"• 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."

📌 Assistant Manager (Dholka)
🏢 Cadila Pharmaceuticals
📍 Dholka