Pharma Compliance Specialist III - GMP & Documentation
Catalent, Inc.
Catalent’s Kansas City facility is seeking a Compliance Specialist III to support the preparation, review, and approval of technical and regulatory documentation onsite in Kansas City, MO. You will ensure compliance with current Good Manufacturing Practices and internal procedures, contributing to high-quality pharmaceutical operations. Key responsibilities include authoring and reviewing protocols and batch records, maintaining lab notebooks, and ensuring readiness for on-site clients within a #J-18808-Ljbffr Catalent, Inc.
Vacancy posted 2 days ago
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