Lead Medical Device Validation Engineer; IQ/OQ/PQ CSV
Listed on 2026-10-07
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Engineering
Biomedical Engineer, Medical Device Industry, Quality Engineering, Validation Engineer
The Sentio Group in Minneapolis, MN is seeking a Validation Engineer to help expand US manufacturing capacity in a leading Class III medical device company. This role involves owning equipment, process, and computer system validation in a regulated cleanroom environment.
With a focus on writing protocols and executing validation tasks, you will collaborate with Quality and Manufacturing Engineering teams, ensuring compliance with ISO 13485 and 21 CFR 820. The position offers a competitive hourly rate of $110 - $140.
Are you ready to take on the Lead Medical Device Validation Engineer (IQ/OQ/PQ CSV) role at The Sentio Group?
We are seeking a motivated Lead Medical Device Validation Engineer (IQ/OQ/PQ CSV) to join The Sentio Group in Minneapolis, MN, United States.
Consider building your career as a Lead Medical Device Validation Engineer (IQ/OQ/PQ CSV) at The Sentio Group.
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