Executive Job in Cadila Pharmaceuticals Ltd at Dholka

"• 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."