Key Responsibilities: The QC Program Implementation Lead will establish Sabin's first dedicated QC capability by designing and implementing a phase-appropriate, current Good Manufacturing Practice (cGMP)-compliant QC framework that supports the transition from Phase 2 through Phase 3, Process Performance Qualification (PPQ), Biologics License Application (BLA), and commercialization. Support regulatory and US Government (USG) submissions, audits, and inspections by ensuring that QC data and supporting records are complete, accurate, attributable, traceable to source documentation, appropriately reviewed, and consistent across analytical reports, certificates of analysis, stability reports, regulatory submissions, and other required deliverables.