Regulatory Affairs Specialist Certification Jobs

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Medical Device Quality Engineer I  

Anatomage, Inc. - Santa Clara, California

We Look For Experience with Medical Device Software and Hardware Experience with QMS/eQMS Knowledge of ISO 13485 / MDSAP Global regulatory affairs experience (FDA, MDD/CE/MDR, UKCA, etc.) Document Control

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from: resume-library.com (+1 source) - 24 days ago


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