About this opportunity
Verista lists this GMP Validation Engineer for Life Sciences Equipment opportunity in columbus, Ohio. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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.
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Worksite address
columbus, OH, 43224, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.