Quality engineer
SligoCollins McNicholas
...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 and medical device manufacturing is a plus. Understanding of ISO [...]
Category Manufacturing & Production
30+ days ago in Collins McNicholas