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
- Solid 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.

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