GMP Validation Engineer for Life Sciences Equipment
Verista
Verista in the life sciences sector is seeking a Validation/CQV Engineer to author, edit, and execute commissioning, qualification, and validation documentation for standard equipment and processes. The role requires a Bachelor's degree, strong teamwork, documentation discipline, and experience with GMP and validated testing. Ohio/Columbus area; US salary ranges apply with competitive benefits. #J-18808-Ljbffr Verista
Vacancy posted 4 days ago
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