Experienced Scientist with a demonstrated history of working in the pharmaceuticals industry. Skilled in Research and Development (R&D).Proficient, investigative method development & analytical scientist with 6.5 years’ experience applying deep technical aptitude and exceptional scientific acumen to drive innovation, design and development of analytical methods. Skilled at managing AR&D projects simultaneously with personnel and resource management, and working efficiently with cross functional teams & multicultural environments. And 2.5 years experience in DQA with handling of Incidents, CAPA, OOS, OOT, Internal audits, Computer system validation and review of Specifications, STP’s, SOP’s, Analytical method validation, method transfer protocols and reports. - Expertise in analytical method development, method validation, method transfer, routine and stability analysis for oral and semisolids dosage forms.- Knowledge of regulatory guidelines and practices including ICH, US FDA, cGMP/cGLP, and QbD/DoE.