I formerly worked at Aurigene Pharmaceutical Services Limited. We specialize in synthesizing novel compounds, leveraging techniques like LCMS, HNMR, and HPLC to drive innovation in medicinal chemistry.With certifications in Lean Six Sigma Green Belt and PME, I contributed to enhancing compliance and operational efficiency. My role in the IPM team embodied a commitment to quality and efficiency, ensuring that research meets the rigorous standards of the Contract Research Organization (CRO) industry.I have a proven track record of enhancing compliance and operational efficiency. My experience spans regulatory compliance, scientific documentation, and submission processes, where I have developed in-depth knowledge of eCTD, non-eCTD submissions, and regulatory standards such as ICH, ISO, and AYUSH. In my role, I worked closely with cross-functional teams, ensuring stakeholder management, effective communication, and alignment with business objectives. I also managed client-driven projects, driving them to successful outcomes while adhering to regulatory guidelines and ensuring the highest quality standards. Passionate about advancing the pharmaceutical and life sciences industries, I am committed to driving excellence in every aspect of my work.