Senior Validation Lead - cGMP & FDA Compliance
Salas O’Brien, Inc.
A full-service engineering firm seeks a Lead Validation Specialist in Cincinnati, OH. The role involves conducting audits, developing validation protocols, and leading project teams to ensure compliance with FDA regulations. Candidates should have a Bachelor's degree and 5-7 years of relevant experience along with strong analytical and communication skills. This position requires moderate travel and work in various settings including office and manufacturing environments. #J-18808-Ljbffr Salas O’Brien, Inc.
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