Quality Documentation Auditor – Medical Devices
Listed on 2026-10-06
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Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
Exalta Group in Marquette, MI is seeking a Quality Systems Associate to ensure accuracy and compliance of manufacturing documentation by auditing routers, DHRs, and related records. This role requires strong knowledge of GDP, FDA regulations, ISO 13485, and good documentation practices to support continuous improvement within the QMS.
You will review production records, verify traceability, identify discrepancies, and coordinate corrective actions with Manufacturing, Quality, and Engineering
This is a great role to take on the Quality Documentation Auditor – Medical Devices role at Exalta Group.
All applications are reviewed carefully by our team.
The position is based in Marquette, MI, United States.
This opportunity is part of our work in Management & Operations, Engineering.
The advertised compensation is 28.000 - 37.000.
We aim to respond to suitable candidates as soon as possible.
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