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Aseptic GMP Production Coordinator
Job Description & How to Apply Below
A leading pharmaceutical company based in Brentwood, Missouri, is seeking a Production Assistant to support manufacturing activities, ensuring compliance with cGMP regulations. The ideal candidate will have a High School Diploma or Associates Degree, alongside 1-3 years of relevant experience. Responsibilities include conducting GMP audits, reviewing production documentation, and training personnel. The position demands effective communication skills and the ability to work within diverse teams.
The role supports a culture of continuous improvement in production processes.
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