Amanda Blount is a seasoned professional in quality assurance and regulatory compliance, currently serving as a Sr. QA Supervisor for Batch Release at ProKidney Corp. Since 2023, Amanda has been responsible for managing drug product dispositions and ensuring compliance with regulatory requirements in a cGMP manufacturing environment. With prior experience as a Global Regulatory Affairs Specialist at Market America, Inc. from 2016 to 2021, and various roles at Hospira and BestCo, Amanda has developed extensive expertise in batch record review, deviation management, and team training. Amanda holds a Bachelor of Science in Biology from Elizabeth City State University, which was obtained in 2009.
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