Medical Device Validation Engineer PPAP & GMP
Listed on 2026-10-13
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Engineering
Quality Engineering, Biomedical Engineer, Pharma Engineer -
Quality Assurance - QA/QC
Quality Engineering
Weiss-Aug is seeking a passionate Validation Engineer for their Fairfield, NJ site. You will prepare master validation documentation, ensure GMP/ISO
13485/21 CFR 820 compliance, and drive PPAP/APQP activities across new medical device programs.
You will collaborate with cross-functional teams, lead audits, and ensure quality deliverables through robust validation and process control. This role demands strong technical writing and a solid engineering background.
We are seeking a motivated Medical Device Validation Engineer PPAP & GMP to join Weiss-Aug in Fairfield, NJ, United States.
We would love to welcome a new Medical Device Validation Engineer PPAP & GMP to our group in Fairfield, NJ, United States.
For the Medical Device Validation Engineer PPAP & GMP position at Weiss-Aug, we are reviewing applications now.
Step into the Medical Device Validation Engineer PPAP & GMP role at Weiss-Aug in Fairfield, NJ, United States and grow with us.
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