Specialist III, QA Operations (Contract)

Adverum Biotechnologies, Inc., wholly owned subsidiary of Eli Lilly and Company, is a mission-driven clinical-stage company that aims to establish gene therapy as a new standard of care for highly prevalent ocular diseases with the aspiration of developing functional cures to restore vision and prevent blindness. Leveraging the research capabilities of its proprietary intravitreal (IVT) platform, Adverum is developing durable, single-administration therapies designed to be delivered in physicians’ offices to eliminate the need for frequent ocular injections to treat these diseases. By overcoming the challenges associated with current treatment paradigms for these debilitating ocular diseases, Adverum aspires to transform the standard of care, preserve vision, and create a profound societal impact around the globe.   Note to Recruiters and Agencies All recruiter and agency inquiries must go through Adverum’s internal Talent Acquisition team.  Unsolicited resumes sent to Adverum will be considered Adverum's property.   Adverum’s Talent Acquisition team must expressly engage agencies for any requisition.  Direct contact with hiring managers by agencies will not be tolerated and may affect your ability to work with Adverum in the future.   Adverum is looking to hire a Specialist III, QA Operations (Contract), is responsible for leading and executing quality assurance activities required for the disposition of cell and viral banks/drug substance/drug product lots. This position ensures that all manufacturing, testing, stability and related quality documentation from internal operations, contract manufacturing organizations (CMOs), and contract testing laboratories (CTLs) is reviewed for accuracy, completeness, and compliance with current Good Manufacturing Practices (cGMP), regulatory requirements, and company quality standards. The Specialist verifies that all quality data—whether generated in-house or externally—is acceptable for lot release and/or Regulatory submission, and ensures that deviations, change controls, investigations, and other quality events are resolved in accordance with established procedures. This position collaborates cross-functionally with Manufacturing, Quality Control, Supply Chain, Regulatory Affairs, and external partners to ensure timely and compliant lot disposition in support of clinical and commercial programs.