• Follow cGMP and GLP practices in Quality Control Lab. • To analyze the Sample of In process validation and finish product on non-chromatographic instrument such as FTIR, UV, Dissolution, DT , Hardness etc by following test procedure. • To attend the training as per schedule. • To follow safety procedure in qc department. • To receive the samples for analysis and making entry in Inward register. • To maintain the Instruments log books related to sample analysis. • To analyze the sample and compilation of documents. • Responsible for taking of Continuations sheet (CS) and print out Record of analysis (ROA) through LIMS. • Responsible for cleaning & monitoring of laboratory. • Responsible for online documentation. • To do any other Work assign by HOD.
• 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.
📌 Deputy Manager (India)
🏢 Cadila Pharmaceuticals
📍 India
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