Novo Nordisk
GMP Batch Documentation & Quality Records Specialist
Novo Nordisk, Clayton, North Carolina, United States, 27520
A global healthcare leader in North Carolina is seeking a routine support professional for batch and documentation review processes. The ideal candidate should have an Associate's Degree in a relevant field along with experience in a GMP regulated environment. The role focuses on ensuring compliance with production documentation and supporting continuous process improvement. Join us in making a real impact in healthcare with your expertise.
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