Timely validation of all instruments in laboratory. All documents required for Regulatory compliance are maintained properly. To report any OOS/incidents/deviation discrepancy in laboratory analyst to section in charge/QC In-charge. To ensure analytical documents like specification, protocol, STP are prepared as per SOP. To maintain instruments logbooks as per analysis. To educate and train workmen and implement in protected handling of media, reagents, cultures, chemicals, gas cylinder, laboratory instruments to prevent accidents. Review of microbial analysis data for sustainability and API analysis data whenever required.
📌 Executive (India)
🏢 Cadila Pharmaceuticals
📍 India
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