Would you like to be in a business where you can make a difference - where your every effort and activity are recognized, where you contribute and develop the company? […]
Manage the Italian subsidiary Quality Systems primarily in accordance with ISO 13485 – MDR regulation (Medical Devices) and cGDPs (Pharma). […]
Handle deviations and non-conformities detected, ensuring the quality of the product output and verifying the effectiveness of the corrective actions taken.
Handle customer complaints with related investigation, corrective activities, response and closure complaints. […]
Lead and participate...