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Director CMC Drug Product - Xenon Pharmaceuticals
Job Description & How to Apply Below
As a Director at Xenon, you will guide the drug product process from development to commercial distribution, ensuring regulatory compliance and quality. This hybrid position allows for collaboration within a skilled CMC team, emphasizing the importance of successful partnerships with Contract Manufacturing Organizations. You will play a vital role in transforming scientific innovation into therapeutic reality.
Key Responsibilities:
• Manage late-phase process validation and commercialization
• Ensure high-quality standards within manufacturing processes
• Collaborate with external suppliers for drug supply
• Create and review regulatory submissions
• Contribute to stability and packaging strategies
Requirements:
• PhD in Chemistry, Engineering, or related area
• 10+ years in drug manufacturing management
• Background in solid oral dosage forms
• Knowledge of cGMP regulations
• Leadership in high-performing team development
Join Xenon Pharmaceuticals and lead the journey of transformative drug products towards commercialization.
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