 A Proven Analytical professional with 12 yrs of experience in the pharmaceutical field with work experience spanning across Analytical Research and development (AR&D) and Quality Assurance in a cGMP environment. Demonstrated ability to handle analytical projects independently and handled the Projects as a lead . Handled auditing preparation responsibilities for USFDA, WHO, MHRA audits.  Has rich experience in handling stability, method transfers, method validations, development activities, Rich experience in Qualification activities like IQ, OQ & PQ of laboratory equipment and setting of Lab. Trained and Qualified lead investigator in handling the Lab investigation, OOS, Change control and Deviation. Trained and Qualified reviewer (undergone training for review) in reviewing the documents related to calibration, Qualification and GMP stability.