Description:
- 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.

📌 Senior Executive (Dholka)
🏢 Cadila Pharmaceuticals
📍 Dholka