Deepika Malireddy, CQA, is an accomplished quality assurance professional with extensive experience in GxP compliance and regulatory inspections across multiple organizations. Currently serving as Director of QA Compliance at BridgeBio, Deepika oversees the vendor quality program and develops audit schedules. Previous roles include Senior Manager of GxP Inspection Management at BeiGene, where responsibilities encompassed building inspection management processes and performing risk assessments for regulatory inspections, and Senior Specialist in GxP Operations at BioMarin Pharmaceutical Inc., focusing on managing global GxP regulatory inspections. Deepika's career began at Aurobindo Pharma as a Quality Assurance Analyst and has included positions at Genentech and Dr. Reddy's Laboratories, emphasizing change control and process validation. Deepika holds a Professional Certificate in Clinical Trial Design and Management from San Francisco State University, a Master of Science in Pharmaceutics from Sri Venkateswara College of Pharmacy, and a Bachelor of Pharmacy from G. Pulla Reddy College of Pharmacy.
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