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Adverum Biotechnologies, Inc. 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. Adverum is looking for a QA Manager, Document Control reporting to the Sr. QA Manager, Master Control Project Administrator. In this role you will perform various duties essential to the maintenance and/or support of Document Control and Adverum’s quality systems including System Administration of MasterControl EQMS, training, deviations, CAPAs, Change Control, Lot Disposition, Product Complaints, and other duties as assigned by Adverum’s QA department.
