Director, Therapeutic Area Head Of China Regulatory Strategy, Gastrointestinal And Inflammation

Takeda

Beijing, China
15 years regulatory affairs experience
5 years people management experience
In-depth knowledge of china nmpa regulations
The role leads the therapeutic area regulatory strategy team to secure timely approvals for new products and manage life cycle variations

Job Summary

  • The role leads the therapeutic area regulatory strategy team to secure timely approvals for new products and manage life cycle variations.
  • Candidates must possess deep knowledge of local Chinese regulatory requirements including NMPA, CDE, and NIFDC interactions.
  • The position requires fostering a culture of high performance while partnering with global and regional functions to advance the pipeline.

Matching Summary

The role leads the therapeutic area regulatory strategy team to secure timely approvals for new products and manage life cycle variations.

Skills & Requirements

Must-have

  • 15 years regulatory affairs experience
  • 5 years people management experience
  • In-depth knowledge of China NMPA regulations
  • Strategic planning for drug development
  • Cross-functional team leadership

Nice-to-have

  • Experience in global environment
  • Strong stakeholder relationship building
  • Ability to anticipate emerging issues
  • Cultural competence in diverse teams

Key Requirements

  • Bachelor's degree in medicine or pharmacy
  • 15 years related work experience
  • 5 years people management experience

Work Rights

Not specified

Tailored Resume

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