Quality Engineer - Medical Device Validation & Compliance
Listed on 2026-10-06
-
Engineering
Quality Engineering, Biomedical Engineer, Regulatory Compliance Specialist -
Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist
AJR Enterprises, a UFP Technologies company, is seeking a Quality Engineer in St. Charles, IL to support compliance and quality assurance for medical device manufacturing.
You will work with operations, supply chain and NPD teams to ensure risk management, process validation and CAPA are effectively implemented. Qualifications include a science/engineering degree and 3–7 years in medical device QA; experience with ISO 13485 and FDA Part 820 is required.
The Quality Engineer
- Medical Device Validation & Compliance role at UFP Technologies is now open for applications in St. Charles, IL, United States.
Learn more about the Quality Engineer
- Medical Device Validation & Compliance role in the description above.
We appreciate your interest in this position.
Join UFP Technologies and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
(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).