Elevate clinical quality assurance as the Director at Xenon Pharmaceuticals in Vancouver or Boston. Leverage extensive GMP experience in managing quality for clinical programs.

Join the highly collaborative Quality GMP team at Xenon, focusing on clinical stage products and compliance with cGMP standards. You will utilize your leadership skills to interact with both internal staff and external partners, ensuring quality program requirements are met in a fast-paced environment.

Key Responsibilities: • Manage quality for manufacturing, testing, and release processes • Lead external quality activities, including batch reviews and audits • Collaborate on clinical programs to ensure compliance • Author and review quality-related documents and agreements • Represent quality at project and operational meetings

Requirements: • Bachelor’s degree in life sciences with 10+ years in GMP roles • Strong understanding of small molecule manufacturing • Extensive GxP knowledge...