Our platform integrates biology, computation, and engineering to develop impactful antibody-based medicines.
Vancouver, British Columbia
AbCellera is a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology.
On-site · Vancouver
The Senior Manager/Associate Director will provide real-time quality oversight for biological drug substance manufacturing, warehousing, and distribution operations. They will lead root cause investigations, manage CAPAs, and ensure site-wide compliance with regulatory standards and internal quality policies.
On-site · Vancouver
Lead quality oversight for biological drug substance clinical manufacturing, including batch record review, material disposition, and regulatory compliance. Manage root cause investigations, CAPAs, and change controls while coaching a high-performing QA operations team.
On-site · Montréal
The Clinical Study Start-Up Manager will oversee the execution of all start-up activities, including site selection, qualification, and activation. They will manage essential documentation, regulatory submissions, and contract negotiations to ensure clinical trials proceed efficiently and in compliance with GCP standards.
On-site · Montréal
The Clinical Project Manager will lead cross-functional teams to execute clinical trials and ensure alignment with global regulatory and supply goals. They are responsible for managing site-level execution, identifying high-performing research sites, and navigating regional ethics landscapes.
On-site · Montréal
The Clinical Research Coordinator will support the management of clinical trials throughout their lifecycle, ensuring compliance with regulatory requirements and Good Clinical Practice. Responsibilities include maintaining trial documentation, coordinating meetings, managing logistics, and facilitating communications between clinical sites and vendors.
On-site · Montréal
The Clinical Trial Coordinator will support the management of clinical trials from initiation to close-out, ensuring compliance with regulatory requirements and Good Clinical Practice. Responsibilities include maintaining trial documentation, coordinating meetings, handling logistics, and assisting with trial-related communications.
On-site · Vancouver
The Associate Scientist will support pre-formulation and formulation development studies for antibody-based drug products, including conducting biophysical characterization and stability testing. They will also assist in small-scale fill-finish activities and maintain accurate laboratory records in compliance with data integrity standards.
Hybrid · Montréal
The Clinical Study Manager will lead and oversee global clinical trials from start-up to completion, ensuring compliance with protocols and regulatory standards. They will collaborate with cross-functional teams to manage timelines, budgets, and data quality while monitoring participant safety.
On-site · Montréal
The Senior Clinical Research Associate serves as the primary link between the company and investigative sites, ensuring patient safety, data integrity, and regulatory compliance. They manage a portfolio of complex sites, overseeing the full spectrum of monitoring activities from selection to close-out.
On-site · Vancouver
The Finance Analyst will maintain long-range operating forecasts and projections while collaborating with project teams to support strategic decision-making. They will also generate valuation analyses, manage monthly reporting, and build business cases for new initiatives.
On-site · Vancouver
The Finance Analyst will support strategic decision-making by maintaining long-range operating forecasts and projections for preclinical and clinical assets. They will partner with leaders to manage operating plans, generate data-driven insights, and improve data workflows and valuation models.
On-site · Vancouver
The QC Microbiology Manager leads laboratory operations, contamination control programs, and microbiological testing strategies at a GMP manufacturing facility. This role provides technical mentorship, oversees external testing, and ensures all microbiological data and processes comply with regulatory standards.
On-site · Vancouver
The Principal Scientist will lead the planning, design, and execution of non-clinical toxicology programs to support regulatory submissions and candidate development. They will serve as the primary scientific interface with CROs and provide expert toxicology guidance to cross-functional teams.
Hybrid · Montréal
The Principal Scientist will lead the design, execution, and interpretation of nonclinical toxicology programs to support global regulatory submissions. They will serve as the primary scientific interface with contract research organizations and provide expert safety assessments for cross-functional development teams.
On-site · Vancouver
Act as a trusted coach and strategic partner to teams, focusing on employee development, performance management, and role progression. Support company-wide People & Culture initiatives and manage people data within the Bamboo platform.
On-site · Vancouver
The role involves designing and executing in vitro and in vivo toxicology studies to assess the safety of drug candidates. Responsibilities include maintaining GLP-compliant data and authoring toxicology sections for regulatory documentation.
On-site · Vancouver
Manage end-to-end multi-jurisdictional payroll and equity functions across Canada, the US, and Australia. Oversee tax filings, GL reconciliations, and provide support for equity compensation programs and employee inquiries.
On-site · Vancouver
Own and evolve the IT systems supporting drug discovery and development pipelines across hybrid cloud and on-prem environments. Lead the modernization of infrastructure through automation, infrastructure-as-code, and technical mentorship of other engineers.
On-site · Vancouver
The In Vivo Specialist will perform in vivo and ex vivo techniques to support therapeutic antibody discovery and efficacy assessments. They are responsible for maintaining high standards of animal welfare, accurate data documentation, and ensuring efficient study execution.
On-site · Vancouver
The company is seeking top talent to expand its teams, with current hiring focus areas including Protein Science, Drug Development, Manufacturing, and Quality. They are also interested in candidates who can contribute to supporting functions like Translational Biology, Engineering, Bioinformatics, Machine Learning, IT, Laboratory Management, and Software Development.
