Post-Market Quality & Compliance Specialist

A leading medical device company based in North Carolina is seeking a Post Market Surveillance Specialist. This role involves managing the complaint handling process, ensuring compliance with FDA regulations, and creating documentation related to quality systems. The ideal candidate should have 3-5 years of experience in the pharma or medical device industry, with strong skills in communication and documentation management. The position offers a comprehensive benefits package and opportunities for career growth. J-18808-Ljbffr