Develop and implement the R&D Quality Management System (QMS) to ensure compliance with global regulatory requirements
Provide strategic oversight for quality across the R&D pipeline and manage quality oversight for clinical batch releases
Lead issue management and partner with cross-functional teams to drive quality strategies that accelerate product development
Required Qualifications
Bachelor's degree in science, pharmacy, or a related field
Minimum 10 years of experience in pharmaceuticals, biopharmaceuticals, or vaccines manufacturing and quality operations
At least 5 years of direct experience in regulatory compliance and quality management
Proven leadership experience, including managing teams and serving on leadership committees
PhD in a relevant scientific discipline is preferred
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