Senior Validation Engineer - cGMP & Qualification Lead
Dormont Manufacturing Co
Dormont Manufacturing Co in New York is seeking a Validation Engineer IV to oversee validation activities for cGMP pharmaceutical and medical device manufacturing. The role includes authoring validation plans, reviewing system documentation, and developing risks strategies. The ideal candidate has a Bachelor's degree in Engineering with at least 8 years in the pharmaceutical industry, strong technical writing skills, and ability to work autonomously while communicating effectively across functions. #J-18808-Ljbffr Dormont Manufacturing Co
Vacancy posted 1 day ago
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