Validation Engineer – Medical Device Quality & PPAP Lead
Listed on 2026-10-16
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Engineering
Quality Engineering, Biomedical Engineer -
Quality Assurance - QA/QC
Quality Engineering
Weiss-Aug in Fairfield, NJ seeks a Validation Engineer to lead PPAP/Validation deliverables for new programs, ensuring ISO
13485, 21 CFR 820, GMP compliance. You will write IQ/OQ/PQ protocols, support APQP docs, and drive quality improvements across programs.
The role requires a 4-year engineering degree and medical device quality experience, with opportunities to contribute to innovative, vertically integrated manufacturing solutions in the US.
We would love to welcome a new Validation Engineer – Medical Device Quality & PPAP Lead to our group in Fairfield, NJ, United States.
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 Fairfield, NJ, United States.
This opportunity is part of our work in Engineering.
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