Takeda drives innovation to enrich patients' lives and provides growth opportunities for its employees
Job Summary
Takeda drives innovation to enrich patients' lives and provides growth opportunities for its employees.
This position is responsible for executing validation activities at the Narita plant, ensuring equipment, systems, and processes are qualified and in continuous cGMP compliance.
The role involves managing validation personnel and projects within quality, time, and budget constraints, requiring excellent organizational and project management skills.
Matching Summary
Takeda drives innovation to enrich patients' lives and provides growth opportunities for its employees.
Skills & Requirements
Must-have
Native level Japanese proficiency
cGMP compliance
Validation strategy development
Cross-functional team coordination
Regulatory authority inspection support
Nice-to-have
Proactive problem-solving
Adaptability to changing environments
Commitment to patient well-being
Key Requirements
Bachelor's degree in Engineering or Science
Experience with manufacturing processes and control systems
Experience interacting with FDA and other regulatory authorities