Abbott
Quan Le has over 17 years of experience in quality management and engineering, currently serving as Quality Manager and Principal Quality Engineer at Abbott Laboratories since June 2006. Responsibilities include overseeing IQA/IQC, CAPA, and compliance, as well as leading global strategic sourcing and supply chain development initiatives. Previous roles include Principal Supplier Development and Quality Engineer and Sr. Supplier Quality Engineer at Abbott, where expertise was applied in manufacturing processes and regulatory compliance for medical devices. Prior experience includes positions as Process Development Engineer at J&J and SiPix Imaging, focusing on process development and optimization for drug delivery systems and polymer formulations. Quan Le earned a Bachelor of Sciences in Chemical Engineering and Materials Science Engineering from the University of California, Davis.
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