Quality Engineer I - Medical Devices – Fremont

To develop and implement appropriate quality system elements to ensure the high quality level of new and existing products. Follows standards and procedures in analyzing situations or data from which conclusions can be readily obtained.

Key Responsibilities

• Participate in the development and qualification activities related to the derivative B products. *
  
• Develops testing and inspection methodology and documentation for new and existing products *
  
• Designs and installs QC process sampling systems, procedures, and statistical techniques *
  
• Designs or specifies inspection and testing mechanisms and equipment *
  
• Performs failure analyses and defect investigations *
  
• Analyzes production limitations and standards *
  
• Recommends revision of specifications *
  
• Interfaces with other engineering departments within the company, customers, and suppliers on quality related issues *
  * Indicates Essential Function
  
  Quality Systems Duties and Responsibilities
  
  Fully support the Quality Policy by building quality into all aspects of the incumbent's work and by maintaining compliance to all quality requirements (including but not limited to being current on all training requirements for the incumbent's position and documenting that training).
  
  Qualifications
  
  0-3 Years experience with BA/BS or equivalent in Quality Engineering or related discipline. Strong written/verbal communication skills. Demonstrated used of Quality tools/methodologies.
  
  Apply Here