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’un coordonnateur ou d’une coordonnatrice de recherche clinique (CRC) pour notre équipe des activités cliniques de Montréal (Québec). Pour occuper ce poste, vous devez être bilingue, avoir une capacité d’organisation pointue et le souci du détail. Dans le cadre de vos fonctions, vous soutiendrez la gestion des essais cliniques à toutes les étapes, du lancement de l’essai à sa clôture, en vous assurant que toutes les activités liées à l’essai sont exécutées conformément aux exigences réglementaires, aux bonnes pratiques cliniques (BPC) et aux politiques de l’entreprise. Vous devrez principalement participer aux tâches inhérentes à la réalisation d’un essai clinique, à savoir le maintien des documents de l’essai, la coordination des réunions, le soutien logistique et les communications liées à l’essai.

Ce que vous pourriez être appelé(e) à faire :

• Participer à la préparation et à la soumission de documents réglementaires et du matériel d’essai clinique;
• Veiller à ce que les documents essentiels et réglementaires de l’essai soient exacts et à jour;
• Coordonner et planifier les réunions, effectuer les activités préparatoires et générer les procès-verbaux;
• Soutenir l’équipe clinique en assurant le suivi et en rédigeant des rapports sur les étapes du projet, l’échéancier et les produits livrables;
• Participer à la préparation et à la distribution des communications en lien avec les essais cliniques aux centres cliniques et aux fournisseurs;
• Fournir un soutien administratif à l’équipe clinique et aux autres membres s’il a lieu;
• Collaborer avec l’équipe en remplissant et en révisant les documents d’activation des centres et les listes de vérification afin d’en assurer l’exactitude avant l’envoi des médicaments;
• Vérifier et faire le suivi des activités de paiements et des tâches liées aux comités d’éthique, aux centres de recherche et aux fournisseurs;
• Aider à la mise en place des ententes de confidentialité (Confidential Disclosure Agreement/CDA), des contrats des centres cliniques et des budgets. 

Nous aimerions avoir de vos nouvelles si :

• Vous possédez au moins 2 ans d’expérience dans un contexte de recherche clinique dans un poste similaire comprenant la coordination d’activités de recherche clinique.
• Vous avez acquis des connaissances pratiques sur les BPC de la CIH et sur les bonnes pratiques de documentation.
• Communicateur ou communicatrice d’exception, vous êtes bilingue et vous excellez dans les relations interpersonnelles et interfonctionnelles.
• Vous êtes proactif(e) dans la résolution de problèmes et capable de générer des solutions de façon autonome.
• Vous êtes en mesure d’établir des priorités et vous excellez dans un environnement au rythme soutenu.
• Vous avez un sens aigu des responsabilités et vous faites preuve d’une grande rigueur.

Ce que nous offrons :

En plus de votre salaire de base, nous offrons des actions, une prime annuelle selon le rendement de l’équipe et de l’entreprise, de même qu’une cotisation de 6 % à un REER (sans cotisations complémentaires).

Vous disposerez également d’une allocation annuelle de 1500 $ CA pour un mode de vie actif, de vacances annuelles, de la possibilité d’horaires flexibles, d’occasions de perfectionnement professionnel et d’un régime de soins de santé complet. Le mentorat scientifique et technique est également l’une de nos priorités. Grâce à nos initiatives, nos clubs et nos activités sociales, vous découvrirez également le fort esprit de communauté et les liens étroits qui unissent les membres d’AbCellera.

L’organisation : 

La mise au point de médicaments est la tâche la plus importante qui soit.

AbCellera est une entreprise de biotechnologie en phase clinique, spécialisée dans la découverte et le développement de médicaments à base d’anticorps dans les domaines de l’endocrinologie, de la santé des femmes, de l’immunologie et de l’oncologie. Nous avons mis en place une plateforme permettant de faire progresser les programmes de développement de médicaments à base d’anticorps, de la cible à la phase clinique, et nous l’utilisons pour élargir notre gamme de produits internes.

À l’heure actuelle, notre gamme comprend deux candidats-médicaments en phase de développement clinique, deux candidats en phase préclinique (DC) faisant l’objet d’activités préparatoires à la demande d’autorisation de nouveau médicament expérimental, ainsi que plus de 20 programmes de recherche actifs couvrant diverses modalités thérapeutiques et indications.

Nous avons la conviction que les personnes déterminées peuvent véritablement avoir un effet positif si elles partagent une vision commune et travaillent ensemble. C’est pourquoi la personnalité et l’intelligence sont au cœur de notre processus de recrutement, au-delà du CV ou de l’expérience.

Nous recherchons des personnes dynamiques et énergiques en qui nous pouvons avoir confiance. Elles doivent avoir besoin de sentir que leurs journées sont employées à bon escient et que leur travail compte vraiment. Au final, notre succès se définit par les bienfaits que nos médicaments apportent aux patients.

Pour postuler :

Soumettez votre candidature via notre site Web et mentionnez le numéro de poste 23358 dans votre lettre de motivation. Comme nous recevons un grand nombre de candidatures, nous ne contacterons que les personnes sélectionnées pour une entrevue. Toutes les communications de notre équipe de découverte de talents proviendront d’une adresse de courriel @abcellera.com.

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 Compliance/Validation Engineer to join the Engineering Asset Management team and support execution of CQV (Commissioning, Qualification, Validation) and engineering compliance activities, in alignment with regulatory expectations and Good Manufacturing Practices. This role is for you if you bring hands-on experience in a pharmaceutical or biotech environment, paired with sharp analytical thinking, a keen eye for detail, and the confidence to influence and align cross-functional teams.

