Description
OmniaBio is hiring an Associate I, Quality Assurance (QA) to support GMP manufacturing of cell and gene therapy products. The role covers manufacturing quality, product release, batch documentation, metrics, audits, deviations, corrective and preventive actions, change controls, quality systems, document control, training, vendor management, and regulatory inspections. The position requires a high school diploma with additional college courses in science or engineering, 1–2 years of experience in cell therapy or viral quality supporting GMP production, and knowledge of Health Canada or U.S. FDA GMP regulations and QA principles.
