OmniaBio: Associate Quality Assurance; MQA)

Omnia Bio:
Associate I Quality Assurance (MQA)

Hamilton, ON, Canada

Posted Friday, August 7, 2026 at 4:00 AM

About Omnia Bio:

Omnia Bio Inc. is a technology-driven, global CDMO specializing in cell and gene therapies, with a mission to transform biomanufacturing with AI and automation. Located at McMaster Innovation Park in Hamilton, Ontario, Omnia Bio leverages over a decade of expertise in regenerative medicine and advanced therapies developed in partnership with CCRM. Committed to digital transformation, Omnia Bio integrates automation, robotics, and artificial intelligence into its operations to drive efficiency, enhance quality, and increase throughput.

This innovative approach supports end-to-end CDMO services—from development through GMP manufacturing and scale‑up—helping clients accelerate the path to market for transformative treatments. Omnia Bio focuses on immune cell‑based therapies, induced pluripotent stem cell therapies, and lentiviral vectors, positioning itself as a leader in advancing and maturing cell and gene therapy manufacturing. With a strategic vision to meet the surging global demand, Omnia Bio aims to enable broad access to cutting‑edge therapies worldwide.  

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Active Vacancy

As Associate I, Quality Assurance (QA),at Omnia Bio, you are a motivated individual in the field of Good Manufacturing Practices (GMP) manufacturing of cell and gene therapy products whoisdriven by the opportunity to enable clinical translation of cell therapy and regenerative medicine. The QA teamis responsible forall aspectsof GMP for the organization and the AssociateI,QA,willbe required to work across the entire range of activities, including, but not limited to,quality system management,manufacturing quality,and outsourced activities.

You will demonstrate flexibility within the QA teamand larger organization,navigating work priorities,as required.

Youwill ensure the high‑quality delivery of contract services.

• Delivers quality‑related services including product release, as contracted, to various cell and viral product‑centered clients.
• Prepares the master batch documentation and specification systems, as required.
• Prepares metrics and trend data.
• Provides in‑suite and on‑the‑floor support for Omnia Bio’s manufacturing teams, ensuring compliance with a fast‑to‑patient mindset.
• Prepares the release of packages for approval.
• Reviews completed batch records and associated records to ensure GMP compliance and collaborates with colleagues on the Manufacturing and the Manufacturing Science and Technology (MSAT) teams to remedynon‑compliance.
• Participates in internal audits, supplier audits, or regulatory inspections as required.
• Administers documentation and training programs to the organization.
• Supports the vendor management program.
• Supports quality systems, as required.
• Prepares and manages deviations, corrective and preventive action, change controls, etc.
• Collaborates with Manufacturing, MSAT, Quality Control (QC) and QA leadership in the preparation of master batch record and specifications.
• Participates in internal, client and health authority audits, as required.
• Collaborates with Facilities/Engineering to ensure that facilities are available for production, including, but not limited to, room readiness, calibration and maintenance activities.
• Supports validation in the collaboration, review and approval of master qualification protocols, executed protocols, and summary reports.
• Ensures GMP is embedded in all manufacturing‑related tasks.
• Engages and supports the Omnia Bio Operating Model continuous improvement philosophy.

• Delivers quality‑related services to various cell and viral…