Manager, China Cmc Regulatory Affairs

Takeda UK

Beijing, China
Develop global regulatory strategies
Manage regulatory submissions
Strong leadership skills
The role involves developing and executing global regulatory strategies for assigned programs. Collaboration with regional counterparts is essential to align these strategies effectively. The manager will also lead and mentor junior staff, enhancing the team's capabilities in regulatory affairs

Job Summary

  • The role involves developing and executing global regulatory strategies for assigned programs. Collaboration with regional counterparts is essential to align these strategies effectively. The manager will also lead and mentor junior staff, enhancing the team's capabilities in regulatory affairs.
  • The position requires expertise in CMC requirements and the ability to negotiate with health authorities. Excellent communication skills are necessary to convey complex information clearly. The manager will ensure compliance and timely submissions for regulatory documents.
  • This full-time role is based in Beijing, China, and offers opportunities for professional growth within a leading pharmaceutical company.

Matching Summary

The role involves developing and executing global regulatory strategies for assigned programs. Collaboration with regional counterparts is essential to align these strategies effectively. The manager will also lead and mentor junior staff, enhancing the team's capabilities in regulatory affairs.

Skills & Requirements

Must-have

  • Develop global regulatory strategies
  • Manage regulatory submissions
  • Strong leadership skills

Nice-to-have

  • Effective cross-functional collaboration
  • Proficient in mentoring junior staff
  • Skilled in risk mitigation

Key Requirements

  • Expertise in CMC requirements
  • Proven negotiation skills with health authorities
  • Experience in regulatory submissions

Work Rights

Not specified

Tailored Resume

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