CQV Engineer: Equipment Validation Specialist
Arcadis
A global EPCM firm is seeking a CQV Engineer to support projects in New Bedford, MA. The role involves developing and executing equipment validation protocols within a cGMP and FDA regulated environment. Candidates should have 3-5 years of Equipment Validation experience and a strong understanding of automated systems. The position also requires preparation of validation documentation and resolution of validation-related issues, ensuring compliance with industry standards. #J-18808-Ljbffr Arcadis
Vacancy posted 1 day ago
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