Quality Assurance Inspector

GentuitySudbury, MA

About The Position

The Quality Assurance Inspector will perform inspections of incoming materials, components, and subassemblies. This role also includes completing First Article Inspections, performing in-process and finished product inspections and testing (both sterile and non-sterile, disposable, and durable), and conducting DHR reviews for subassemblies and finished goods. The inspector will also be responsible for product release activities for all conforming products, initiating NCR records for non-conforming items, quarantining non-conforming product, and participating in the investigation process. Additionally, the role involves maintaining inspection area equipment calibration and PM, adhering to and promoting GMP and GDP principles, and assisting in external/internal audit preparations.

Requirements

  • Organizational skills and attention to detail.
  • Firsthand experience using measuring tools such as but no limited to calipers, micrometers, pin gauges and tensile testers.
  • Ability to read and understand drawings.
  • Experience working with sampling plan.
  • Understanding of ISO 13485, CFR21-820, ISO 146444-1, 2 and 3.
  • Able to take direction, ownership, and responsibility for QMS related activities.
  • Positive and cooperative communication and collaboration with all levels to employees, contractors and vendors.
  • Strong understanding of quality control standards and testing techniques.
  • Electronic Quality System experience.
  • Proficient with Microsoft Office, Excel, and other electronic systems.

Nice To Haves

  • Medical device experience is a plus.
  • Experience working a cleanroom is a plus.

Responsibilities

  • Perform inspection of incoming materials, components, and subassemblies.
  • Complete First Article Inspections upon request.
  • Perform In-process and finished (sterile and non-sterile, disposable, and durable) product inspection and testing.
  • Perform DHR reviews for subassemblies and finished goods.
  • Conduct Product Release activities for all conforming products.
  • Initiate NCR records for all non-conforming products, components, and subassemblies.
  • Quarantine non-conforming product and participate in the investigation process.
  • Maintain Inspection area equipment calibration and PM.
  • Adhere and promote GMP and GDP principles.
  • Assist in external/internal audit preparations.
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