Clinical Program Quality, Associate Director, R&d, China

Takeda

Shanghai, China
Gcp-related quality assurance experience
Inspection readiness programs management
Risk-based audit strategy implementation
The role involves providing quality assurance oversight for clinical research programs in various business units

Job Summary

  • The role involves providing quality assurance oversight for clinical research programs in various business units.
  • The Associate Director will lead inspection readiness programs and manage inspection activities.
  • Candidates should possess extensive knowledge of ICH GCP and global regulations.

Matching Summary

The role involves providing quality assurance oversight for clinical research programs in various business units.

Skills & Requirements

Must-have

  • GCP-related Quality Assurance experience
  • Inspection readiness programs management
  • Risk-based audit strategy implementation

Nice-to-have

  • Collaborative team player
  • Strong technical writing skills
  • Ability to negotiate and influence

Key Requirements

  • BA/BS degree required
  • Minimum of 10 years experience
  • Fluent in Mandarin

Work Rights

Not specified

Tailored Resume

Cover Letter