Having adequate knowledge of Sampling, Testing of Raw material, Packing Material, Finish Product, Validation and Stability samples.
Sound knowledge of current industrial regulations and analytical method validation/verification activities.
Having adequate knowledge of Laboratory Instruments and equipment's Calibration, Maintenance/External calibration.
Having adequate knowledge of Preparation of laboratory chemicals, Reagents, test solution, and Volumetric solution.
Having adequate knowledge of Reference, Chemical and Working standard management i.e., Working Standard qualification and support in working standard management.
Having adequate knowledge of Data entry in SAP.
Having adequate knowledge of operation and trouble shoot of HPLC/UV/IR and other QC analytical instruments and its software. Having adequate knowledge of data entry management in inventory/Information management software of QC like LIMS software.
Having adequate knowledge of preparation of the QC documents like SOPs, Protocols and general documentation.
Having adequate knowledge of Pharma Industry Guidelines and Pharmacopoeias.
Having exposure of regulatory audit and GDP/DI compliance.
Having adequate knowledge of GLP / GMP requirements.
