Quality Specialist – ISO/FDA Compliance | On-Site
Listed on 2026-10-06
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager, Production QC/QA
Eightelevengroup in St. Louis, MO is seeking a Quality Specialist for an on-site role to support quality functions and ensure compliance with ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, and EU MDR.
The position coordinates document control, calibration, audits, and quality data tracking to drive continuous improvement. The role requires experience in regulated industries, strong knowledge of quality management systems, and the ability to collaborate across teams to maintain compliance
Step into the Quality Specialist – ISO/FDA Compliance | On-Site role at Eightelevengroup in St. Louis, MO, United States and grow with us.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in St. Louis, MO, United States.
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