Associate Director, Regulatory Affairs

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 Regulatory Affairs (RA) leader to join our growing team. You will implement  global regulatory strategies and develop CTA/IND submissions across AbCellera’s portfolio of innovative biologics-based therapeutics. As the primary point of contact with regulatory authorities, you will also provide expert regulatory guidance on nonclinical and clinical issues to program teams throughout a product’s life cycle. If you are a regulatory professional who wants to help move novel biologics from the lab to patients, we’d love to hear from you. 

How you might spend your days 

• Developing and implementing regulatory strategies for pipeline programs that highlight opportunities to accelerate development as well as identify regulatory risks and mitigation plans
• Developing and overseeing regulatory submissions and ensuring appropriate content in collaboration with project teams as well as clinical, nonclinical, translational, and project management functions
• Serving as the project team’s primary expert on regulatory matters, including new