Description
ESSENTIAL DUTIES AND RESPONSIBILITIES:* Participates as a key member of new product development, to help ensure that the new product quality plans, validation plans, specifications, are properly established.
* Executes on process improvements to improve product quality and manufacturability.
* Designs and Develops forms and instructions for recording, evaluating, and reporting quality data
* Interfaces with suppliers to improve or resolve quality issues
* Perform Gauge R&R Studies, IQ, OQ, and PQ Concepts, CAPA compliance.
* Perform Metrology and General Statistics to aid the improvement of processes.
* As part of the Quality team will demonstrate the importance of compliance and quality in all aspects of what they do.
REQUIREMENTS:
* Bachelor's Degree with a scientific emphasis required.
* Minimum of 5 years' experience in a regulated medical device environment.
* ASQ certified Quality Engineer recommended
* Six Sigma Green/Black belt an advantage.
To find out more about Real please visit www.realstaffing.com