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Vanessa Smiley is currently serving as the Associate Director of Dose Preparation & Supply Chain Quality Assurance at BlueRock Therapeutics since January 2024. With a diverse background in quality assurance and regulatory compliance, Vanessa has held multiple roles, including Freelance Blogger focusing on patient advocacy for sleep disorders at Health Union, and Senior Consultant at Azzur Group. Previous positions include Manager of External Quality Assurance at Verve Therapeutics, where responsibilities involved managing external vendors related to drug candidates, and GMP Operational Quality Senior Specialist at Vertex Pharmaceuticals, overseeing quality for cystic fibrosis drugs. Earlier experience includes roles at Lonza and Eisai US, along with a brief period in financial services. Vanessa holds a Master of Science in Chemistry/Biochemistry from Youngstown State University and has completed courses in Regulatory Sciences at The Johns Hopkins University.