A leading Medical Device company in Orange Country are hiring for a Staff Engineer to lead in the investigation of complex manufacturing product quality and compliance issues. This is an onsite 1-Year contract role in Irvine, CA paying a highly competitive rate with eligibility for overtime as well as access to health/dental/vision/life insurances, and a 401K.
The ideal candidate will meet the following requirements:
- A skilled Engineer with a minimum of 6 years experience in a regulated industry such as Medical Devices
- Experience with injection molding and tool making
- Validation CAD experience
- Project Management experience
- Extensive knowledge and understanding of principles, theories, and concepts relevant to Quality Engineering
- Bachelor's degree in Biomedical or Mechanical Engineering or preferred
If you are available and meet the above requirements, please apply ASAP with your latest resume to be considered.
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