Quality Engineer - Medical Devices & Regulatory Compliance
Listed on 2026-10-17
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering
Medline Industries, LP in Chicago seeks a quality-focused professional to independently set basic quality standards for in-process and lead methods for testing, sampling and training. You will evaluate production processes, recommend improvements, manage vendor qualification and maintain DMRs and CE technical files.
The role requires design of experiments, SPC expertise, and collaboration with regulatory groups to ensure compliance with 21 CFR 820 and ISO
13485.
We have an opening for a Quality Engineer - Medical Devices & Regulatory Compliance in Chicago, IL, United States within Bio & Pharmacology & Health, Engineering.
This opportunity is part of our work in Bio & Pharmacology & Health, Engineering.
The advertised compensation is 79..
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).