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Quality Assurance Specialist I - GMP & Clinical Trials

Regulatory Toolkit

Catalent is seeking a Quality Assurance Specialist I for our Kansas City, MO site to support clinical trial projects and ensure compliance with GMP and regulatory requirements. You will maintain accurate documentation and contribute to quality assurance processes across the product lifecycle in a 12:00pm–8:00pm shift, onsite. Responsibilities include participating in continuous improvements, preparing Certificates of Analysis, and ensuring timely, compliant records and procedures. #J-18808-Ljbffr Regulatory Toolkit

Vacancy posted 2 days ago
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