QMS Specialist: ISO 13485 & FDA Compliance

A leading clean tech startup is seeking a QMS Specialist in Florida to implement and audit quality systems ensuring compliance with ISO 13485 and FDA QSR requirements. The ideal candidate will bring over 3 years of Quality Management experience, especially in Class II medical devices. Responsibilities include owning the electronic QMS tool, conducting internal audits, and supporting regulatory inspections. Join a passionate team dedicated to innovating air purification technology. #J-18808-Ljbffr