Cadila Pharma

•	Ensuring GLP compliance & Analysis of FP/In process/Validation/Raw Material samples in Penicillin QC lab, Dholka.
•	Ensuring GLP compliance & Analysis of FP/In process/Validation/Raw Material sample, Stability and Raw Material sampling in Penicillin QC lab, Dholka.
•	To ensure the compliance of GLP in Quality Control Lab.
•	To analyze the finished products, In-process and Raw Material sample by chemically / instrumental method. 
•	To receive the samples for analysis and making entry in Inward register.
•	To maintain the Instruments log books related to FP analysis.
•	To analyze the validation sample and compilation of documents.
•	To enter the finished product results through LIMS.
•	Follow cGMP in Laboratory. Responsible for online documentation. 
•	Responsible for taking of Continuations sheet (CS) and print out Record of analysis (ROA) through LIMS.

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