Senior Quality Engineer

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  • As an Equal Employment Opportunity Employer, DAVIS has reporting requirements which require us to invite employees to voluntarily self-identify their race/ethnicity. Submission of this information is voluntary and refusal to provided it will not subject you to any adverse treatment. The information obtained will be kept confidential.
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Senior Quality Engineer

  • Specialty:

    Engineering
  • Title:

    Senior Quality Engineer
    • City:

      Ashland
    • State:

      MA
    • Zip Code:

      01721
  • Start date:

    06-26-2017
  • Status:

    Closed
  • Assignment Type:

    Direct Hire
  • Job Id:

    42701

Description

Our client located in Ashland, MA is looking for a Senior Quality Engineer to join their team on a direct hire basis. 

 

Responsibilities of the Quality Engineer

  • This position is responsible for providing quality engineering support to operations and product development engineering to investigate, plan, and implementing product quality improvements in and/or additions to current products and manufacturing processes that directly affect safety, quality, regulatory compliance, and/or productivity. 
  • In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. 
  • Provide technical assistance to plan and implement specified projects to be completed including organizing and leading projects of various departments, planning and scheduling, coordinating resources (personnel, materials, time, money, suppliers), preparing proper documentation, etc. 
  • Lead cause-identification and problem-resolution for various types of quality, production or service-related issues. 
  • Provide quality engineering input in the design, fabrication, development, installation, validation, and qualification of equipment / processes which may include feasibility studies and/or proper documentation for justification of project and training. 
  • Plan and implementation of quality related projects to develop, install, and qualify new processes for manufacturing new products or improving existing processes. 
  • May assist in maintaining plant-wide calibration system and drawing control/document control system. 
  • Gather, track, and analyze production data for meetings, business plan, etc. (yields/output/efficiencies). 
  • Plan work schedules, expenditures, attend meetings, and prepare monthly reports as required. 

 

Qualifications of the Quality Engineer

  • Requires a four-year college degree in an engineering, scientific, or technical discipline with a minimum of three years of experience in a Quality Engineering or Process Engineering role in a regulated environment. 
  • In lieu of a four year degree, a high school diploma or equivalent and nine years of quality engineering experience in a regulated manufacturing environment 
  • Basic computer software skills, i.e. Microsoft Office. Experience in medical device or pharmaceutical industry preferred.

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