Senior Validation Engineer - CQV Life Sciences
Listed on 2026-09-22
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Engineering
Validation Engineer, Quality Engineering, Pharma Engineer
Verista, Inc. is seeking a Senior Validation / CQV Engineer in the United States to author, edit, and execute commissioning, qualification, and validation documentation for standard equipment, systems, software, and processes as part of a project team.
You will run test scripts, maintain detailed records, and ensure adherence to schedules while collaborating with peers in regulated packaging environments. A Bachelor’s degree and 5+ years of CQV experience, GMP training, and proficiency with
For the Senior Validation Engineer - CQV for Life Sciences position at Verista, Inc., we are reviewing applications now.
Are you ready to take on the Senior Validation Engineer - CQV for Life Sciences role at Verista, Inc.?
We would love to welcome a new Senior Validation Engineer - CQV for Life Sciences to our group in NC, United States.
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