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 (Winnipeg)
🏢 Centre for Commercialization of Regenerative Medicine
📍 Winnipeg