Advance your career with Xenon Pharmaceuticals as the Associate Director of Quality Control in Vancouver, BC. Lead critical QC activities for both clinical and commercial drug programs while adhering to ICH and cGMP standards.

In this pivotal role, you will oversee quality control efforts concerning the stability and release of drug substances and products. Your expertise in small molecules will guide analytical testing, specifications, and investigations throughout the drug lifecycle. Collaborate with various internal and external teams to ensure high-quality standards and compliance.

Key Responsibilities:



• Manage master specifications for clinical and commercial programs • Lead stability activities and evaluate stability data trends • Draft reports for out-of-specification results • Review analytical results for product release • Ensure effective collaboration with external laboratories

Requirements: • 8+ years of relevant pharmaceutical industry experience • Strong background in quality control and stability programs • Experience with IND and BLA submissions preferred • Excellent communication skills and leadership experience • Willingness to travel up to 20% domestically and internationally

Utilize your quality control skills to ensure the success of recent therapeutic candidates at Xenon Pharmaceuticals. #J-18808-Ljbffr

📌 Quality Control Associate Director at Xenon (Winnipeg)
🏢 Xenon Pharmaceuticals
📍 Winnipeg