Lisa O'Brien is an Associate Director in Regulatory Affairs International at Merck, where they have supported international regulatory submissions for vaccines, including GMO vaccines, since 2017. With extensive experience in vaccine manufacturing, testing, and Quality Assurance, Lisa has a proven track record of managing complex programs and obtaining necessary approvals from Health and GMO Authorities globally. Prior to this role, they served as a Senior Scientist and held multiple positions within Merck from 2015 to 2017. Lisa holds a Bachelor of Science in Biology from Delaware Valley University.
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