How you might spend your days

• Authoring and reviewing CQV protocols, SOPs, and technical documentation, ensuring everything meets rigorous GMP standards and holds up under scrutiny
• Leading investigations into deviations and non-conformances, driving CAPA implementation that gets to the root cause and keeps issues from coming back
• Being a trusted voice for the engineering team during internal and external audits 
• Coordinating and executing engineering and quality change controls, keeping projects moving without compromising compliance
• Drafting and executing CQV deliverables, from User Requirement Specifications to protocols, summary reports, and periodic reviews, on an electronic VLMS
• Managing the full lifecycle of engineering drawings and documents through e-systems, bringing structure and precision to everything you touch
• Performing periodic reviews of all qualified systems at our GMP manufacturing facility to ensure ongoing compliance and performance
• Shaping how the team measures success by supporting the development and tracking of departmental KPIs

We'd love to hear from you if

• You hold a Bachelor's degree in Engineering, Chemistry, or a related life science field, and you've spent 3+ years putting that knowledge to work in a similar role
• You're comfortable navigating electronic VLMS and QMS platforms, and know how to get the most out of them in a fast-paced GMP environment
• You're the person who catches what others miss; detail-oriented by nature, with documentation and organizational skills that others rely on
• You bring a proactive, can-do attitude to problem-solving; when an issue arises, you're already thinking about the solution
• You thrive in a collaborative team setting and know how to communicate clearly across functions
• You are familiar with AutoCAD or Revit (this is a bonus!)
• You're a natural at juggling competing priorities; managing multiple tasks without letting anything slip through the cracks

What we offer

AbCellera’s hiring range for this role is CAD $73,000 - $87,000 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. 

You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera

Creating medicines is the most important work we can do. 

We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply

Please submit your application through our website and refer to Job ID 23367 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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 an experienced, hands-on QC Microbiology Lead - someone who wants to own a program end-to-end - from hands-on testing and troubleshooting to guiding the team around you. This is a primarily bench-based role; you will be in the lab daily, running and troubleshooting assays alongside your team rather than managing from a distance. You will bring deep technical expertise and a strong in-lab presence across microbial methods, EM programs, utilities monitoring, and contamination investigations, while also supporting broader QC functions such as stability, sample management, raw materials testing, and analytical assays including UPLC, ELISA, or spectrophotometry.

How you might spend your days

• Providing daily in-lab mentorship to the QC team, fostering strong technique, aseptic practices, and microbiological best practices
• Leading all Microbiology operations, including bioburden, endotoxin, microbial ID, growth promotion, EM sampling, water testing, and trending
• Troubleshooting microbiological assays, contamination events, and EM deviations, ensuring timely and compliant resolution
• Ensuring microbiology labs and adjacent QC spaces remain inspection-ready, including GMP housekeeping and equipment readiness
• Coordinating stability pulls, sample preparation, testing, and data tracking across QC programs
• Overseeing sample receipt, chain-of-custody, aliquoting, storage conditions, and distribution workflows
• Supporting routine sampling, testing, and trending of Utilities (WFI, clean steam, compressed gases) with appropriate documentation
• Reviewing micro data packages, protocols, reports, and testing documentation for accuracy and adherence to ALCOA++ principles
• Collaborating with Analytical Development, Quality Assurance, Materials, and Manufacturing teammates to ensure smooth operational flow and timely release/testing

We'd love to hear from you if

• You bring deep, hands-on microbiology experience in a regulated (GMP) QC environment, and are confident in leading microbial methods, EM programs, utilities monitoring, and contamination troubleshooting
• You have experience mentoring or leading team members working within microbiology labs or cleanroom/controlled environments
• You have 8+ years of hands-on QC microbiology experience in a GMP setting, in addition to a Bachelor’s degree in Microbiology or a related life sciences field
• You communicate clearly, collaborate well, and maintain calm, structured decision-making under pressure
• You demonstrate strong ownership, accountability, and a solutions-focused mindset when supporting analysts or resolving micro-related issues
• You are organized, detail-oriented, and committed to inspection readiness and data integrity
• You thrive in an environment requiring in-lab leadership, cross-functional coordination, and prioritization of operational needs
• You have experience with stability programs, sample management workflows, and raw materials testing coordination
• You are familiar with analytical assays such as UPLC, ELISA, or spectrophotometry (desirable)

What we offer

AbCellera’s hiring range for this role is CAD $105,600 - $132,000 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. 

You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera

Creating medicines is the most important work we can do.

We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply

Please submit your application through our website and refer to Job ID 23334 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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 QA Operations Manager to serve as a trusted Quality partner on the cleanroom floor, providing real-time GMP oversight for our Drug Substance manufacturing operations. In this role, you will lead the development and implementation of quality systems and procedures, drive end-to-end management of quality events including deviations, CAPAs, and change controls, and play a key role in supporting clinical batch disposition. You will partner closely with cross-functional teams across Manufacturing, Supply Chain, Quality Control and Facilities & Engineering to ensure inspection readiness and regulatory compliance as we advance our antibody therapy pipeline. This is a unique opportunity to help shape quality operations at a pivotal stage of AbCellera's growth.

