Gmp Cell Therapy Quality Control Associate

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 materialsManage samples, stability programs, equipment, and reference standardsDevelop, optimize, qualify, and validate QC methodsReview data and completed records for GMP complianceSupport client, internal, supplier, and health authority auditsRequirements:
Bachelor’s degree in science;
master’s degree preferredFour to six years supporting GMP cell therapy quality controlExperience within a CDMO, testing facility, biotechnology, or similar companyStrong understanding of cell manufacturing processes and technologiesExcellent knowledge of Health Canada and FDA GMP regulationsBring cell therapy QC, GMP compliance, and analytical expertise to OmniaBio’s regenerative medicine manufacturing services.
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