CQV Engineer: Pharma Clean Room Validation Lead
Stellent IT LLC
Stellent IT LLC is seeking a CQV Engineer to lead Clean Room qualification processes in Miami, FL. The role involves authoring and executing validation documentation, overseeing smoke studies, and performing temperature mapping. The ideal candidate should have a Bachelor's Degree, experience in pharmaceutical Clean Room environments, and strong problem-solving skills. The position offers the opportunity to work on critical validation activities in a dynamic environment. #J-18808-Ljbffr Stellent IT LLC
Vacancy posted 2 days ago
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