Principal task: 1) To maintain and observe GLP in working setting in GC. 2) Timely respond development of the Regulatory Queries of products. 3) Preparation of COAs Responsibilities: 1) Preparation of New Analytical method validation and Method Transfer Protocol and Report as per the current Regulatory requirement. 2) Prepare Protocol of analytical method validation and method transfer report and routine analysis data. 3) Preparation of standard operating procedure. 4) Maintaining GC calibration report. 5) Trouble shooting during day to day analysis with proper instrument carc. 6) Taking care of PM of all the instrument of Analytical GC.
📌 Research Associate (India)
🏢 Cadila Pharmaceuticals
📍 India
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