Med Device QA & Compliance Specialist – Onsite
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Quality Assurance - QA/QC
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Healthcare
Job Description & How to Apply Below
Ledgent Technology in Tustin, CA is seeking a detail-oriented Quality Compliance Specialist to maintain our QMS for Class II medical devices. The role ensures development, manufacturing, and post-market activities comply with FDA 21 CFR Part 820, ISO 13485:2016, and EU MDR, acting as the primary compliance champion between engineering, operations, and regulatory teams.
This 6-month consulting engagement is 100% onsite, with compensation up to $41 per hour.
This is a strong role to take on the Med Device QA & Compliance Specialist – Onsite Contract role at Ledgent Technology.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Tustin, CA, United States.
This opportunity is part of our work in Legal, Management & Operations.
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