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Aseptic GMP Production Coordinator CI
Job Description & How to Apply Below
Location: Brentwood
A pharmaceutical company in Brentwood, Missouri is seeking a Quality Assurance Associate to assist production management with various responsibilities, including performing GMP audits, reviewing production documentation for compliance, and coaching colleagues on cGMP regulations. Candidates should have 1-3 years of relevant experience and a High School Diploma or Associates Degree. This is a full-time position requiring adherence to aseptic processes and safety protocols.
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