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company in Vancouver, Canada
Each of us cares about someone who will need medicines. That’s why our vision is to repeatedly beat the odds to deliver breakthrough medicines to patients that need them. We pursue truth and scientific rigour and have…
Each of us cares about someone who will need medicines. That’s why our vision is to repeatedly beat the odds to deliver breakthrough medicines to patients who need them. We pursue truth and scientific rigour and have…
Clinical Systems Analyst at AbCellera (Montreal) supporting clinical trial system implementations and sustainment: day-to-day user training/support, creating and executing GxP validation test scripts, and coordinating vendors on configuration and releases for systems like RTSM, EDC, and eCOA, bridging Clinical Operations, Digital Quality, and IT.
AbCellera is hiring a QA for QC Specialist in Vancouver on a 15-month contract to review and disposition data from cGMP Quality Control labs supporting biologics clinical manufacturing — approving protocols, handling deviations/CAPAs/OOS results, and supporting inspections and regulatory submissions. Requires a science degree, 3-5+ years of QA/QC biotech experience, and strong cGMP/regulatory know
QA Specialist at AbCellera (Vancouver) performs cGMP compliance and accuracy reviews of executed Batch Production Records, logbooks, and electronic records for clinical antibody-drug batches made in-house and at CDMOs, supporting batch disposition. Core work involves GDP/ALCOA++ documentation review, ERP materials release, quality events (deviations, CAPAs), and inspection readiness.
A 15-month contract QA Operations Specialist at a clinical-stage biotech in Vancouver: you review GMP batch records, raw data, and quality events (deviations, CAPAs, change controls), release materials in the ERP, and support audits and inspections to keep clinical manufacturing cGMP-compliant and inspection-ready.
AbCellera is hiring an External QA Specialist/Manager in Vancouver to oversee the quality of contract manufacturers (CMOs) producing its monoclonal antibody drugs — handling supplier qualification, quality agreements, batch record review/disposition, GMP audits, and inspection readiness. Core focus is biopharma cGMP quality management using eQMS/enterprise tools like Veeva and SAP.
QA Specialist on AbCellera's Supplier Quality Management team overseeing the full supplier lifecycle — selection, qualification, quality agreements, deviations, risk assessments, and audit readiness — for materials and services supporting monoclonal antibody programs. Requires QA experience in regulated biopharma, cGMP knowledge, and eQMS/ERP tools like Veeva and SAP.
Senior Systems Engineer designs, builds, and maintains hybrid cloud and on-prem IT systems for a biotech company’s drug discovery pipeline, using automation and infrastructure-as-code to improve reliability and efficiency.
Maintains and improves a hybrid IT environment (AWS cloud and on-prem) for a biotech company, troubleshooting systems, automating operations, and partnering with scientists and engineers.
Partner with teams at a biotech company to coach managers, improve engagement, and shape HR policies, using tools like BambooHR and data-driven insights.
Leads Quality oversight for biological drug manufacturing in Vancouver, ensuring GMP compliance, operational excellence, and team development while partnering with manufacturing, supply chain, and regulatory teams.