**Job Description Summary**
Maintain and continuously improve Quality Management System (QMS) processes to ensure compliance with medical device regulations in applicable countries. Act as the key contact for internal and external audits, facilitating smooth audit execution and driving corrective and preventive actions (CAPA) for identified nonconformities.
Support new product design transfer and mass production transfer activities; participate in design reviews at all stages; review and approve DMR-related documentation for medical devices; evaluate Equipment Qualification and Process Validation (EQ/PV); and take responsibility for routine compliance checks on the production line.
GE HealthCare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter . Unlock your ambition, turn ideas into world changing realities , and join an organization where every voice makes a difference, and every difference buil...