· To perform QA related supporting functions in QC.

· Ensure GLP compliance in QC Lab.

· Review of Analytical Method Transfer/Analytical Method Validation Protocols and Reports.

· Review of Analytical documents related to Batch/Material Testing, Process Validation, Process

Verification, Hold time study and Cleaning Validation.

· Review of Out of Specification/ Out of Trend.

· Review of Stability Reports.

· Review of QC Existing Instrument Calibration & Preventive Maintenance Reports.

· Review of QC New Instruments Qualification documents.

· Daily monitoring of GLP compliance in QC Lab.

· Coordinate with QA Manager for release of Globalpharma products.

· To assist QA Manager in other activities.