC

Takeda
📍 Boston, Massachusetts, United States 💼 Full time 🕒 Posted July 04, 2026

Job Description

Description

About the role:


At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.

This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices organization, and will contribute to the team’s delivery of critical functions as follows: 

  • Independently develops the regulatory CMC strategy and leads the execution of regulatory CMC investigational, registration and post-approval strategies for their assigned product(s) and may serve as the GRA CMC Product Lead, as required. Prior experience in leading or playing a major role in preparing the CMC aspects of global registrational submissions of complex d...

  • Ready to Apply?

    Submit your application today and join our talented team at Takeda.

    Submit Application

    Job Details

    • Location Boston, Massachusetts
    • Job Type Full time
    • Category Other Management Occupations
    • Posted Date July 04, 2026
    • Application Deadline August 13, 2026