Title:  Executive - QA

Review BMR's and analytical documents.
2.        Issuance, retrieval, distribution and destruction of all QA related documents.
3.        Issuance of Batch Manufacturing records and allocation of Batch.
4.        To ensure compliance with existing SOPs, CGMP/CGLP.
5.        Ensure that documents issued retrieval, and destruction as per procedure.
6.        Monitoring of calibration of process equipments and related documents.
7.        Monitoring of Packing related activities and related records.
8.        Sampling of finished product and related records.
9.        Check and review of cleaning related documents.
10.        Review of production related documents.
11.        Timely document support to regulatory & customer audit compliance.
12.        Ensure that sampling, dispatch and labeling activities is being carried out as per procedure.
13.        To release the finished product after reviewing Batch documents.
14.        Review and maintain the vendor updating procedure.
15.        Preparation and review of the data for annual product review.
16.        Stability Study management.
17.        Handling of Quality Risk Management