About this role
"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."