Director, Global Regulatory Affairs CMC
TakedaBoston, Massachusetts, United States
Posted February 6, 2026
174500 - 274230 USD
Full Time
About the Company
Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Job Description
The Director, Global Regulatory Affairs CMC will lead the execution of regulatory CMC strategies for assigned products and develop constructive relationships with internal and external colleagues. They will also provide guidance to teams on administrative procedural topics and foster a constructive working relationship with internal and/or external colleagues.
Requirements
- BS/BA Degree in a Scientific Discipline
- Advanced Degree (M.S., Ph.D., etc.)
- 10+ years of overall biopharmaceutical/device industry experience
- 8+ years of pharmaceutical Regulatory CMC and/or devices experience
- Experience in leading major submissions during LCM, development – including preparation of NDA/BLA/MAA
Benefits
- Medical, dental, vision insurance
- 401(k) plan and company match
- Short-term and long-term disability coverage
- Basic life insurance
- Tuition reimbursement program
- Paid volunteer time off
- Company holidays
- Well-being benefits
