FDA-licensed plasma fractionation and source collection for immune globulin therapies
ADMA Biologics manufactures three FDA-approved plasma-derived immune globulins (BIVIGAM, ASCENIV, NABI-HB) and operates both a fractionation facility and source plasma collection network. The company's tech stack and project backlog are operationally focused—SAP implementations, process validation, and cGMP compliance dominate—with manufacturing roles outnumbering engineering 6.5-to-1, signaling a capital-intensive, regulated-manufacturing business rather than a software or R&D startup.
Notable leadership hires: Regional Business Director
ADMA Biologics is a public, end-to-end biopharmaceutical manufacturer headquartered in Ramsey, NJ with core operations in Boca Raton, FL. The company manufactures and markets three FDA-approved plasma-derived biologics for immunodeficient and at-risk populations. It operates an FDA-licensed plasma fractionation and purification facility in Boca Raton and runs ADMA BioCenters, a subsidiary that collects source plasma for use in its own manufacturing. The company targets niche immunology and infectious disease markets, serving immunocompromised patient populations. With 501–1,000 employees and active hiring across manufacturing, healthcare, and operations roles, ADMA is scaling production and compliance infrastructure.
ADMA manufactures three FDA-approved plasma-derived immune globulins: BIVIGAM for primary humoral immunodeficiency, ASCENIV (10% liquid formulation) for immunodeficiency treatment, and NABI-HB for hepatitis B immunity. All products are produced at its FDA-licensed fractionation facility in Boca Raton, Florida.
ADMA Biologics is headquartered in Ramsey, NJ, with primary manufacturing and plasma collection operations based in Boca Raton, Florida.
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