Senior CQV Engineer On-Site Bioprocess Validation
Listed on 2026-10-16
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Engineering
Quality Engineering, Pharma Engineer, Validation Engineer, Process Engineer
Verista is seeking a Commissioning and Qualification Engineer to support installation, startup, commissioning and qualification of new single-use bioprocess equipment. You will collaborate with Process Engineering, Automation, CSV, Quality, equipment vendors and Operations to translate process requirements into qualification testing.
The role requires on-site work in Devens, MA, with a focus on IQ/OQ documentation, FAT/SAT activities and robust traceability across systems.
This is a great position to take on the Senior CQV Engineer On-Site Bioprocess Validation role at Verista.
Step into the Senior CQV Engineer On-Site Bioprocess Validation role at Verista in Harvard, MA, United States and grow with us.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Harvard, MA, United States.
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