- Analysis (Routine ,Stability and QBD analysis) of ongoing projects by performing analysis of various tests (e.g. Dissolution, assay, Related substances test, or as per requirement) within given Time
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- Analytical Method development as per current SOP/guideline wherever required.
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- Regulatory query/Plant Query related analysis for different products.
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- To follow Good Laboratories practice while working.
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- Documentation and compliance of data generated on all analytical activities as per the GLP/GMP norms and to keep working place neat and clean.
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- Effective utilization of all available resources like instruments, apparatus etc.
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- Method transfer at plant.
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- Method equivalency, method verification, pharmaceutical equivalency analysis of Pharmacopeial method.
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- Preparation of various documents like method transfer waiver, method equivalency report, cleaning validation report, SOP’s, T-STP/FP STP etc.
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- Maintenance of documentation as per the SOP according to the GLP practices.
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- To undergone training as per requirements to upgrade knowledge and current requirements.
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