1970-01-01Davis Companieshttp://www.daviscos.com/wp-content/themes/davis_theme/assets/images/logo.svg325 Donald J. Lynch Boulevard, Suite 201MarlboroughMA01752USAcustomer support[+800-482-9494][+508-481-8519]

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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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Medical Device Assembler

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  • Title:

    Medical Device Assembler
    • City:

      Brooklyn Park
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DAVIS Companies has partnered with a leader in Medical Device manufacturing to identify an Assembler to join their team! This is a 1st shift position, working 6AM-2:30PM.

Qualifications of the Medical Assembler:

  • High school diploma or equivalent required
  • Must have 2 to 3 years of previous medical device assembly experience.
  • Must be able to understand verbal and written work instructions.
  • Basic mathematical skills as required to perform job duties (add, subtract, multiply, divide).
  • Must be able to work in a clean room environment and follow the clean room environment practices and procedures.
  • Must be able to perform repetitive work according to set procedures, sequence and pace.
  • Knowledge of GDP, GMP, and Lean Manufacturing preferred.
  • Maintains confidentiality of documents and processes.
  • Must have fine motor skills and high degree of dexterity and eye coordination to work with and assemble small parts and subassemblies using both hands.
  • Must be able to operate manufacturing and measurement equipment such as microscopes, test equipment, EFDs, ultrasonic welders, soldering irons, dial calipers, pressure gages, and rulers.

Responsibilities of the Medical Assembler:

  • Experienced in assembling medical devices on two or more product lines at or above the quantity standard rate projected by the supervisor or lead.
  • Demonstrates an understanding of our Quality System Policies by referencing and explaining written line procedures.
  • Complete and maintain accurate written records of manufacturing operations on production documentation following appropriate training i.e. Device History Records, Data Sheets and Lot Control.
  • Adaptable to changes in procedures and is able to learn new procedures due to product line and technology modifications.
  • May be asked to cross train on a variety of product line operations.
  • May assist Assembler III or Lead in training procedures.
  • General understanding of LEAN Manufacturing Principals to assist in improving established metrics.
  • Proactively informs the lead or supervisor of material shortages.
  • Maintains a safe work environment by following and practicing good housekeeping and safety guidelines policies
  • Maintain acceptable standards for attendance and work overtime and varying shifts as needed. 

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