Todd Mabe

Todd Mabe is a Vice President of Good Manufacturing Practice at Akouos, inc. His oversight includes the disposition of internal and external manufactured clinical goods. His team ensures that quality expectations are met for establishing clinical specifications, clinical protocols, deviation management, change management, lot release, CAPA, risk management, regulatory filings, and inspections. He is a member of the leadership team that develops and executes Merck's future clinical strategy. His past experiences in the biotech and pharmaceutical industries include QC release testing and quality management. He has been a validation manager and a quality consultant. He has experience in establishing and maintaining quality systems for validation, document management, change control, discrepancy management, training, validation document strategic development, execution and approval; analytical method validation; and the engineering of pharma and biotech facilities