Apply GMP quality control expertise at OmniaBio, supporting cell and gene therapy manufacturing through testing, data review, and sample management.
As an Associate II, Quality Control, you will support clinical translation in cell therapy and regenerative medicine. You will work across method development, equipment qualification, stability programs, and QC documentation. The position requires collaboration with Production, MSAT, and QA teams to deliver compliant contract services.
Key Responsibilities: Perform material testing across incoming, in-process, drug substance, and drug product materials
Manage samples, stability programs, equipment, and reference standards
Develop, optimize, qualify, and validate QC methods
Review data and completed records for GMP compliance
Support client,



internal, supplier, and health authority audits
Requirements: Bachelor’s degree in science; master’s degree preferred
Four to six years supporting GMP cell therapy quality control
Experience within a CDMO, testing facility, biotechnology, or similar company
Robust understanding of cell manufacturing processes and technologies
Excellent knowledge of Health Canada and FDA GMP regulations
Bring cell therapy QC, GMP compliance, and analytical expertise to OmniaBio’s regenerative medicine manufacturing services.

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📌 GMP Cell Therapy Quality Control Associate (Ontario)
🏢 Centre for Commercialization of Regenerative Medicine
📍 Ontario