Head of Regulatory Affairs, R&D, Shanghai/Beijing
TakedaShanghai, China • Beijing, China
Posted November 17, 2025
Full Time
About the Company
We strive to transform lives. While the science we advance is constantly evolving, our core purpose is enduring. For more than two centuries, our values have guided us to do what’s right for patients and for society. We know that changing lives requires us to do things differently. We start by listening to and addressing what really matters to patients, the people who love them, and those in the healthcare system who provide care. And that’s what inspires us all to be bold, push boundaries and set new standards that open up greater opportunities. Read our community guidelines: https://takeda.info/communityguidelines
Job Description
The Vice President, Head of Greater China Regulatory Affairs is responsible for providing strategic regulatory inputs into drug development and oversight of registration, life-cycle management and maintenance of Takeda's pipeline and marketed products.
Requirements
- 12+ years of regulatory affairs experience in the pharmaceutical industry
- Master's degree and above preferred
- 10+ years in people/team management capacity
Benefits
- Opportunities for professional growth and development
