• 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.
📌 Technical Supervisor (India)
🏢 Cadila Pharmaceuticals
📍 India
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