"•Follow cGMP and GLP practices in quality control lab. •To prepare Specification Master as per STP in SAP/LIMS. •To follow safety Procedure in QC department. •Preparation of COA as per current specification for Packing samples (whenever required) •To receive the sample for analysis and making entry in inward register/LIMS. •To maintain the report within QC Department. •To provide the report to QA department for releasing the product. •To enter the results in SAP/LIMS for maintain the specification Packing Material wherever required. •To do any other Work assign by HOD."