Pharma Label Specialist II — GMP & Documentation
Catalent
Catalent’s Kansas City facility seeks a Label Specialist II to support label creation, inspection, and distribution for clinical and commercial packaging. The role ensures regulatory compliance, GMP adherence, and meticulous documentation in a 7:30am-4:00pm, onsite environment in Kansas City, MO. Responsibilities include managing label documents, inspecting multiple panels and languages, exporting clinicopia data, and maintaining label control records. #J-18808-Ljbffr Catalent
Vacancy posted 3 days ago
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