Step into a pivotal role at Xenon Pharmaceuticals as Director of Quality Assurance, GMP, specializing in clinical program oversight. This position offers strategic impact in a hybrid work setting.

Xenon aims to enhance its Quality GMP team with a Director who will lead vital quality assurance processes for therapeutic drugs in development. This role facilitates collaboration across R&D, Manufacturing, and Quality teams, demanding an extensive background in cGMP compliance and quality systems. You will play a key role in shaping the quality culture within the organization.

Key Responsibilities: • Direct quality assurance for clinical manufacturing sites • Oversee external quality processes and compliance matters • Contribute to CMC discussions and quality reviews • Author quality agreements and system documentation • Represent Quality in project and inspection meetings

Requirements: • Bachelor’s degree in life sciences and 10+ years in quality • Expertise in s...