3-Month contract, with high possibility of permanent conversion.
On-site, 5 days per week.
Qualifications
BS in a relevant scientific or engineering discipline, with 7+ years in the medical device field.
The ideal candidate should have hands-on experience in risk identification, design verification, and testing.
Full understanding of the design control process, and ISO 13485 & EU-MDR.
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Sr Quality Engineer • Irvine, CA, United States
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