via Career pages·Yesterday

Technical Supervisor

Cadila Pharmaceuticals

Full-timeOn-sitemicrobiology laboratory operationscgmp complianceglp compliancesample analysisstability testinginstrument sterilizationmedia preparationsop trainingregulatory auditschange controldocument managementwater quality testingsafety proceduresonline documentationpurified water analysisplate and tube verificationdata recordingwork allocationtraining delivery

Location:Dholka, IndiaType:Full-timePosted:Yesterday

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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.