AbCellera Biologics

You'll lead **QC data architecture and eSystems** for GMP-compliant laboratory operations at a **clinical-stage biotech company**. Your work ensures systems are fit-for-purpose, compliant, and enable efficient data-driven workflows. You'll have high ownership to build **scalable quality and digital capabilities** that impact drug development.

You'll operate and maintain hybrid IT infrastructure for a **clinical-stage biotechnology company**, working across cloud (AWS) and on-prem systems. Your core impact will be **automating routine tasks** and improving availability and efficiency. This generalist role offers variety from troubleshooting scientific system performance to automating processes.

You'll own and evolve the IT systems behind AbCellera's drug discovery pipeline, leading modernization across **hybrid cloud and on-prem environments**. You'll shape technical architecture, set direction, and stay hands-on with the systems you're responsible for.

You'll drive **bioanalytical and ADME strategies** for antibody drug conjugate programs, bridging discovery and clinic. Your work will directly support regulatory filings (IND/CTA) and project progression.

You'll design and monitor non-GLP/GLP toxicology studies, providing nonclinical safety support for early to late-stage programs at a biotech innovator. Your work will directly impact **IND/CTA/BLA submissions** and **regulatory strategy** across AbCellera's pipeline. This role offers a chance to lead **cross-functional program teams** and shape safety strategy.

You'll lead **microbiology operations** in a GMP environment, performing hands-on testing and troubleshooting alongside your team. You will own a program end-to-end from bench work to guiding analysts, ensuring inspection-ready labs and compliant microbial methods. This role offers deep technical mentorship and cross-functional collaboration at a **clinical-stage biotechnology company**.

You'll lead **microbiology QC operations** at a **clinical-stage biotech** developing antibody medicines. Your core impact is ensuring **inspection-ready labs** and smooth product testing. This role combines deep technical mentorship with cross-functional collaboration.

You'll lead **design and oversight of toxicology studies** for antibody-based medicines in a clinical-stage biotech, translating complex data into **clear risk-benefit evaluations** for project teams and executive leadership. You'll also **author regulatory documents** (INDs, CTAs, BLAs) and stay current with evolving guidance.

You'll design and execute **nonclinical safety studies** for **antibody-based drug candidates** at a clinical-stage biotech. Your work will directly impact the safety assessment of breakthrough medicines. You'll collaborate across teams to advance our internal pipeline.

You'll lead **microbiology operations** in a **GMP QC lab**, providing hands-on mentorship and running assays daily. Your core impact will be ensuring **inspection readiness** and timely release of medicines for patients.

Vous planifierez, dirigerez et superviserez des **études cliniques** de bout en bout, en assurant conformité réglementaire et respect des délais. Vous collaborerez avec des équipes interfonctionnelles pour générer des **données cliniques de haute qualité**.

You'll oversee **in vivo studies** supporting **therapeutic antibody discovery** at a clinical-stage biotech. Your work directly impacts pipeline advancement. This role offers deep technical mentorship and cross-functional collaboration.

You'll lead **non-clinical safety strategy** for AbCellera's pipeline, designing and overseeing toxicology programs to support **regulatory submissions** worldwide. Your expertise will directly guide candidate selection and risk assessment, driving **innovative antibody therapeutics** from discovery through development.

You'll support **quality systems and documentation** for a biotech company developing antibody-based medicines. You'll manage records, write **SOPs**, and help keep our processes audit-ready. This 12-month contract offers hands-on experience in **quality assurance** within a regulated environment.

You'll perform daily health assessments and handle animals for therapeutic antibody discovery at a **clinical-stage biotechnology company**. You'll ensure facility cleanliness, organize lab spaces, and collaborate with teammates to tackle challenging scientific problems. This role offers **hands-on experience in a fast-paced research environment**.

You'll join our Clinical Development team to **drive clinical strategy for oncology programs** from pre-IND through Phase 1-2. You'll provide **medical leadership** ensuring safety and regulatory compliance. This role offers the chance to **shape early-stage therapies** at a fast-growing biotech.

You'll join the Engineering Asset Management team to execute CQV and engineering compliance activities in a GMP environment. Your work ensures systems meet regulatory standards for **antibody-based medicine manufacturing**. This role offers **ownership of deviation investigations** and **cross-functional audit support**.

You'll lead the clinical development strategy for antibody-based medicines in endocrinology and autoimmune diseases from pre-IND through late-stage trials. You'll drive **study design, execution, and regulatory submissions** for our pipeline programs. This role offers the chance to **shape cutting-edge therapies** at a clinical-stage biotechnology company.

You'll lead **microbiology operations** and provide **in-lab mentorship** in a GMP QC environment at a **clinical-stage biotechnology company**. You'll ensure inspection readiness and drive contamination investigations.

You'll support the design, implementation, and ongoing management of the **Quality Management System** for QC-related CMC/GMP activities. Your role ensures that QC laboratory electronic systems are **fit-for-purpose and compliant**, enabling efficient, data-driven laboratory operations. You'll be empowered with a high degree of ownership to **build scalable quality and digital capabilities**.

You'll support central services essential to manufacturing operations at a **biotech company**. You'll sanitize equipment, schedule cleaning, and manage inventory to ensure smooth production. This 9-month contract offers exposure to a **highly regulated GMP environment**.

You'll lead and manage clinical trials from start-up through completion, collaborating with cross-functional teams to deliver high-quality data. You'll ensure **regulatory compliance** and adherence to timelines and budgets. This role offers the chance to impact **antibody-based medicine development** at a clinical-stage biotech company.

You'll serve as a **trusted Quality partner** on the cleanroom floor, providing **real-time GMP oversight** for Drug Substance manufacturing operations at AbCellera. You'll lead the development and implementation of quality systems, drive quality event management, and support clinical batch disposition. This role offers a unique chance to **shape quality operations** during a pivotal growth stage.

You'll perform **in vivo** and **ex vivo** techniques** to support antibody discovery and efficacy assessments at a clinical-stage biotech. You'll ensure high-quality study execution and animal welfare while collaborating with research teams. The role offers mentorship and a strong scientific community.