#Well versed with LATEST GUIDELINES OF USFDA and MHRA on DATA INTEGRITY
#Handling Quality Assurance Activity's . Should have worked in a REGULATORY Formulations Plant
#Exposure of Regulatory audits like MHRA, USFDA, TGA, MCC, MHRA, EU & Other RA
#QMS (Quality Management System): Excellent investigation and evaluation skill in CAPA Management, Incidents/Deviations, Change Controls, OOS investigations, Product Quality Review, Batch Release, Training Management and Document control system.