Quality Process Validation Lead
Listed on 2026-10-18
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Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist, Production QC/QA
Ultralife Manufacturing USA seeks a Quality Engineer to ensure compliant manufacturing quality, lead investigations, validate test methods, and drive CAPA effectiveness. You will coordinate validations with Design and Manufacturing Engineers, review changes to specs and drawings, and mentor 1–3 technicians/inspectors while collaborating with suppliers and other teams.
The candidate should have 2–5 years' QA experience, working knowledge of ISO/QSR/UL, and strong communication skills.
The Quality Process Validation Lead role at Ultralife Manufacturing USA is now open for applications in Raynham, MA, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, Engineering.
The advertised compensation is 80..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Quality Process Validation Lead role in the description above.
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