1. To perform the activities for Laboratory Quality Assurance in shifts to support Review, Release and Non-Conformance Investigation Quality Control. Issuance/Review and should ensure the facility in cGMP/GLP compliance. 2. Monitoring laboratory activities compliance with company policy and cGMP/cGLP regulations. 3. Issuance of logs format to user departments. 4. Review of raw data and release of test reports of raw materials ,Finished product and stability.