How you might spend your days

• Developing and implementing quality systems and oversight programs for Drug Substance (DS) GMP manufacturing, including product changeovers, batch record review, and shop floor surveillance
• Partnering with CMC teams as the embedded QA representative, contributing quality expertise and guidance to ensure regulatory and quality requirements are seamlessly integrated across CMC projects
• Completing review and approval of GMP documentation - such as batch records, SOPs, logbooks, risk assessments - ensuring full GMP and regulatory alignment and in support of clinical batch disposition
• Maintaining inspection readiness of the facility and identifying and escalating risks to members of the site leadership team 
• Supporting inspections and audits of the clinical manufacturing facility
• Participating in end-to-end quality event management, including deviations, investigations, CAPAs, and change controls, collaborating cross-functionally to drive root cause analysis and on-time record closure
• Contributing to manufacturing risk assessments, from identification and evaluation through to mitigation, documentation, and reporting
• Managing material qualification reviews to support procurement and GMP compliant use of raw materials and components
• Acting as a key quality partner across Manufacturing, QC, Supply Chain, F&E, and project management teams, ensuring seamless quality oversight of DS programs
• Staying ahead of evolving Quality and Regulatory requirements, proactively assessing their impact on AbCellera and driving timely mitigation strategies to maintain compliance
• Supporting broader Quality Assurance activities, as required by program deliverables, such as QA for QC, QA for materials management, and opportunities identified by the Quality team

We'd love to hear from you if

• You hold a Bachelor's or Master's degree in a relevant scientific discipline and bring 8+ years of GxP industry experience, with at least 5 years in a quality management or leadership role within pharmaceuticals, biotechnology, or a comparable regulated environment
• You have a strong command of current pharmaceutical regulations and guidances including FDA, Health Canada, EU, and ICH, and understand how they apply in practice
• You bring hands-on experience with biological Drug Substance and aseptic manufacturing processes, including associated testing requirements
• You're comfortable navigating systems such as ERP (SAP), eQMS, and LIMS, and can hit the ground running in a tech-enabled manufacturing environment
• You communicate with clarity and confidence, equally effective presenting to both technical and non-technical stakeholders
• You're a self-starter who takes ownership, drives results, and thrives with autonomy in a fast-moving, mission-driven environment

What we offer

AbCellera’s hiring range for this role is CAD $105,000 - $120,000 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. 

You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera

Creating medicines is the most important work we can do. 

We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply

Please submit your application through our website and refer to Job ID 23366 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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 an experienced, strategically minded Principal Scientist to join our expanding Non-Clinical Safety team based in Vancouver, Canada. You will be responsible for designing, planning, monitoring, and reporting of non-GLP and GLP toxicology studies and provide nonclinical safety support for early to late stage programs. 

How you might spend your days

• Leading the planning, design, execution and interpretation of nonclinical toxicology programs in support of IND, CTA and BLA submissions, including general toxicity and reproductive and developmental toxicology studies, in alignment with global regulatory expectations and program strategy
• Serving as the primary scientific interface with contract research organizations (CROs), providing strategic oversight during protocol development, study conduct, data interpretation, and report finalization to ensure timely, high-quality, and GLP-compliant delivery of nonclinical studies
• Representing the Nonclinical Safety function as a core member of cross-functional discovery and development program teams, contributing toxicology expertise to inform candidate selection, risk assessment, and overall program advancement
• Providing critical scientific assessment of toxicology data and communicating clear, actionable risk-benefit evaluations and recommendations to project teams and senior leadership, including potential implications for clinical development and regulatory strategy 
• Authoring and reviewing nonclinical safety sections of regulatory documents (INDs, CTAs, IBs, and BLAs), and contributing as a subject matter expert to global regulatory interactions and health authority responses
• Driving the development and evolution of integrated nonclinical safety strategies across AbCellera’s therapeutic portfolio, ensuring consistency, scientific rigor, and alignment with company objectives
• Maintaining scientific leadership by staying current with advances in toxicology science, methodologies, and evolving regulatory guidance, and proactively translating these insights into best practices for internal programs

We'd love to hear from you if

• You bring deep expertise in GLP-compliant nonclinical toxicology, including hands-on experience with US FDA 21 CFR Part 58, and a strong working knowledge of FDA, ICH, and EMA nonclinical regulatory guidance
• You have a proven track record of designing, overseeing, and interpreting non-GLP and GLP toxicology studies in support of discovery and development programs; experience with oncology and/or ADC programs is highly desirable
• You hold a PhD in Toxicology or a related field, with 8+ years of relevant industry experience supporting biologics development; candidates with a MSc degree and 12+ years of directly applicable experience will also be considered
• You demonstrate the ability to lead scientific discussions and influence decision-making within highly matrixed, cross-functional teams through clear, confident, and effective communication
• You possess excellent scientific writing skills, with experience authoring and reviewing toxicology reports and regulatory submission documents
• You exhibit strong organizational and prioritization skills, enabling effective management of multiple programs and timelines in a fast-paced environment
• You apply sound scientific judgment and critical problem-solving skills to assess complex datasets, identify risks, and propose strategic solutions
• You thrive in a dynamic, evolving environment, demonstrating flexibility, resilience, and a proactive approach to change
• You hold DABT accreditation (highly desirable, but not required)

What we offer

AbCellera’s hiring range for this role is CAD $134,000 - $168,000 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. 

You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera

Creating medicines is the most important work we can do. 

We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply

Please submit your application through our website and refer to Job ID 23346 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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.

As the Specialist, QC Systems, you will support the design, implementation, and ongoing management of the Quality Management System (QMS) for QC-related CMC/GMP activities. Your role will play a critical part in ensuring the effective implementation, execution, and continuous improvement of the QMS framework within AbCellera, while maintaining compliance with applicable global regulations and regulatory expectations.

You will ensure that the QC laboratory electronic systems (eSystems) are fit-for-purpose, compliant, and enable efficient, data-driven laboratory operations. Working cross-functionally, you will help foster a strong culture of quality across the CMC/GMP organization. You will be empowered with a high degree of ownership and autonomy to innovate, move quickly, and build scalable quality and digital capabilities that leave a lasting impact on our organization and industry.

