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Manufacturing Engineer

  • Specialty:

  • Title:

    Manufacturing Engineer
    • City:

      Ham Lake
    • State:

    • Zip Code:

  • Start date:

  • Status:

  • Assignment Type:

    Contract To Hire
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DAVIS Companies has partnered with a leader in Medical Device and Pharma manufacturing, to identify a Manufacturing Engineer to join their team! This individual must be located in MN. 


  • Assist in the development and qualification of Medical Device and Industrial productions
  •  Write detailed production documentation
  •  Evaluate manufacturing processes by designing and conducting research programs; applying knowledge of product design, fabrication, assembly, tooling, and materials; conferring with equipment vendors; soliciting observations from operators.
  •  Develop manufacturing processes by studying product requirements; researching, designing, modifying, and testing manufacturing methods and equipment
  •  Improve manufacturing efficiency by analyzing and planning work flow, space requirements, and equipment layout.
  • Assure product and process quality by designing testing methods; testing finished goods, determining product and process capabilities; establishing standards; confirming manufacturing processes.
  • Provide manufacturing decision-making information by calculating production, labor, and material costs; reviewing production schedules; estimating future requirements.
  • Prepare product and process reports by collecting, analyzing, and summarizing information and trends
  • Maintain product and company reputation by complying with FDA, ISO9001 and ISO13485 regulations.
  • Maintain a commitment to vision and “spirit” by partnering with new and current employees by demonstrating outstanding service and integrity.  


  • Minimum of Bachelors Degree in Manufacturing Engineering OR other relevant Engineering discipline.
  • At least 3 years of pharma or medical experience.
  • Robust understanding of process validation concepts and practices including, IQ, DOE, OQ, PQ and PPQ
  • Basic understanding of ISO Quality System requirements and FDA regulations
  • Adept and experienced problem solver able to determine root cause of technical issues and implement effective solutions in a timely manner




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