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AbCellera

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Our platform integrates biology, computation, and engineering to develop impactful antibody-based medicines.

Vancouver, British Columbia

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Biotechnology Research
501–1,000 people

About

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.

Open positions

Senior Clinical Scientist

On-site · Vancouver

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. We are seeking an experienced Senior Clinical Scientist to join our growing Clinical Development team, to drive early-phase development in oncology and endocrinology indications. Reporting to VP of Clinical Development and in collaboration with a Medical Director, you will integrate preclinical findings into clinical strategies a…

Associate Director, Regulatory Affairs

On-site · Vancouver

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. We are looking for a Regulatory Affairs (RA) leader to join our growing team. You will implement global regulatory strategies and develop CTA/IND submissions across AbCellera’s portfolio of innovative biologics-based therapeutics. As the primary point of contact with regulatory authorities, you will also provide expert regulatory…

Senior Medical Writer

On-site · Vancouver

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. We are looking for a skilled, detail-oriented Senior Medical Writer with extensive experience contributing to nonclinical, clinical, and regulatory affairs teams in a dynamic industry setting. You will be responsible for delivering high-impact regulatory documents that advance our programs and support our mission to bring new the…

Gestionnaire principal(e), Affaires réglementaires CMC

On-site · Vancouver

Nous avons tous quelqu’un dans notre vie qui aura un jour besoin de médicaments. C’est pourquoi notre ambition est de toujours surmonter les obstacles pour mettre des médicaments novateurs à la disposition des patientes et des patients qui en ont besoin. Nous sommes en quête de vérité et de rigueur scientifique, et avons le courage d’explorer les frontières de l’inconnu. Nous sommes à la recherche d’une personne gestionnaire principale en affaires réglementaires (AR) CMC qui travaillera en étroite collaboration avec les équipes de la Fabrication et de la Qualité pour mettre en œuvre et docum…

Director, CMC Quality

On-site · Vancouver

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. We are looking for an experienced Director, CMC Quality to serve as a technical quality expert for antibody products during clinical development all the way through post-commercialization. As a core member of the CMC team, you will provide quality leadership and serve as the single point of contact representing all quality functio…

Analyste de systèmes cliniques

On-site · Montréal

Nous avons tous quelqu’un dans notre vie qui aura un jour besoin de médicaments. C’est pourquoi notre ambition est de toujours surmonter les obstacles pour mettre des médicaments novateurs à la disposition des patientes et des patients qui en ont besoin. Nous sommes en quête de vérité et de rigueur scientifique, et avons le courage d’explorer les frontières de l’inconnu. Nous sommes à la recherche d’une personne motivée pour se joindre à notre équipe des Opérations d’affaires à titre d’analyste de systèmes cliniques. Vous offrirez du soutien sur le terrain pour la mise en place et le maintie…

Scientist II/Senior Scientist

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.

External QA Specialist/Manager

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.

QA Specialist - Supplier Quality

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.

QC Analyst II

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.

Senior QC Data Reviewer

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.

Senior Manager, QC Microbiology

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.

QA for QC Specialist (15-month contract)

On-site · Vancouver

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. 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 state-of…

QA Specialist - Batch Record Review

On-site · Vancouver

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. 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 batches made in…

QA Operations Specialist (15-month contract)

On-site · Vancouver

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. 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 documenta…

VP, Medical Affairs

On-site · Vancouver

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. 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 developing pat…

Director, DP MSAT

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.

Associate Research Scientist - In Vivo Science

On-site · Vancouver

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. 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 analytical phases…

Research Scientist II - In Vivo Science

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.

VP, Medical Affairs

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.