Cadila Pharma

•	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 follow safety procedure in qc department.
•	To analyze the Sample of  in process validation and finish product on instrument such HPLC, GC, UV, FTIR 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 online documentation. 
•	To do any other Work assign by HOD.

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