Description
The Quality Systems Specialist supports the development, implementation, monitoring, and continuous improvement of a medical device Quality Management System, including CAPA, design control, change control, document control, training records, device history records, audits, complaints, and quality control testing. The role is an individual contributor operating in both office and manufacturing environments, requiring a high school diploma, 2–5 years of quality systems experience, QMS experience, and strong computer, communication, and regulatory knowledge skills.
