To perform In process, Intermediate, Process validation, Raw material, Packing material, Stability, Working standard and finished product chemical sample analysis with proper documentation. Registration off All stages sample in LIMS etc. Maintain of Inward register, instrument usage log books. Preparation and documentation of volumetric solution/regents. To ensure laboratory and instruments are clean. Ensure that GLP and safety during activity. Other activities instructed by Head QC/Designee from time to time. To ensure laboratory and instruments cleaning before start the analysis.

Maintain traceability of Working/Reference/Pharmacopeia/Impurity Standards and laboratory reagents/Chemicals.