Maintain GLP in the laboratory as per regulatory requirement. Analytical method development as per ICH Guidelines. To perform In-process, routine and stability sample analysis. Perform the analytical method verification / validation as per protocol. Analytical method transfer to QC Laboratory. Documentation as per the GLP requirement. Trouble shooting during day to day analysis with proper instrument care. Perform dissolution development, multimedia dissolution and CDP activity. Working standard preparation as per SOP.
📌 Research Associate Dholka
🏢 Cadila Pharmaceuticals
📍 Dholka
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