How you might spend your days

• Supporting, maintaining, monitoring, and continuously improving the QC Quality Management System (QMS) framework and associated quality system processes in compliance with applicable global CMC/GMP requirements
• Supporting the operation, administration, and lifecycle management of QC laboratory electronic systems (eSystems), ensuring they effectively support sample management, analysis, data acquisition, data review, and result reporting in compliance with global GMP, data integrity, and regulatory requirements
• Contributing to the design, implementation, and evolution of the QC data architecture, identifying eSystem capabilities needed to support QC workflows, data integrity (ALCOA++), and phase-appropriate compliance
• Supporting the Business Process Owner (BPO) for QC laboratory systems (e.g. LIMS, LES, CDS), overseeing system changes, enhancements, and upgrades throughout the system lifecycle
• Overseeing and maintaining QC eSystems master data, including user roles, permissions, system configurations, and controlled data objects
• Developing, reviewing, and maintaining GMP procedures, work instructions, controlled documentation, and training materials governing the compliant and effective use, administration, and data management of QC eSystems, including delivery of end-user training sessions
• Providing QC eSystem support for investigations, deviations, and CAPAs, including data retrieval, audit trail review, and system impact assessments
• Supporting qualification and computer system validation activities for QC systems (e.g., protocol and risk assessment review, validation deviations/exceptions, and lifecycle documentation)
• Supporting QC eSystem licensing, user access, vendor relationships, and budgeting/forecasting for QC digital infrastructure
• Collaborating cross-functionally with QC, Quality Systems, IT, Engineering, Validation, and external vendors to ensure QC eSystems are fit-for-purpose, compliant, and aligned with laboratory and business processes

We’d love to hear from you if

• You have 3+ years of experience managing quality systems in a GxP-regulated environment, with demonstrated application of global CMC/GMP requirements and relevant regulations and guidance
• You have a Bachelor’s degree in a relevant scientific or engineering discipline with 5+ years of industry experience in biotechnology, pharmaceuticals, or life sciences
• You have strong understanding and hands-on experience with quality management systems and continuous improvement principles, including their application to QC laboratory operations and regulated environments
• You have a solid understanding of drug development processes from discovery through CMC development, with the ability to translate business and regulatory requirements into practical, compliant solutions
• You have experience supporting, configuring, or owning QC laboratory electronic systems (e.g., LIMS, LES, CDS) in a GMP-regulated environment, including system lifecycle management and change control
• You are proactive in identifying opportunities for improvement, with strong critical thinking and problem-solving skills

What we offer

AbCellera’s hiring range for this role is CAD $76,000 - $95,000 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. 

You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera

Creating medicines is the most important work we can do. 

We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply

Please submit your application through our website and refer to Job ID 23342-D in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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.

As the Manager, QC Systems, you will support the design, implementation, and ongoing management of the data architecture and eSystems required to support QC-related CMC/GMP activities. Your role will play a critical part in ensuring the effective implementation, execution and continuous improvement of the QC-related eSystems within AbCellera, while maintaining compliance with applicable global regulations and regulatory expectations.

You will provide functional ownership and oversight of QC laboratory electronic systems (eSystems), ensuring they are fit-for-purpose, compliant, and enable efficient, data-driven laboratory operations. Working cross-functionally, you will help foster a strong culture of quality across the CMC/GMP organization. You will be empowered with a high degree of ownership and autonomy to innovate, move quickly, and build scalable quality and digital capabilities that leave a lasting impact on our organization and industry.

How you might spend your days

• Establishing, supporting, maintaining, monitoring, and continuously improving the QC Quality Management System (QMS) framework and associated quality system processes in compliance with applicable global CMC/GMP requirements
• Supporting the operation, administration, and lifecycle management of QC laboratory electronic systems (eSystems), ensuring they effectively support sample management, analysis, data acquisition, data review, and result reporting in compliance with global GMP, data integrity, and regulatory requirements
• Contributing to the design, implementation, and evolution of the QC data architecture, identifying eSystem capabilities needed to support QC workflows, data integrity (ALCOA++), and phase-appropriate compliance
• Serving as the Business Process Owner (BPO) for QC laboratory systems (e.g. LIMS, LES, CDS), overseeing system changes, enhancements, and upgrades throughout the system lifecycle
• Overseeing and maintaining QC eSystems master data, including user roles, permissions, system configurations, and controlled data objects
• Developing, reviewing, and maintaining GMP procedures, work instructions, controlled documentation, and training materials governing the compliant and effective use, administration, and data management of QC eSystems, including delivery of end-user training sessions
• Providing QC eSystem support for investigations, deviations, and CAPAs, including data retrieval, audit trail review, and system impact assessments
• Supporting qualification and computer system validation activities for QC systems (e.g., protocol and risk assessment review, validation deviations/exceptions, and lifecycle documentation)
• Managing QC eSystem licensing, user access, vendor relationships, and budgeting/forecasting for QC digital infrastructure
• Collaborating cross-functionally with QC, Quality Systems, IT, Engineering, Validation, and external vendors to ensure QC eSystems are fit-for-purpose, compliant, and aligned with laboratory and business processes

We’d love to hear from you if

• You have 5+ years of experience managing quality systems in a GxP-regulated environment, with demonstrated application of global CMC/GMP requirements and relevant regulations and guidance
• You have a Bachelor’s degree in a relevant scientific or engineering discipline with 8+ years of industry experience in biotechnology, pharmaceuticals, or life sciences
• You have strong understanding and hands-on experience with quality management systems and continuous improvement principles, including their application to QC laboratory operations and regulated environments
• You have a solid understanding of drug development processes from discovery through CMC development, with the ability to translate business and regulatory requirements into practical, compliant solutions
• You have experience supporting, configuring, or owning QC laboratory electronic systems (e.g., LIMS, LES, CDS) in a GMP-regulated environment, including system lifecycle management and change control
• You are proactive in identifying opportunities for improvement, with strong critical thinking and problem-solving skills

What we offer

AbCellera’s hiring range for this role is CAD $94,880 - $118,600 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. 

You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera

Creating medicines is the most important work we can do. 

