ISO Quality & Validation Engineer — Medical Devices
Listed on 2026-10-17
-
Engineering
Quality Engineering, Biomedical Engineer -
Quality Assurance - QA/QC
Quality Engineering
Sterling Engineering is seeking a hands-on Quality Engineer to support manufacturing validation and quality process development in a regulated environment. The role focuses on IQ/OQ/PQ validations, in-process controls, and batch release procedures to ensure readiness for production.
The ideal candidate will build validation systems from the ground up, assess risks, and collaborate with Manufacturing, Engineering, and Product Development teams to deliver reliable quality systems and improved
The ISO 13485 Quality & Validation Engineer — Medical Devices position in the Engineering field is open for applications.
The position is based in Chicago, IL, United States.
This opportunity is part of our work in Engineering.
The advertised compensation is 70..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).