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 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 · Montréal
Plan, lead, and oversee international clinical studies from inception to closure, ensuring compliance with regulatory requirements and protocols. Collaborate with cross-functional teams to generate high-quality clinical data while managing budgets and timelines.
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
Lead the design, planning, and supervision of non-clinical toxicology studies to support regulatory filings for biologics. Act as the primary scientific liaison with CROs and provide toxicological expertise to cross-functional drug discovery and development teams.
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 oversee and execute in vivo studies, ensuring high standards of animal welfare and compliance with regulatory protocols. They will collaborate with cross-functional teams to support antibody discovery through technical expertise, data recording, and laboratory maintenance.
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 Clinical Study Manager will lead and manage clinical trials from start-up through completion, ensuring efficient and timely execution in compliance with regulations, protocols, and SOPs. This involves overseeing global strategy, managing timelines and budgets, identifying risks, and ensuring data quality and participant safety.
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.
On-site · Vancouver
Lead the medical strategy for clinical development programs in endocrinology and autoimmune diseases, ensuring safety and regulatory compliance. Oversee the design, execution, and reporting of clinical trials while collaborating with cross-functional teams.
On-site · Vancouver
Lead the design and oversight of in vitro and in vivo toxicology studies to assess the safety of drug candidates. Serve as a subject matter expert for nonclinical safety, authoring regulatory documentation and providing risk-benefit evaluations to leadership.
On-site · Vancouver
Operate and maintain a hybrid IT infrastructure consisting of AWS cloud and on-prem systems to support scientific and engineering teams. Automate routine operational tasks and ensure the availability and efficiency of platforms used for drug discovery and development.
On-site · Vancouver
Perform daily animal health assessments, cage changes, and maintain the cleanliness and organization of the in vivo facility. Support the discovery of therapeutic antibodies by preparing lab materials and managing sample shipments.
On-site · Vancouver
The Payroll Administration Manager will oversee multi-jurisdictional payroll and equity functions across Canada, the US, and Australia. Responsibilities include managing payroll cycles, tax filings, and equity administration while ensuring accuracy and compliance.
On-site · Montréal
You will lead the planning, design, implementation, and interpretation of non-clinical toxicology programs to support drug development. This includes liaising with contract research organizations and representing the non-clinical safety department in cross-functional teams.
On-site · Vancouver
The Research Scientist II will design, plan, and execute toxicology studies to assess the safety of drug candidates. They will also maintain study data and collaborate with various teams to ensure high data quality.
