Hajar Channouf

Participation in the development and monitoring of regulatory and quality assurance documents for medical devices. Updating of these medical devices with the Health Products and Safety Monitoring.

Acquired practical skills in molecular biology techniques applied in a clinical setting. Gained experience handling and processing clinical samples according to strict safety protocols.

Performed routine inspections and maintenance of medical devices. Ensured compliance with safety and regulatory standards.

Focus on regulatory affairs and quality assurance, gaining advanced knowledge of ISO standards and risk management.

Specialized in disease mechanisms and immune responses, equipping me with a strong foundation for biomedical and clinical research.