Quality engineer
SligoCollins McNicholas
...the Role: Degree in science or engineering. 3–5 years’ experience in medical devices. Strong knowledge of ISO 13485 and FDA 21 CFR 820. Strong understanding of MDR and FDA submissions. Auditing experience (internal/external) is a plus. Validation experience (sterilization, process, packaging) is a plus. Knowledge of cGMP [...]
Category Manufacturing & Production
30 days ago in Collins McNicholas