Job Description:

• 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 Dholka
🏢 DigiCAD
📍 Dholka