Position : Biomedical Engineer II / Quality Engineer II , Req# : 8007-1
Location : Irvine, CA (100% onsite)
Duration : 12+ Months Contract
Job Description :
What does this group do? New Product Development; Quality function for the development of new products.
Specific technology / software used? SolidWorks, Risk Management, Clean-Room Build Support
What will a typical workday look like? Oversee design verification and validation builds, perform data analysis, develop inspection procedures, validate inspection procedures, write process validation protocols, write process validation reports.
Support CMO transfer activities.
What will the work schedule be? 8 am-5 pm; No overtime. Occasionally may get OT during peak project periods.
Will there be any travel involved? No. Occasionally may be needed at CMO if there’s an urgent need
What are your top 3 required technical skills? Must haves? Test method development, the device builds in cleanroom and risk management.
Nice to have skills? New product development experience, receiving inspection, design verification
Education and Experience :
- Bachelor's degree in engineering required.
- 2-4 years of experience required.
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