About this opportunity
Verista, Inc. lists this CQV Engineer Lead - Pharma Equipment Validation opportunity in bloomington, Indiana. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Verista, Inc. is seeking engineers in Bloomington, IN to support commissioning, qualification, and validation of manufacturing equipment for life sciences clients.
You will work with project teams to install, test, and certify equipment, ensuring cGMP compliance and thorough documentation. Ideal candidates have 5+ years of CQV experience and a strong background in FAT/SAT, IQ/OQ/PQ, and P&ID interpretation.
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Worksite address
bloomington, IN, 47401, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.