2 Stellenangebote

Ensures that the Site Quality System is effective in meeting defined requirements and reports the performance to management as well as the compliance with applicable company, ISO, FDA and other regulatory and local policy requirements;...

Creating and updating technical documentation for CE Mark in accordance with EU MDR 2017/745; Person Responsible for Regulatory Compliance (PRRC) per Article 15 EU MDR 2017/745; Providing regulatory guidance during the entire life cycle of Medical;...