Niranjan Padia, a proactive Quality and Compliance professional with extensive experience in GMP, GCP, GLP, and GxP management. Demonstrated expertise in CMO and vendor qualification, risk-based auditing, recalls lifecycle management, and QMS implementation. Strong background in process development, technology transfer, process validation, and FDA mock audit readiness. Known for effectively leading teams, implementing quality frameworks, and providing training on FDA guidelines and compliance regulations. Holds a Master's degree in Pharmaceutical Regulatory Affairs and Validation.
March, 2022 - present
March, 2018