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

Takeda UK

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

Job Summary

  • The role leads the therapeutic area regulatory strategy team to secure timely approvals for new products and manage life cycle variations in China.
  • Candidates must possess deep expertise in local regulatory requirements including NMPA, CDE, and NIFDC to de-risk drug development.
  • The position requires managing internal and external stakeholders while fostering a culture of compliance, collaboration, and operational excellence.

Matching Summary

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

Skills & Requirements

Must-have

  • 15 years regulatory affairs experience
  • 5 years people management experience
  • In-depth China NMPA regulatory knowledge
  • Strategic product lifecycle management
  • Cross-functional team leadership

Nice-to-have

  • Experience in global environment
  • Strong stakeholder relationship building
  • Ability to anticipate emerging issues
  • Culture of high performance and adaptability

Key Requirements

  • Bachelor's degree in medicine or pharmacy
  • 15 years related work experience in regulatory affairs
  • 5 years experience in people management
  • Must be based in Beijing, China

Work Rights

Not specified

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