Jobs at AbCellera

The job focuses on expanding teams in Protein Science, Drug Development, Manufacturing, Quality, and supporting roles in various scientific and engineering fields.

Leads QA Operations for a biological drug substance clinical manufacturing facility, providing GMP oversight across manufacturing, warehousing, and distribution. Responsibilities include batch record review, material disposition, investigations, CAPAs, change controls, tech transfers, audits, inspection readiness, risk management, continuous improvement, and regulatory compliance. Builds and coaches the QA team while partnering with manufacturing, supply chain, regulatory, QC, MSAT, and logistics stakeholders.

Oversee IT systems supporting drug discovery, modernize infrastructure, mentor team members, and lead technical projects in both cloud and on-prem environments.

The Systems Administrator will manage cloud and on-prem infrastructure, troubleshoot issues, support internal tools, and automate operations to improve efficiency.

Support FP&A for preclinical and clinical asset portfolio: build long-range forecasts, monthly management reporting, valuation and business-case modeling, partner with cost centers and senior leaders, improve data workflows and forecasting processes, and provide analyses to inform strategic decision-making.

Lead multi-jurisdictional payroll and equity operations across Canada, the U.S., and Australia. Manage bi-monthly and off-cycle payroll runs, tax filings, reconciliations, shadow payrolls, payroll journal entries, and year-end reporting. Administer equity programs (RSUs, options, ESPP), respond to employee pay/equity inquiries, and collaborate with Finance, Accounting, Legal, and People teams to ensure accurate pay data and compliance with grants and contracts.

Lead GMP QC microbiology operations for DS clinical manufacturing and external partners. Own contamination control, environmental and utilities monitoring, microbial methods, troubleshooting, investigations, data integrity (ALCOA++), team mentorship, audit readiness, and SOP governance to ensure compliant testing and timely product release.

Diriger la conception, la planification et la supervision detudes de toxicologie non clinique (GLP et non-GLP) pour soutenir le dvelop pent clinique et reglementaire; assurer la liaison scientifique avec les CROs; reprsenter l'innocuit non clinique auprs des programmes, realiser des evaluations scientifiques et prrecommendations claires pour orienter la stratgie clinique et rgulementaire.

Partner with teams as a trusted coach on engagement, development, performance, and hiring. Deliver company-wide HR initiatives, maintain people data in Bamboo, advise managers on compensation and performance, surface team insights to People & Culture, and support recruiting and organizational design.