What are the responsibilities and job description for the Regulatory Affairs Specialist - Compliance Expert position at IntePros?
Job Overview
A Regulatory Affairs Specialist is required to join our Medical Device client in developing and submitting regulatory documentation for Class II and III products. The ideal candidate will have expertise in drafting, submitting, and gaining clearance for 510(k) submissions, as well as approval for IDE/PMA submissions to the FDA.
A Regulatory Affairs Specialist is required to join our Medical Device client in developing and submitting regulatory documentation for Class II and III products. The ideal candidate will have expertise in drafting, submitting, and gaining clearance for 510(k) submissions, as well as approval for IDE/PMA submissions to the FDA.
