FDA-licensed plasma collection and specialty biopharmaceutical manufacturing
ADMA BioCenters operates FDA-licensed plasma donation facilities as a wholly-owned subsidiary of ADMA Biologics, a biopharmaceutical manufacturer focused on plasma-derived therapeutics for infectious disease prevention. The hiring mix is heavily weighted toward manufacturing (27 roles) and healthcare (23 roles) with acute focus on compliance, validation, and operational scaling—reflected in active projects spanning cGMP standardization, facility validation, and training curriculum rollout. Pain points cluster around SOP adherence, donor workflow efficiency, and equipment validation, suggesting a maturing manufacturing operation scaling compliance infrastructure.
Notable leadership hires: Business Director
ADMA BioCenters collects human plasma from donors at FDA-licensed facilities, which serves as the raw material for ADMA Biologics' specialty plasma-derived medications targeting infectious disease treatment in immunocompromised and at-risk populations. The company operates a 201–500-person organization headquartered in Roswell, Georgia, structured primarily around manufacturing, healthcare operations, and regulatory functions. Current operational priorities center on quality systems modernization (cGMP initiatives, SOP revision), facility and equipment validation, and month-end financial close optimization. Tech stack leans on SAP for enterprise resource management, LIMS and HPLC for laboratory workflows, and standard office and documentation tools.
ADMA BioCenters operates FDA-licensed plasma collection facilities that supply human plasma to ADMA Biologics for manufacturing specialty plasma-derived medications to treat and prevent infections in immune-compromised patients.
Core systems include SAP (enterprise resource planning), LIMS and HPLC (laboratory information and analytical instrumentation), Blackline (financial close), and GCP cloud infrastructure, alongside standard Microsoft Office and SharePoint.
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