Description
Duties- IEC 60601 Medical/electrical equipment safety standards
- Risk management
- Design control
- New product quality plans, validation plans, specifications, are properly established
- Process improvements to improve product quality and manufacturability
- Design and Develop forms and instructions for recording, evaluating, and reporting quality data
- Interface with suppliers to improve or resolve quality issues
- Gauge R&R Studies, IQ, OQ, and PQ Concepts, CAPA compliance
Experience
- Minimum of 5 years' experience in a regulated medical device envirnment
- ASQ certified Quality Engineer recommended
Please be in contact as soon as possible
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