Maintain and enhance the Quality Management System (QMS) in line with ISO 13485 .
Ensure all departments comply with ISO procedures , keeping documentation audit-ready.
Manage SAHPRA license compliance and update medical device files with current certifications.
Oversee corrective actions, risk assessments, and supplier database updates .
Liaise with suppliers, customers, and industry bodies to ensure regulatory compliance.
Assist in product registrations, failure reporting, and returns processing . […]
Support import/export compliance and assist with stock takes & cycle counts .
Update supplier...