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 scientist will develop and optimize separations-based analytical methods to support monoclonal antibody CMC programs and product characterization. They will also collaborate with technical teams to provide guidance, interpret data, and contribute to regulatory submissions.
On-site · Vancouver
Provide quality oversight for Contract Manufacturing Organizations (CMOs) throughout the full lifecycle, including qualification, batch manufacturing, and compliance. Act as a Person-in-Plant during manufacturing campaigns to ensure GMP compliance and perform risk-based quality assessments.
On-site · Vancouver
You will provide quality oversight for suppliers throughout the full lifecycle, including selection, qualification, and ongoing management. Additionally, you will manage quality events, perform risk assessments, and ensure compliance with regulatory standards during audits.
On-site · Vancouver
Perform analytical and immunochemical testing to support clinical manufacturing of biologics drug substances and products. Manage method lifecycle activities, stability testing, and laboratory readiness while ensuring compliance with GMP standards.
On-site · Vancouver
The Senior QC Data Reviewer will perform independent GMP reviews of analytical and microbiological data to ensure accuracy, traceability, and compliance with regulatory standards. They will partner with scientists to resolve documentation gaps and support the timely release of clinical products.
On-site · Vancouver
The Senior Manager will lead the QC Microbiology function, providing strategic direction and technical oversight for internal operations and external testing partners. They are responsible for the site's contamination control program, team development, and ensuring compliance with GMP requirements.
On-site · Vancouver
<p>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 the courage to work at the edge of the unknown. </p> <p>We are looking for an enthusiastic QA for QC Specialist to join our Quality Assurance Operations team and help ensure the quality and compliance of the data behind our biologics clinical manufacturing. In this role, you'll review and disposition the data generated from the cGMP Quality Control (QC) labs, which support our…
On-site · Vancouver
<p>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 the courage to work at the edge of the unknown. </p> <p>We're looking for an enthusiastic QA Specialist to join our Quality Assurance team and help ensure our clinical batches meet the highest standards of cGMP compliance. In this role, you'll conduct comprehensive compliance reviews of executed Batch Production Records (BPRs) and related manufacturing documentation for batche…
On-site · Vancouver
<p>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 the courage to work at the edge of the unknown. </p> <p>We're looking for an enthusiastic QA Operations Specialist to join our Quality Assurance Operations team on a 15-month contract and help ensure our clinical batches meet cGMP standards. In this role, you'll support the compliance of our manufactured and tested clinical batches by authoring, reviewing, and maintaining the…
On-site · Vancouver
<p>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 the courage to work at the edge of the unknown.</p> <p>We are looking for a VP, Medical Affairs to join our team to build and provide overall leadership for the Medical Affairs function, including executing on Medical Affairs priorities and investigator initiated activities, supervising field Medical Science Liaisons, overseeing clinical and scientific publications, and devel…
On-site · Vancouver
The Director will define and lead the Manufacturing Sciences and Technology strategy for biological drug products, serving as the senior technical authority for external manufacturing partners. Responsibilities include overseeing technology transfers, ensuring cGMP compliance, managing batch documentation, and driving process performance improvements.
On-site · Vancouver
<p>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 the courage to work at the edge of the unknown. </p> <p>We are looking for a highly motivated and detail-oriented Associate Research Scientist to join our In Vivo Pharmacology team. Working hands-on in the lab alongside experienced pharmacologists, you’ll help build the foundation of scientific rigour that our programs are built on. You’ll support the preparation and analytic…
On-site · Vancouver
The Research Scientist will design, execute, and analyze in vivo pharmacology studies to support drug candidate selection and pipeline advancement. They will also collaborate with cross-functional teams to develop novel animal models and mentor junior scientists in experimental methodologies.
On-site · Vancouver
The VP of Medical Affairs will build and lead the Medical Affairs function, overseeing strategy, team development, and scientific communication. They will partner with cross-functional teams to support prelaunch and postlaunch activities while managing key opinion leader relationships and clinical data dissemination.
On-site · Vancouver
Lead the late-stage manufacturing science and technology function to transition antibody-based biologics from clinical manufacturing to commercial readiness. Oversee process characterization, regulatory submissions, and cross-functional alignment with internal teams and CDMO partners.
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
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 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.
