Supervise members responsible for checking production records, determining shipments, and handling complaints, ensuring reliable execution and continuous improvement of each process
Job Summary
Supervise members responsible for checking production records, determining shipments, and handling complaints, ensuring reliable execution and continuous improvement of each process.
Ensure the quality of manufacturing records while achieving timely shipment decisions and oversee complaint handling, ensuring prompt escalation to the Senior Leadership Team when necessary.
Comply with laws and regulations related to ensuring the quality, efficacy, and safety of pharmaceuticals, medical devices, GMP Ministerial Ordinances, GCTP Ministerial Ordinances, and corporate policies.
Matching Summary
Supervise members responsible for checking production records, determining shipments, and handling complaints, ensuring reliable execution and continuous improvement of each process.
Skills & Requirements
Must-have
Quality management systems knowledge
Manufacturing record inspection
Shipment judgment process
Complaint handling process
Regulatory compliance
GxP regulated industries experience
Nice-to-have
Collaboration and teamwork
Customer focus
Continuous improvement promotion
Business conversation level English/Japanese
Key Requirements
Degree in pharmacy, science, or engineering preferred