Ensure product compliance with ISO 13485 and MDR standards.
Review technical procedures and documentation and verify compliance.
Actively participate in inspection and audit activities (internal/external).
Follow up and analyze non-conformities and take corrective and preventive actions.
Collaborate with production and procurement teams to ensure quality from source to finished product.
Train and guide work teams on quality policies and procedures.
Bachelor's degree in science or engineering (preferably in medical or industrial specializations).2-4 years of experience in quality assurance within medical supplies factories.Good knowledge of quality systems: ISO 13485 – GMP – CAPA.