Teams at SAB Biotherapeutics

Leads analytical development for biologics programs from early development through commercialization. Responsibilities include hands-on method development, optimization, qualification, validation, transfer, lifecycle management, troubleshooting, investigations, stability and reference standard programs, and regulatory submission support. Ensures cGMP, data integrity, ICH, USP, and regulatory compliance while supporting CMC milestones, laboratory operations, equipment qualification, LIMS implementation, external partners, and inspection readiness.

Leads analytical development and quality control strategy for biologics from early development through commercialization. Oversees method development, validation, transfer, lifecycle management, troubleshooting, investigations, reference standards, critical reagents, comparability, and regulatory CMC submissions. Provides hands-on laboratory leadership, manages internal teams and external partners, ensures cGMP and regulatory compliance, supports inspection readiness, and scales analytical capabilities, equipment, workflows, and LIMS infrastructure.

Leads SAB’s Program Management function and serves as senior program leader for SAB-142 through late-stage biologics development, BLA submission, regulatory review, approval, and launch readiness. Oversees cross-functional execution across clinical, regulatory, CMC, manufacturing, quality, supply chain, finance, and commercial teams. Establishes governance, integrated plans, budgets, risk mitigation, and executive reporting while managing external partners. Builds and develops the Program Management organization and supports commercial readiness, strategic partnerships, and alliance activities.