Search the 5 jobs at AbCellera

As a Senior Scheduler at AbCellera, you will manage the master integrated schedule for a GMP clinical manufacturing facility. Responsibilities include maintaining the schedule, facilitating planning meetings, developing scenarios for decision making, and collaborating with teams to improve schedule performance.

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.

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.

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.