:

• 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