Onsite Quality Systems Specialist - Medical Devices
Listed on 2026-09-30
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Quality Assurance - QA/QC
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Healthcare
Vital Path seeks a Quality Systems Specialist to support the execution and maintenance of a harmonized quality management system across multiple manufacturing sites in a regulated medical device environment.
You will coordinate document control, training compliance, CAPA coordination, change control administration, and audit readiness activities, partnering with cross-functional teams to ensure compliance with FDA, ISO 13485 and internal requirements.
Join us at Vital Path as our next Onsite Quality Systems Specialist - Medical Devices in MN, United States.
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 MN, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, IT & Technology.
The advertised compensation is 70.000 - 82.000.
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