Having Injectable Experience of Analytical Method Validation for Assay, Related Substances Content by HPLC and Residual Solvents by CC, Preparation and Review of Method Validation and Method Equivalency and Method Transfer Protocols and Reports.
To perform Gap analysis of defined procedures in Batch Manufacturing Record / Batch Packing Record / Standard Operating Procedure / Protocol and initiation of corrective actions.
First-class B.Tech / B.Pharma / B.Sc / M.Sc / M.Tech. / M.Pharm. / M.V.Sc./ or equivalent in relevant discipline with high academic attainment, with first class in graduate examination and post-graduate examination.