Michael Liss is the Associate Director of Quality Systems & Compliance at Merck, where they lead a team focused on improving quality systems and enhancing operational efficiency. Their extensive experience in biopharmaceutical manufacturing includes roles as a Validation Engineer at companies such as Amgen and Genzyme, where they contributed to significant projects involving compliance and process optimization. Michael's earlier work included positions at Talecris and CNH, where they honed their skills in validation and engineering. Currently, they are pursuing a Bachelor of Science in Mechanical Engineering at the University of Illinois at Chicago.
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