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cGMP Consulting Inc. seeks an experienced senior leader to manage multiple validation and qualification projects across equipment, utilities, facilities, systems, and processes in a GMP environment. The role offers significant autonomy and cross-functional leadership to influence operations in a fast-paced, regulated manufacturing setting. The ideal candidate brings deep cGMP experience, FDA regulatory knowledge, and a track record of delivering thorough protocols, reports, and CAPA-driven

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Level

Manager L7

Location

Dayton, OH

Occupation

Validation Engineers

Industry

Pharmaceutical Preparation Manufacturing

Posted

4 days ago

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