We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply

Please submit your application through our website and refer to Job ID 23342 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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 a motivated and meticulous individual, with extensive experience conducting in vivo studies in accordance with Animal Use Protocols and Standard Operating Procedures, to join our team. You will contribute to the discovery of therapeutic antibodies and subsequent efficacy assessments, and through teamwork, innovation, and mutual support, together we will tackle the most challenging scientific problems.

How you might spend your days: 

• Overseeing day-of-study activities; supporting efficient and high-quality study execution
• Collaborating with study leads, scientists, and cross-functional teammates, ensuring alignment on study protocols, animal welfare considerations, and animal macro- and micro-environment requirements of in vivo studies
• Providing technical support, troubleshooting, and problem-solving solutions, while identifying opportunities for process improvement and implementing best practices to optimize workflow efficiency
• Contributing to the preparation of Animal Use Protocols (AUPs) and Standard Operating Procedures (SOPs) to comply with CCAC Regulations and Guidelines
• Ensuring accurate recording of in vivo data across all studies, and supporting teammates with data analysis as required
• Training and mentoring team members to ensure compliance with safety policies, SOPs, and regulatory requirements
• Performing in vivo and ex vivo techniques to support study objectives, applying deep technical expertise in in vivo procedures
• Carrying out daily health assessments and clinical observations, ensuring high standards of animal welfare and accurate documentation
• Preparing and maintaining laboratory spaces, equipment, and consumables required for in vivo and ex vivo work
• Preparing and aliquoting reagents required for in vivo studies

We'd love to hear from you if:

• You provide the highest level of animal care while overseeing and performing in vivo activities
• You are experienced with animal handling, dosing (IV, IP, SQ), and blood collection, and have a strong understanding of the 3Rs and research ethics
• You have 6+ years of experience in an in vivo research environment; a BSc, MSc, and/or experience with in vitro and ex vivo techniques are considered assets
• Managing competing priorities comes with ease for you, and you thrive in a collaborative, fast-paced work environment
• You take pride in being a self-motivated person, fast learner, team player, and creative problem solver
• You have excellent communication, documentation, and organizational skills, and are known for your accountability and reliability
• You are able to lift up to 25 kg, and are comfortable with long periods of standing and bending throughout your day
• You are able to work at least one weekend day per week

What we offer:

AbCellera’s hiring range for this role is CAD $75,800 - $94,700 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. 

You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, opportunity for flexible work arrangements, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera:

Creating medicines is the most important work we can do. 

We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline. 

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply:

Please submit your application through our website and refer to Job ID 23365 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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 a motivated and meticulous individual, with extensive experience conducting in vivo studies in accordance with Animal Use Protocols and Standard Operating Procedures, to join our team on either a Tuesday to Saturday or Sunday to Thursday work schedule. You will contribute to the discovery of therapeutic antibodies and subsequent efficacy assessments, and through teamwork, innovation, and mutual support, together we will tackle the most challenging scientific problems. 

How you might spend your days: 

• Performing in vivo and ex vivo techniques to support study objectives, applying deep technical expertise in in vivo procedures
• Carrying out daily health assessments and clinical observations, ensuring high standards of animal welfare and accurate documentation
• Contributing hands-on expertise during day-of-study activities, supporting efficient and high-quality study execution
• Preparing and maintaining laboratory spaces, equipment, and consumables required for in vivo and ex vivo work
• Troubleshooting technical challenges in real time, identifying opportunities to improve procedures and workflow efficiency
• Ensuring accurate and complete recording of in vivo study data, maintaining strong documentation and data integrity practices
• Sharing technical knowledge and best practices with team members, supporting strong adherence to SOPs, safety standards, and regulatory requirements
• Working closely with study managers and research teams to ensure alignment with study protocols and animal welfare consideration

We'd love to hear from you if:

• You provide the highest level of animal care while overseeing and performing in vivo activities
• You have strong expertise in  animal handling, dosing (IV, IP, SQ), and blood collection, and have a strong understanding of the 3Rs and research ethics
• You have 6+ years of experience in an in vivo research environment; a BSc, MSc and experience with in vitro, in vivo, and ex vivo techniques for PK and oncology models are considered assets
• Managing competing priorities comes with ease for you, and you thrive in a collaborative, fast-paced work environment
• You take pride in being a self-motivated person, fast learner, team player, and creative problem solver
• You have excellent communication, documentation, and organizational skills, and are known for your accountability and reliability
• You are able to lift up to 25 kg, and are comfortable with long periods of standing and bending throughout your day
• You are able to work at least one weekend day per week

What we offer:

AbCellera’s hiring range for this role is CAD $75,800 - $94,700 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. 

You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, opportunity for flexible work arrangements, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera:

Creating medicines is the most important work we can do. 

We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline. 

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply:

Please submit your application through our website and refer to Job ID 23353 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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 a motivated and meticulous individual, with extensive experience conducting in vivo studies in accordance with Animal Use Protocols and Standard Operating Procedures, to join our team on either a Tuesday to Saturday or Sunday to Thursday work schedule. You will contribute to the discovery of therapeutic antibodies and subsequent efficacy assessments, collaborating with teammates through innovation, mutual support, and shared expertise. If you love contributing directly to in vivo research through hands-on lab work, this is the role for you! 

