Principal Quality Engineer
My class III device client located in Irvine who is looking to bring on a full-time Principal Quality Engineer in hopes that you will move into a Quality Manager opening.
This position is located in the heart of Irvine- the company pays VERY competitively, has stock & bonus included in their overall offer letters along with full benefits.
Please see below for a few details regarding the role:
-Ideally, you will have 8+ years of experience within medical device class III implantable experience
-Strong understanding of 21 CFR 820, 13485, and 14971
-Must have engineering degree
-Strong knowledge of statistics and experience in device development and manufacturing environments
-Responsible for product development and design control - process development, risk mgmt., TMV etc.
My client will provide relocation if needed.
Sthree US is acting as an Employment Agency in relation to this vacancy.