Description
OmniaBio is hiring an Associate I, Quality Control to support GMP manufacturing of cell and gene therapy products. The role covers sample management, material and environmental testing, method development and optimization, equipment qualification and validation, stability programs, data review, audits, deviations, change controls, and GMP compliance. The position requires a high school diploma, preferably a college diploma, 1–2 years of experience in cell therapy or viral quality control supporting GMP production, and experience in a CDMO, third-party testing facility, or biotechnology company.
