The Senior Manager, Upstream Site MSAT will lead the GMP scale purification of monoclonal and bispecific antibodies, focusing on process and facility design, technology transfer, and batch production in a new manufacturing facility. Responsibilities include providing technical leadership, managing scale-up processes, contributing to facility design, and ensuring compliance with cGMP requirements.

As the Senior Director of Quality Assurance, you will lead the establishment and management of the QA organization, develop quality systems to ensure compliance with regulations, mentor and build a cross-functional team, and oversee audits and vendor management processes. Your focus will be on driving quality initiatives across the drug development lifecycle, ensuring successful project progression from discovery to production.

In this role, you will implement, configure, and maintain the SAP S/4HANA system, working with business teams and IT to enhance operations in financial, procurement, and manufacturing areas, while acting as a subject matter expert and addressing data quality issues.

As a Bioinformatics and Protein Engineering Intern, you will execute workflows focused on therapeutic development related to genomics surveillance of viral pathogens and protein engineering. The role includes developing bioinformatics tools, evaluating antibody diversity, and visualizing data to inform scientific insights while collaborating with a diverse team of professionals.

The Senior Research Scientist will design and develop Modeling and Simulations to enhance drug development for antibody therapeutics. Responsibilities include collaborating with project teams, developing quantitative pharmacology models, and presenting findings to a varied audience. This role requires a strong background in mathematical modeling and pharmacology principles.

The QC Analyst in Microbiology will conduct microbiological testing in a cGMP environment, support aseptic product manufacturing, execute routine testing on utilities, evaluate test results, and contribute to method documentation. They will also assist with investigations related to microbiology lab discrepancies.

Join our team to contribute to various fields such as Protein Science, Drug Development, and Software Development. We seek talented individuals who can impact areas like Engineering, Bioinformatics, and Machine Learning.

The Principal Scientist will lead the development of pharmacokinetics capabilities, establish bioanalysis strategies, manage CROs, oversee assay development, prepare regulatory documents, and mentor junior scientists. The role demands a strong focus on antibody therapeutics and requires collaboration across teams.

The Scientist will enhance mass spectrometric capabilities, develop analytical methods, perform protein characterization, and ensure alignment with GxP expectations supporting CMC projects and therapeutic development.

As a QA Specialist at AbCellera, you will ensure compliance of clinical batch manufacturing with cGMP, author and review relevant documentation, participate in the quality event management process, and support risk assessments. Your efforts will help uphold standards and enhance operational excellence in drug development.