About this role
"• 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."