Senior Validation & CQV Engineer — GMP Focus, Life Sciences
Listed on 2026-10-07
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Quality Assurance - QA/QC
Quality Engineering
Verista seeks a Senior Validation / CQV Engineer to author, edit, and execute validation documentation for standard equipment, systems, software, and processes as directed by project leads. You will run test scripts, maintain detailed records, and ensure compliance with GMP and Good Documentation Practice.
Candidates should have a Bachelor's degree, 5+ years in validation, strong communication, teamwork, and proficiency in Word, Excel, and PowerPoint.
Are you ready to take on the Senior Validation & CQV Engineer — GMP Focus, Life Sciences role at Verista?
We are looking to fill the Senior Validation & CQV Engineer — GMP Focus, Life Sciences position at Verista in Columbus, OH, United States.
The Senior Validation & CQV Engineer — GMP Focus, Life Sciences role at Verista is now open for applications in Columbus, OH, United States.
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