Cadila Pharma

"•	Follow cGMP and GLP practices in Microbiology lab- Main pharma QC laboratory.
•	To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by respective specification and SOP.
•	To follow safety Procedure in Microbiology laboratory (Main Pharma-QC)
•	To attend the training as per schedule.
•	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.
•	 Preparation and sterilization of media for analysis.
•	Used media destruction as per respective SOP.   
•	Responsible for cleaning & monitoring of laboratory.
•	Responsible for online documentation. 
•	Sampling and Microbiological/ chemical testing of Purified water, Water for injection, Potable water samples and pure steam condensate samples.
•	Plate / Tube verification and release and on-line data recording 
•	Work allocation and distribution
•	To ensure the training about the changes in standard operating procedures (SOP), if required.
•	Review of analytical data 
•	 Change control, master document preparation and review 
•	Regulatory Audits and Periodic self-inspection 
•	Do any other Work assign by HOD."

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