How you might spend your days: 

• Performing in vivo and ex vivo techniques to support in vivo studies 
• Carrying out daily health assessments and recording clinical observations
• Supporting in vivo day-of-study operations to ensure smooth execution and to maximize efficiency
• Organizing and preparing lab spaces, materials/consumables, and equipment for in vivo and ex vivo activities
• Providing technical support and problem-solving solutions, while identifying opportunities for process improvement and implementing best practices to optimize workflow efficiency 
• Ensuring accurate recording of in vivo data across all studies and supporting teammates with data entry as required
• Training and mentoring team members to ensure compliance with safety policies, SOPs, and regulatory requirements
• Collaborating with study managers, ensuring alignment on study protocols and animal welfare considerations

We'd love to hear from you if:

• You provide the highest level of animal care while overseeing and performing in vivo activities
• You are experienced with animal handling, dosing (IV, IP, SQ), and blood collection, and have a strong understanding of the 3Rs and research ethics
• You have 4+ years of experience in an in vivo research environment; a BSc, and experience with in vitro, in vivo, and ex vivo techniques for PK and oncology models are considered assets
• You manage competing priorities seamlessly and you thrive in a collaborative, fast-paced lab environment
• You take pride in being a self-motivated person, fast learner, team player, and creative problem solver
• You have excellent communication, documentation, and organizational skills, and are known for your accountability and reliability
• You are able to lift up to 25 kg, and are comfortable with long periods of standing and bending throughout your day
• You are able to work at least one weekend day per week

What we offer:

AbCellera’s hiring range for this role is CAD $58,800 - $74,000 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. 

You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, opportunity for flexible work arrangements, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera:

Creating medicines is the most important work we can do. 

We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline. 

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply:

Please submit your application through our website and refer to Job ID 23353 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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 a highly organized, and detail-oriented Clinical Trial Coordinator (CTC) to join our Clinical Operations team. In this role, you will support the management of clinical trials from initiation to close-out, ensuring all trial-related activities are executed in compliance with regulatory requirements, Good Clinical Practice (GCP), and Company policies. Your role will be focused on supporting trial execution tasks, including maintaining trial documentation, coordinating meetings, handling logistics, and assisting with trial-related communications.

How you might spend your days

• Assisting with the preparation and submission of regulatory documents and clinical trial materials
• Maintaining accurate and up-to-date trial documentation, including study files, regulatory binders, and essential records
• Coordinating and scheduling meetings, preparation activities, and generating meeting minutes
• Supporting the clinical team with tracking and reporting on project milestones, timelines, and deliverables
• Assisting with the preparation and distribution of trial-related communications to clinical sites and vendors
• Providing administrative support for the clinical team and other members as needed
• Collaborating with colleagues to complete and review site activation documents and checklists for accuracy prior to drug shipment
• Reviewing and tracking payment activities and tasks related to ECs/IRBs, investigational sites, and vendors
• Assisting with the customization of CDAs, clinical site contracts, and budgets when applicable
• Acting as the Primary Owner of the eTMF "Health Check", ensuring documents provided by CRAs are filed correctly and in real-time

We'd love to hear from you if

• You have at least 2 years of demonstrated work experience in a clinical research environment, in a similar role involving coordination of clinical trial activities
• You have hands-on knowledge of ICH-GCP and Good Documentation Practices
• You are an outstanding cross-functional communicator and relationship builder
• You are a proactive problem-solver, able to generate solutions independently
• You have the ability to prioritize and thrive in a fast-paced environment
• You operate with a high sense of accountability and accuracy

What we offer

AbCellera’s hiring range for this role is CAD $61,000 - $72,000 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. 

You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera

Creating medicines is the most important work we can do. 

We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply

Please submit your application through our website and refer to Job ID 23358 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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 Warehouse Operator to join the materials management team at AbCellera. In this capacity, you will be a key member of the warehouse team responsible for ensuring the overall success of warehouse operations, including receiving, inspection, inventory control, storage, replenishment, packing, staging, shipping, and maintaining a safe and lean work environment. You will also work closely with your peers in Quality, Manufacturing, and Logistics to ensure efficient warehouse operations, and seamless information flow through SAP. 

How you might spend your days

• Performing daily warehouse activities such as receiving, inspecting and storing materials, items, and products to ensure they are sorted, labeled, and stored properly and in compliance with AbCellera’s standards and policies 
• Loading and unloading shipments, ensuring proper documentation and handling 
• Handling order-picking, packing, and staging activities to ensure timely and accurate order fulfillment 
• Appropriately transporting  the shipment of goods, accurately preparing bills of lading, and ensuring proper packaging of goods 
• Safely operating equipment, such as forklifts, reach trucks, battery charging equipment, pallet wrappers, pallet changers, compactors, dock levelers, etc. 
• Utilizing several devices such as Radio frequency technology (RFID), scanners, and others to read barcodes and transfer product information, quantities and location information directly into our warehouse management system 
• Performing regular inventory counts, reconciling discrepancies, monitoring stock levels, and coordinating replenishment activities to avoid shortages 
• Processing production orders and delivering on time
• Identifying and implementing continuous improvement initiatives to enhance warehouse efficiency and reduce waste

We’d love to hear from you if

• You hold a high school diploma or equivalent and an associate degree in logistics, supply chain management, or a related field 
• You have proven experience in warehouse operations, preferably in a similar role 
• You have experience in a GMP/GDP environment 
• You have a strong understanding of inventory management, logistics, and warehouse processes 
• You have excellent communication and interpersonal skills and the ability to work independently and as part of a team
• You have experience in SAP or similar ERP systems 
• You are physically able to perform repetitive tasks for extended periods, including lifting and standing
• You are comfortable working in a warehouse environment, including exposure to varying temperatures (e.g., cold room from 2º to 8º C) 
• You are available to work shifts, including occasional evenings and weekends 
• You hold a Forklift certification or are able to obtain one 

What we offer

AbCellera’s hiring range for this role is CAD $54,500 - $68,000 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. 

You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera

Creating medicines is the most important work we can do. 

We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply

Please submit your application through our website and refer to Job ID 23357 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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 skilled, hands-on Senior QC Microbiology Analyst to provide deep technical mentorship in the day-to-day QC laboratory operations, with a primary focus on Microbiology. You will provide a strong in-lab presence and lead troubleshooting expertise across microbial methods, EM programs, utilities monitoring, and contamination investigations.

