Post Market Surveillance Specialist at Intuitive

Intuitive is hiring a Regulatory Post Market Surveillance Specialist to investigate medical device complaints, classify and escalate issues, conduct failure analysis, file malfunction MDR reports, evaluate documentation, create customer response letters, and manage complaint backlogs. The role requires a degree in engineering, life science, or an equivalent field, English proficiency at 85%, and at least two years of medical device experience, including knowledge of complaint files, quality records, and regulatory reporting requirements.