Bryan Lisa is a senior global QRC leader specializing in the medical device, pharmaceutical, and biologics sectors. They currently serve as the Sr. Director of MedTech Regulatory Operations at Johnson & Johnson, leveraging extensive experience in regulatory affairs and quality systems. Previously, Bryan held positions as Director of WW Regulatory Affairs at Ortho Clinical Diagnostics and Associate Director of Regulatory Affairs at Johnson & Johnson, contributing to significant projects such as leading carve-out efforts and managing international registrations. Bryan also has a strong educational background in Quality & Manufacturing Management and Biology from Penn State University, along with executive training in Regulatory Affairs from Northwestern University. They are recognized for building high-performing teams and driving compliant, innovative strategies in a highly regulated industry.
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