I am a Biomedical engineer with a focus on Quality and Regulatory Affairs, particularly in the implementation and improvement of maangement systems aligned with ISO 9001 and ISO 13485 standards.
I have contributed to QARA projects in both medical device and pharmaceutical environments, working on documentation structuring, regulatory compliance, and preparation for audits.
I joined nexialist in 2025 to support manufacturers in clarifying, organising, and optimising their quality systems.