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 i...