This Quality Engineer will be working with a new medical device class 3 implant that is working it's way into commercialization. Clinical Trial results has had great results and the urge to get this product out is a high priority.
- Manual Assembly Validation experience (MOST IMPORTANT)
- Experience creating Batch Records (MOST IMPORTANT)
- Supplier Control and PPAP experience
- Experience with Test Methods and TMV
Sthree US is acting as an Employment Business in relation to this vacancy.