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Randstad Quality Engineer in Peabody, Massachusetts

Quality Engineer

job details:

  • location:Peabody, MA

  • salary:$24.93 - $38 per hour

  • date posted:Wednesday, April 7, 2021

  • job type:Contract

  • industry:Professional, Scientific, and Technical Services

  • reference:832496

job description

Quality Engineer

job summary:

A Quality Engineer is needed for a major U.S. defense contractor and industrial corporation with core manufacturing concentrations in weapons and military and commercial electronics in the Peabody, MA area. This job manages low to mid complexity projects determining quality improvement parameters by identifying statistical methods relevant to manufacturing processes. Provides statistical information for establishing quality standards by identifying testing methods and samples.

location: Peabody, Massachusetts

job type: Contract

salary: $24.93 - 38.00 per hour

work hours: 8am to 5pm

education: Bachelors


  • The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs.

  • Provides Quality Engineering support to existing products

  • Supports Quality Control with technical input on inspection documentation and with the Material Review Board (MRB)

  • Reviews product-related change orders, engineering studies and sustaining engineering projects to assure high quality products and adherence to Quality System requirements.

  • Interfaces with Post-Market Quality to review and act upon trended data from complaint investigations and manufacturing metrics.

  • Provides Quality System support to assure compliance with current Medical Device Quality - System Regulation and Medical Device Directive requirements.

  • Reviews/approves specifications, drawings, manufacturing procedures

  • Aids in the development of Inspection Procedures and Test Methods

  • Reviews/approves design verification and validation documentation

  • Supports Risk Management activities

  • Develops Product Quality Plans

  • Coordinates risk assessments and updates Risk Management documentation as required

  • Assists Quality at external manufacturing sites on root cause investigations and corrective actions.


  • Very good working knowledge of medical device Quality System Regulations (21CFR820), ISO 13485 and MDD requirements.

  • Computer literate: able to use word processing, spreadsheet programs, databases.

  • Excellent ability to read, analyze and interpret professional journals, technical procedures and government regulations.

  • Excellent writing skills with ability to write quality assurance reports and detailed procedures.

  • Good presentation skills.

  • Good interpersonal skills to interact with all levels of the company.


  • Bachelor's degree (BA or BS) in a technical discipline. Preferably Manufacturing Engineer or Aerospace Engineering.

  • Minimum of 5 yrs Experience Required



  • Experience level: Experienced

  • Minimum 5 years of experience

  • Education: Bachelors (required)


  • Quality

  • Medical Device

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.