Proficient quality control analyst with 4 years of involvement with Analytical Method Development and Validation in Research and Development Department in the Pharmaceutical industry. Can involve rationale and thinking to distinguish shortcomings and open doors for development. Careful, exact and thorough with incredible critical thinking capacities. Thorough and coordinated with profound information and experience working in full consistence inside cGMP, FDA 21 CFR, USP-NF, British pharmacopeia, European pharmacopeia and ISO guidelines, completely equipped for utilizing LIMS, Empower and all significant research facility advancements as HPLC, UPLC, GC and Wet Chemical equipment.