Manufacturing Bioprocess Technician

AbCellera is breaking the barriers of conventional drug development to propel antibody-based medicines from target to clinic. We are a team of scientists, engineers, creatives, and business professionals who believe that advancing science enhances lives. We have developed technologies to unlock high-value drug targets, including antibody-drug conjugates and T-cell engagers for cancer, and complex transmembrane proteins for indications such as metabolic and endocrine conditions, pain, and autoimmunity.

We are looking for a highly motivated and dynamic Manufacturing Bioprocess Technician to join our clinical manufacturing team. You will join a team responsible for the production of antibody therapeutics working in a new GMP manufacturing facility. In this role, based in beautiful Vancouver, Canada, you will interface with automated production systems and controls to maintain the facility in a high state of inspection preparedness and to contribute to inventory and process management.

How you might spend your days

• Supporting manufacturing processes and continuous improvement initiatives for cell line initiation (vial thaw), cell line scale-up, bioreactor operations, harvest clarification, TFF, column packing, chromatography, bulk drug substance fill, media and buffer preparation, weigh and dispense operations and drug product filling
• Performing basic maintenance tasks on equipment under supervision, as well as monitoring manufacturing processes and identifying abnormalities or deviations
• Authoring and revising cGMP documentation (batch records, protocols, SOPs) and performing periodic reviews of cGMP documentation to ensure accuracy 
• Assisting in the cleaning and sanitization of manufacturing areas, documenting manufacturing activities and data entry
• Assisting in the implementation of manufacturing systems and processes that are technically sound, and promoting effective and efficient operations
• Supporting or leading investigations related to the manufacturing process, and authoring deviations, non-conformances, and CAPAs as required
• Contributing to and assisting with facility audits from the FDA, Health Canada, and other regulatory bodies during facility audits

We’d love to hear from you if

• You have a technical college certificate and a minimum of 2 years of GMP manufacturing experience, ideally in a cleanroom environment or a Bachelor’s degree in a relevant scientific discipline 
• You are strongly self-motivated and are able to identify project needs and follow that up with building and implementing solutions
• You are passionate about building and implementing a "Right First Time" culture to meet cGMP requirements for clinical material
• You have a good mechanical aptitude; knowledge of upstream and/or downstream processing techniques is also a strong asset
• You have experience ensuring timely execution and review of procedures, batch documentation, logbooks, deviations, CAPAs, change controls, and completion of ERP orders
• You are energized by working with teammates to contribute to the development of innovative medicines in various therapeutic areas

What we offer

AbCellera’s hiring range for this role is CAD $57,000 - $71,300 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. 

We have a number of ways to support AbCellerites in maximizing their work-life synergy. You will have a $1,500 annual Active Lifestyle Allowance, annual vacation, the opportunity for flexible work arrangements, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find abundant teams and social groups to build community and connections across AbCellera.

About AbCellera

AbCellera is a global company that discovers and develops antibody-based medicines that help people live longer, happier, and more productive lives. We are focused on bringing innovative medicines to patients, both by advancing our internal pipeline of programs and partnering with companies that have novel science or innovative technology.

And it all starts with our team. We’ve built a place where people feel they are part of something bigger than themselves. A place that exists to push the limits of science and technology, and aims to bring better therapies to patients.

We look for people with drive and energy. Idealists. People we love and people we trust. This may be unconventional, but it is the key to our success. 

To apply

Please submit your application through our website and refer to Job ID 23275 in your cover letter. We apologize in advance, but we receive a large volume of applications and are only able to contact those who are selected for an interview.