Manager, Quality Assurance, Investigational Medicinal Products Pipeline Development, Shonan Ipark / 湘南アイパーク 治験薬品質保証‐開発担当 課長代理

Takeda

Fujisawa, Japan
Business level japanese
Gmp compliance monitoring
Quality assurance in drug development
Takeda aims to contribute to the health and brighter future of people worldwide

Job Summary

  • Takeda aims to contribute to the health and brighter future of people worldwide.
  • The department ensures compliance with GMP requirements in clinical trial drug development.
  • Employees are encouraged to thrive in a diverse and inclusive environment.

Matching Summary

Takeda aims to contribute to the health and brighter future of people worldwide.

Skills & Requirements

Must-have

  • Business level Japanese
  • GMP compliance monitoring
  • Quality assurance in drug development

Nice-to-have

  • Ability to negotiate with stakeholders
  • Mentoring and support skills
  • Proactive problem-solving abilities

Key Requirements

  • Bachelor's degree in relevant science
  • 8+ years of experience in quality assurance
  • Knowledge of GMP requirements

Work Rights

Not specified

Tailored Resume

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