How you might spend your days

• Leading Microbiology operations, including bioburden, endotoxin, microbial ID, growth promotion, EM sampling, water testing, and trending
• Troubleshooting microbiological assays, contamination events, and EM deviations, ensuring timely and compliant resolution
• Providing daily in-lab mentorship to the QC team, fostering strong technique, aseptic practices, and microbiological best practices
• Ensuring microbiology labs and adjacent QC spaces remain inspection-ready, including GMP housekeeping and equipment readiness
• Coordinating stability pulls, sample preparation, testing, and data tracking across QC programs
• Overseeing sample receipt, chain-of-custody, aliquoting, storage conditions, and distribution workflows
• Supporting routine sampling, testing, and trending of Utilities (WFI, clean steam, compressed gases) with appropriate documentation
• Reviewing micro data packages, protocols, reports, and testing documentation for accuracy and adherence to ALCOA++ principles

We'd love to hear from you if

• You bring deep, hands-on Microbiology experience in a regulated (GMP) QC environment, and are confident in leading microbial methods, EM programs, utilities monitoring, and contamination troubleshooting
• You have experience mentoring or leading team members working within microbiology labs or cleanroom/controlled environments
• You have 8+ years of hands-on QC microbiology experience in a GMP setting, in addition to a Bachelor’s degree in Microbiology or a related life sciences field
• You communicate clearly, collaborate well, and maintain calm, structured decision-making under pressure
• You demonstrate strong ownership, accountability, and a solutions-focused mindset when supporting analysts or resolving micro-related issues
• You are organized, detail-oriented, and committed to inspection readiness and data integrity
• You thrive in an environment requiring in-lab leadership, cross-functional coordination, and prioritization of operational needs

What we offer

AbCellera’s hiring range for this role is CAD $88,000 to $110,000 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. 

You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera

Creating medicines is the most important work we can do.

We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply

Please submit your application through our website and refer to Job ID 23334 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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 a Clinical Demand and Supply Manager who will be responsible for the end-to-end management of Investigational Medicinal Product (IMP) and ancillary supplies for global clinical trials. In this role, you are responsible for ensuring the right product is in the right place, at the right time, and in the right condition for our clinical studies and patients. You are a strong collaborator and will work extensively with cross-functional teams, including Clinical Operations, CMC, Quality Assurance and Regulatory Affairs, as well as manage external partners (CMOs, depots and couriers) to execute flawless clinical supply strategies. 

How you might spend your days

• Developing and maintaining global supply plans for clinical trials, including demand planning forecasts across AbCellera’s programs
• Managing and maintaining global inventory across all central depots and clinical sites, ensuring uninterrupted supply while utilizing ERP/inventory systems for accurate record keeping
• Managing packaging, labelling, and distribution activities with CMO partners
• Coordinating global shipments of clinical supplies, ensuring strict compliance with international trade regulations, import/export requirements, and customs documentation
• Managing and qualifying temperature-controlled shipments (cold chain), collaborating  with Quality Assurance to resolve any temperature excursions
• Collaborating with teams and vendors to set up, manage and lead  User Acceptance Testing (UAT) for Interactive Response Technology (IRT/IXRS) systems governing inventory, randomization, and drug assignment
• Ensuring all clinical supply activities strictly adhere to Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), and global regulations
• Acting as the Clinical Supply Subject Matter Expert on clinical study teams, collaborating with CMC, Regulatory Affairs (label approvals/submission requirements), and Clinical Operations
• Overseeing drug accountability, returns, and destruction, ensuring complete documentation, and assisting in the developing and managing of the clinical supply budget for assigned studies

We'd love to hear from you if

• You have demonstrated expertise in cGMP, GCP, and global clinical trial regulations (e.g., FDA, EMA) as well as experience managing packaging, labeling, and distribution partners (CMOs and all external partner organizations)
• You have a Bachelor’s degree in a scientific discipline, Supply Chain Management, or a related field, plus 8+ years of relevant work experience in the pharmaceutical or biotechnology industry, with at least 3 years in a direct clinical supply chain role
• You have hands-on experience with Interactive Response Technology (IRT/IXRS) systems is essential
• You have proven ability to manage complex, temperature-controlled (cold chain) logistics

What we offer

AbCellera’s hiring range for this role is CAD $124,560 - $155,700 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. 

You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

Our headquarters is in Vancouver and working on site is highly desirable. For this position, remote applications will be considered. 

About AbCellera

Creating medicines is the most important work we can do. 

We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply

Please submit your application through our website and refer to Job ID 23337 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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 a Medical Director to join our Clinical Development team, to provide medical and scientific leadership for our pipeline programs in the areas of endocrinology and autoimmune diseases from pre-IND/CTA stage through Phase 1/FIH and later stage trials. You will lead the cross-functional program team and drive the development strategy, including study design, execution, interpretation, and reporting of clinical trials, ensuring the highest standards of safety and regulatory compliance.

How you might spend your days

• Leading the medical strategy for assigned clinical development programs in endocrinology and/or autoimmune diseases
• Designing and authoring clinical protocols (Phase 1-3), investigator brochures, clinical study reports (CSRs), and regulatory documents (IND, CTA)
• Serving as the Medical Monitor for assigned trials, overseeing patient eligibility, safety, and protocol adherence
• Interpreting clinical trial data, including safety, efficacy, and pharmacokinetics/pharmacodynamics (PK/PD), and translate findings into actionable development strategy
• Providing medical expertise for the ongoing assessment and management of patient safety, including reviewing cumulative safety data, serious adverse events (SAEs) and contributing to safety reports (DSURs)
• Ensuring all clinical development activities are conducted in accordance with Good Clinical Practice (GCP), relevant regulatory requirements, and company standard operating procedures (SOPs)
• Serving as the primary clinical contact for assigned programs to internal teams, external investigators, and regulatory agencies
• Establishing and maintaining collaborative relationship with medical experts and investigators in the assigned therapeutic areas of development
• Collaborating closely with cross-functional teams, including Translational Science, Clinical Operations, Regulatory Affairs, Biostatistics, and Corporate Development
• Developing publications, present data and strategy to governance committees and at external meetings

