QA/RA Specialist — Path to Leadership in Med Devices

Il y a 2 heures

Antwerp, Flanders, Belgique Nuwhï bv Temps plein

Nuwhï bv in the Antwerp region is seeking a QA/RA Specialist to strengthen the quality and regulatory framework for medical devices. You will work with the existing QA team to ensure products, processes and documentation meet ISO 13485 standards and EU MDR requirements.

This role offers growth toward broader leadership responsibilities, with exposure to audits, regulatory filings, and collaboration with manufacturing partners across Europe.