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Quality Engineer 2 - Medical Device
The Quality Engineer II is responsible for developing the full reliability and inspection plan for all new products.  This person evaluates products, manufacturing processes, assembly processes, and supports quality control activities through training, inspection procedure preparation, and technical support. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Coordinates design review meetings to review all quality aspects of new products.  Interfaces with Product Development Engineers to ensure quality considerations during the concept stage. Develops various inspection techniques and procedures to ensure product integrity to design specifications.  Responsible for the writing, approval and implementation of Incoming,


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