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.

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