Analytical Equipment Engineer - CQV, GMP & Maintenance
Listed on 2026-10-18
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Engineering
Quality Engineering, Validation Engineer, Pharma Engineer, Process Engineer
Verista is a leading life sciences solutions provider with a strong customer focus in pharmaceutical and biotechnology manufacturing. We are seeking a Project Engineer to support analytical equipment, CQV activities, and ongoing operations across multiple facilities.
The role requires a Bachelor's degree in Engineering or related discipline and 5+ years of hands-on experience in GMP environments. Onsite work in Thousand Oaks, CA, five days a week, with a competitive salary and benefits package.
Are you ready to take on the Analytical Equipment Engineer - CQV, GMP & Maintenance role at veristainc?
The position is based in Thousand Oaks, CA, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, IT & Technology.
The advertised compensation is 85..
We aim to respond to suitable candidates as soon as possible.
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