We’d love to hear from you if

• You have an M.D. (Doctor of Medicine) or equivalent degree; Board Certification or eligibility in Endocrinology, Rheumatology, or Internal Medicine is preferred
• You have 12+ years of clinical development and leadership experience in the pharmaceutical or biotechnology industry
• You have a proven track record in the design, execution, and analysis of Phase 1-2 clinical trials
• You have excellent communication, presentation, and interpersonal skills, and are capable of influencing strategy across all levels of the organization
• You have experience with biologic agents (such as monoclonal antibodies), and/or novel modalities (bispecifics, T-cell engagers, ADC)
• You have experience interacting with major regulatory agencies (FDA, Health Canada, EMA)
• You have experience with translational medicine and biomarker development in clinical trials

What we offer

AbCellera’s hiring range for this role is currently under review and will be commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. 

You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera

Creating medicines is the most important work we can do. 

We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply

Please submit your application through our website and refer to Job ID 23331 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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 an Associate Director, CMC Regulatory Affairs (RA) who will work closely with our manufacturing and quality teams to develop and implement global CMC strategies for multiple biologics programs, from pre-clinical through Phase 3 studies. You will be a key member of project teams, shaping the CMC RA strategy and documentation for innovative new biologics and ensuring submissions are aligned with health authority requirements and delivered on time with quality.

How you might spend your days:

• Serving as the primary CMC regulatory representative in project meetings and with regulatory agencies 
• Preparing CMC regulatory submissions including briefing documents, IND submissions, and CTA filings 
• Overseeing the preparation of responses to regulatory authority queries
• Managing critical CMC regulatory timelines, working with team members to navigate the pathways for manufacturing and analytical development, working in close partnership with the CMC and Quality teams 
• Staying on top of detailed knowledge of the global regulatory environment relevant for biologics, communicating changing regulatory agency requirements, and supporting pertinent regulatory intelligence per needs of programs
• Collaborating with external consultants, CDMOs, and CROs to provide regulatory guidance
• Evaluating regulatory CMC program risks and establishing mitigation strategies pertinent to product development
• Partnering with CMC, Discovery, and Clinical Development teams to innovate strategies to accelerate submission timelines 

We'd love to hear from you if:

• You have a deep understanding of CMC regulatory requirements, eCTD structure, and Module 3 preparation (BLAs/NDAs/NDSs) for biologics and combination products
• You can seamlessly navigate regulatory requirements for CMC submissions for biologics and combination products, and look forward to the preparation of regulatory submissions
• You have a thorough understanding of Health Canada, FDA, and EMA regulations 
• You can efficiently oversee independent contractors and vendors
• You are a skilled regulatory writer with effective oral communication skills
• You are a detailed oriented individual, highly organized, and thrive in fast paced environments while managing multiple priorities.
• You have a relevant post-secondary degree(s) in biological, pharmaceutical, chemical, engineering sciences or a related field, plus about 12 years of relevant work experience

What we offer:

AbCellera’s hiring range for this role is CAD $141,000 - $170,000 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. 

You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera:

Creating medicines is the most important work we can do. 

We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply:

Please submit your application through our website and refer to Job ID 23350 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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 a Medical Director to join our Clinical Development team, to drive clinical strategy for our oncology pipeline. You will provide medical and scientific leadership for early oncology programs from pre-IND/CTA stage through Phase 1-2 including study design and execution, medical monitoring, interpretation and reporting of the clinical trial results with the highest standards for safety and regulatory compliance.

How you will make an impact:

• Lead the medical strategy for assigned oncology programs
• Author clinical protocols (Phase 1-2), contribute to investigator brochures, IND/CTA submission, clinical study reports (CSRs), and regulatory documents throughout the program lifecycle
• Serve as the Medical Monitor for assigned trials, overseeing patient eligibility, safety, and protocol adherence
• Interpret clinical trial data, including safety, efficacy, PK, PD, and translating findings into actionable development strategy
• Ensure all clinical development activities are conducted in accordance with GCP, regulatory requirements, and company SOPs
• Serve as the primary clinical contact for assigned programs to internal teams, external investigators, and regulatory agencies
• Establish and maintain a collaborative relationship with medical experts and investigators in the assigned therapeutic area of developmen
• Collaborate closely with cross-functional teams, including Translational Science, Clinical Operations, Regulatory Affairs, Biostatistics, and Corporate Development
• Develop publications, and present data and strategy to governance committees and at external meetings

Who you are:

• MD, DO or equivalent degree. Board certification or eligibility in Oncology or Internal Medicine preferred
• 3+ years of clinical development and leadership experience in the pharmaceutical or biotechnology industry
• Proven track record in the design, execution, and analysis of Phase 1-2 clinical trials
• Excellent communication, presentation, and interpersonal skills, capable of influencing strategy across all levels of the organization
• Experience with biologic agents (mAb, ADC, TCE)
• Experience leading regulatory interactions (FDA, Health Canada, EMA)
• Experience with translational medicine and biomarker development

What we offer:

AbCellera’s hiring range for this role is CAD $280,000 - $325,000 annually, commensurate with your education and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. 

You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera:

Creating medicines is the most important work we can do. 

We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply:

Please submit your application through our website and refer to Job ID 23347 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

We are always interested in expanding our teams with top talent: currently focused on hiring for Protein Science, Drug Development, Manufacturing, and Quality. Also interested in people who can meaningfully contribute to these teams: Translational Biology, Engineering, Bioinformatics, Machine Learning, IT, Laboratory Management, and Software Development. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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