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 Director will provide strategic leadership for the development, verification, and commercialization of drug-device combination products like pre-filled syringes and autoinjectors. They will oversee cross-functional teams and external partners to ensure regulatory compliance and successful product launch.
On-site · Vancouver
Lead the planning, authoring, and execution of global CMC regulatory submissions for biologics programs from pre-clinical to commercialization. Provide strategic guidance and review technical documentation to ensure compliance with global health authority requirements.
On-site · Vancouver
The Senior CMC Regulatory Affairs Manager will lead the planning, authoring, and execution of global CMC regulatory submissions for biologics programs. They will also provide strategic guidance to cross-functional teams to ensure compliance with global health authority requirements.
On-site · Vancouver
The Research Scientist will execute bioanalytical and pharmacokinetic activities to support antibody therapeutic programs, specifically focusing on T-cell engager projects. They will collaborate with cross-functional teams to define PK strategies and drive the development of innovative bioanalytical methods.
On-site · Vancouver
The intern will provide technical support to employees by managing hardware, software, and user accounts while troubleshooting system and network issues. They will also maintain IT inventory and assist senior staff with various ad hoc projects.
On-site · Vancouver
The intern will provide technical support to employees via ticketing systems and in person, while managing user accounts and hardware. Responsibilities include configuring new computers, maintaining IT inventory, and troubleshooting system and network failures.
On-site · Vancouver
The Director will lead the drug safety and pharmacovigilance framework, managing external partners and ensuring regulatory compliance for clinical programs. They will oversee safety data review, signal detection, and the preparation of periodic safety reports for global regulatory submissions.
On-site · Vancouver
The Regulatory Submissions Specialist will lead the electronic publishing, formatting, and compilation of clinical development submissions to ensure compliance with global regulatory standards. They will coordinate publishing projects, perform quality checks, and manage submission documentation while optimizing internal workflows.
On-site · Vancouver
Lead the electronic publishing, formatting, and compilation of clinical development submissions to ensure compliance with global health authority requirements. Coordinate publishing projects with internal stakeholders and perform rigorous quality checks to maintain high submission standards.
On-site · Vancouver
The role involves steering delivery device strategy for drug-device combination programs and architecting design control frameworks. You will lead strategic supplier partnerships and ensure device development meets regulatory and quality standards from design intent to clinical reality.
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.
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 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 · 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.
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
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.
