Job Description
Lead GMP quality assurance efforts as Director at Xenon Pharmaceuticals, located in Vancouver or Boston. Seek excellence in clinical program quality management.
As part of the Quality GMP team at Xenon, you will ensure quality standards are met throughout all stages of development for innovative biopharmaceuticals. Your role involves collaboration with various departments and the management of external quality activities, making your leadership crucial for success.
Key Responsibilities:
• Responsible for clinical stage product quality and compliance
• Direct quality-related activities with Contract Manufacturing Organizations
• Align internal goals with quality best practices and policies
• Author and approve essential quality documentation
• Attend key team meetings, providing quality insights
Requirements:
• Bachelor’s degree in life sciences and over 10 years in GMP
• Strong grasp of small molecule manufacturing processes
• Familiarity with early pha...
As part of the Quality GMP team at Xenon, you will ensure quality standards are met throughout all stages of development for innovative biopharmaceuticals. Your role involves collaboration with various departments and the management of external quality activities, making your leadership crucial for success.
Key Responsibilities:
• Responsible for clinical stage product quality and compliance
• Direct quality-related activities with Contract Manufacturing Organizations
• Align internal goals with quality best practices and policies
• Author and approve essential quality documentation
• Attend key team meetings, providing quality insights
Requirements:
• Bachelor’s degree in life sciences and over 10 years in GMP
• Strong grasp of small molecule manufacturing processes
• Familiarity with early pha...
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