UPLC, ELISA, and qPCR expertise can support AbCellera’s cGMP Quality Control laboratories and clinical manufacturing of biologics. Deliver accurate, timely analytical results.
As a QC Analyst II, you will perform analytical and immunochemical testing for biologics drug substance and drug product. You will support method lifecycle activities, release and stability testing, clean utility monitoring, raw material testing, and laboratory readiness. Your work supports clinical-stage therapies.
Key Responsibilities: Perform UPLC, CE-SDS, icIEF, ELISA, qPCR, and UV-Vis testing
Execute release, stability, in-process, and raw material testing
Support analytical method development, verification, qualification, and validation
Review data and escalate suspect or atypical results




Author controlled QC documents, protocols, reports, and work instructions
Requirements: Bachelor’s degree with five-plus years of QC experience
Master’s degree with three-plus years of QC experience
Robust GMP, data integrity, and analytical QC knowledge
Hands-on immunochemical and physicochemical testing experience
Experience with LIMS and chromatography data systems
Apply analytical rigor, GMP knowledge, and biologics testing experience to QC work supporting AbCellera’s clinical-stage medicines.

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📌 QC Analyst II Biologics Testing (British Columbia)
🏢 Peptide Atlas
📍 British Columbia