Senior CQV Engineer: Pharma Validation Lead; Onsite Indy
Job in
Columbus, Franklin County, Ohio, 43224, USA
Listed on 2026-07-25
Listing for:
Verista
Full Time
position Listed on 2026-07-25
Job specializations:
-
Engineering
Validation Engineer, Pharma Engineer, Quality Engineering
Job Description & How to Apply Below
Verista is seeking a Senior CQV Engineer to design validation plans, conduct risk assessments, and document qualification activities for pharmaceutical manufacturing.
You will lead CQV tasks, write and review validation documentation, and ensure compliance with GMP standards while coordinating with project teams.
The role requires on-site work in the Indianapolis area, 10–50% travel, and 4–6 years of CQV experience. A Bachelor's degree is required.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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