This role involves supervising members responsible for checking production records, determining shipments, and handling complaints to ensure reliable execution of each process
Job Summary
This role involves supervising members responsible for checking production records, determining shipments, and handling complaints to ensure reliable execution of each process.
The position requires strict adherence to laws and regulations related to pharmaceutical quality, efficacy, safety, GMP, and corporate policies.
Candidates must possess sufficient knowledge of quality management systems including record checking, shipment judgment, and complaint handling within a GxP regulated environment.
Matching Summary
This role involves supervising members responsible for checking production records, determining shipments, and handling complaints to ensure reliable execution of each process.
Skills & Requirements
Must-have
GxP regulated industry experience
Quality management systems knowledge
Manufacturing record inspection supervision
Shipment judgment process oversight
Complaint handling process management
Critical thinking and causal analysis
Nice-to-have
Business conversation level English
Process improvement proposal skills
Cross-functional collaboration abilities
Customer focus mindset
EHS rules compliance emphasis
Key Requirements
Experience in GxP regulated industries
Degree in pharmacy, science, or engineering preferred
Business conversation level English/Japanese proficiency