A University Gold Medalist with +14 years of regulatory experience in developing, leading and implementing global regulatory CMC strategies to secure and maintain market access for assigned products in line with business objectives and in coordination with key internal stake holders.+8 years experience as a Quality Investigator (Escalations, Market Complaints, Deviations, Quality Events, CAPAs, Root Cause Analysis and define Effectiveness checks)+8 years experience in preparing site for audits, participation in regulatory audits and qualifying external sites (CROs).+8 years experience for developing strategy and managing activities involving GMP Quality Assurance and Compliance with relevant regulatory and quality guidelines.+2 years regulatory experience in clinical development life cycle.Developed Digital tool to monitor DEPRESSION in cancer patients.Research in Cancer therapies using "Photo dynamics", "Protein Kinase inhibitors", "Peptides" and "siRNA delivery systems". Well versed with data sciences and software used in research. Volunteering and supporting Cancer research.