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Part-Time QC Inspector

Under little supervision the QC Inspector will be responsible for inspecting and packaging products or raw material using inspection tools and methodologies. When a nonconformance is found, they may initiate nonconforming material reports and assist in the process.

Work hours:

  • Monday – Friday: 8:00AM-2:00PM or 10:30AM-4:30PM

Specific duties & responsibilities

  • Perform product or raw material inspection using microscope, pin gage, caliper, ruler, laser micrometer, and other tools or methods and properly label and segregate non-conformance products from acceptable ones.
  • Review travelers to ensure good documentation practices are performed by operators.
  • Initiate nonconforming material reports (NMR) for products or raw material found to be out of specification, investigate non-conformance for root cause, and help implement solutions to improve non-conformance.
  • Work with the production team to communicate the importance of quality and following procedures.
  • May provide recommendations and participate in continuous improvement projects.
  • Act as eyes and ears of the Quality department to promote and communicate GMP and GDP.
  • Support QC Leads and Engineering Projects as needed
  • Other duties as assigned.

Experience & education requirements

  • High school diploma or GED or related work experience and/or training.
  • 0-3 years of medical device experience with at least 6 months in a quality role preferred.
  • Must exhibit a willingness to work on teams and promote teamwork among other employees.
  • Highly focused, detailed oriented, and has excellent eyes for spotting product or material nonconformity.
  • Proficient in reading, writing, and speaking English
  • Physical Requirements: Must be able to work with a microscope, rulers, micrometer and sit for an extended period of time.
Location: Roseville, MN
Employment Type: Part-time
Minimum Experience: 0 years

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About VitalPath

VitalPath is the new name for the merging of VitalDyne Medical & Catheter and Medical Design. We’re ISO 13485:2016 certified and FDA registered.