Teams at SAB Biotherapeutics

Lead manufacturing strategy and execution for late-stage clinical and commercial biologics supply. Oversee CDMO partnerships, technology transfer, scale-up, process validation, GMP operations, CMC documentation, regulatory readiness, supply planning, and build a high-performing Technical Operations organization.

Execute and validate bioanalytical and ligand-binding immunoassays, perform PK analysis of clinical samples, maintain electronic lab notebooks, ensure GCLP compliance, support regulatory documentation, and manage general laboratory operations.

Lead and scale global Quality Assurance to support transition from late‑stage clinical development to commercialization. Own GxP compliance, quality systems, clinical and CMC quality oversight, supplier and manufacturing quality, inspection readiness, and responses to regulatory observations. Partner cross‑functionally to ensure timely release of clinical materials and regulatory submission readiness while building a high‑performing QA team and driving continuous improvement.