Location: Vancouver.
Employment type: full-time.
Key skills: GMP, cGMP, Quality Control, FDA Regulations.
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're looking for an experienced Associate Director/Senior Manager, QA Operations to lead Quality oversight for our biological Drug Substance clinical manufacturing facility (Brightfield) in Vancouver. You'll provide real-time Quality support to cGMP manufacturing, warehousing, and distribution operations, ensuring activities meet regulatory expectations and industry best practices — all while driving continuous improvement and building a strong culture of quality across the site. If you are someone with deep technical expertise in Quality and hands-on GMP leadership experience, who can partner effectively across…