Quality Assurance
promeatherapeutics
Job Description
- Responsible for review of stability protocol & report.
- Responsible for Preparation of Annual Product Quality Review.
- Responsible for review of Master Packing Card & Master Formula Card.
- Responsible for preparation and review of Process validation Protocols and reports.
- Responsible for review of Batch Manufacturing and Batch Packing records
- Responsible for preparation of batch release certificate and ensuring batch release process performed as per the SOP.
- Responsible for issuance of Formats, Logbooks, Register, protocol, reports, BMRs and BPRs as per respective procedure.
- Responsible for review of QC documents such as Specifications and Standard Testing Procedure (RM, bulk, finished product, RST).
- Responsible for review of COAs (Raw Material, Packing Material & Finished Product).