May 19, 2021
The purpose of this position is to assume primary responsibility for the ISO 13485 registration and maintenance of the Nectar PD organization. The Medical Quality Engineer is responsible for ensuring the product development service and support activities of medical devices produced meet the requirements of 21 CFR Part 820, ISO 13485, the Medical Device Directive and other applicable regulations and standards. This position supports the operations team (design & engineering) through all phases of our medical products lifecycle. In addition, involvement with the internal audit process is required. This is a part time position.
Nectar Product Development E Regal Ct, Tulsa, OK 74133, USA Full time