Role Summary:  

The Quality Assurance Specialist is responsible for ensuring that all required information and documentation are properly reviewed, evaluated, and approved to confirm that pharmaceutical products meet the intended quality standards and regulatory requirements. The role involves coordinating and controlling quality-related activities in compliance with approved procedures, Pharmaceutical Quality Systems, and SFDA regulation

Responsibilities:   

1. Batch Record Audit & Release

• Receive, review, audit, and verify batch record documentation.
• Ensure all batch records are complete, accurate, and compliant with approved procedures and GMP requirements.
• Identify incomplete data, discrepancies, or calculation errors and coordinate correct...