Quality Technician, R&D (Onsite)

Insulet CorporationActon, MA
1dOnsite

About The Position

Position Overview: The Quality Technician is a hands-on, contract role supporting the inspection, documentation, and quality assurance of medical devices during early-stage R&D builds. This position plays a critical role in ensuring product integrity and compliance by performing detailed inspections, maintaining accurate records, and collaborating with cross-functional teams to uphold quality standards throughout the development process. The ideal candidate is detail-oriented, methodical, and committed to maintaining high standards in a fast-paced, collaborative environment. Experience in regulated industries, especially medical devices, is highly valued.

Requirements

  • Strong attention to detail and ability to perform precise inspections under magnification
  • Familiarity with quality control principles and documentation practices in a regulated environment
  • Ability to interpret technical drawings, specifications, and inspection criteria
  • Ability to follow detailed instructions and maintain focus on repetitive tasks
  • Strong communication skills and willingness to ask questions and learn
  • Familiarity with basic computer tools for data entry and documentation
  • Experience working in a regulated manufacturing or R&D environment preferred
  • High School Diploma or GED
  • Minimum 3 years of experience in a quality, manufacturing, or assembly tech/operator role

Nice To Haves

  • Experience in medical device or cleanroom environments is a plus

Responsibilities

  • Conduct in-process and final inspections of small, intricate components and assemblies
  • Review and interpret engineering drawings, specifications, and quality documentation to ensure compliance
  • Record inspection results, deviations, and observations with precision and clarity
  • Maintain accurate and organized documentation in accordance with GMP and ISO 13485 standards
  • Collaborate with engineers to identify and resolve quality issues, and perform root cause analysis and investigation activities
  • Assist in the documenting non-conformances and contributing to root cause analysis and corrective actions
  • Ensure adherence to cleanroom protocols and quality control procedures during all build activities
  • Escalate quality concerns, deviations, and non-conformances
  • Provide input on inspection criteria, documentation practices, and process improvements
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