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Title Author
Manager, Regulatory Affairs and Quality Assurance (Medical Device Software) Written by Robert Fleming
RA/QA Manager Written by Robert Fleming
QA Audit Supervisor Written by Robert Fleming
QA Auditor Written by Robert Fleming
Regulatory Specialist I Written by Robert Fleming
Sr. Regulatory Affairs Specialist Written by Robert Fleming
Senior Regulatory Affairs Specialist Written by Robert Fleming
Senior Specialist, Regulatory Affairs - Critical Care Written by Robert Fleming
Manager, Regulatory Affairs (Sustaining) – Transcatheter Heart Valve Written by Robert Fleming
Senior Manager, Regulatory Affairs - Transcatheter Heart Valve Written by Robert Fleming
 
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