Internship - Manufacturing Engineer

iRhythm Technologies, Inc.FL
110d

About The Position

We are seeking a motivated and detail-oriented Manufacturing Engineer Intern to join our team in a Class II medical device manufacturing facility. This internship provides hands-on experience in production process support, equipment qualification, and continuous improvement within a highly regulated environment. The intern will work closely with manufacturing, quality, and engineering teams to ensure safe, efficient, and compliant production operations. This internship is a 6-month term position with flexible scheduling to accommodate academic commitments, and may be either part-time or full-time.

Requirements

  • Currently pursuing a Bachelor’s or Master’s degree in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering, or related field.
  • Strong problem-solving and analytical skills.
  • Ability to work collaboratively with cross-functional teams.
  • Effective written and verbal communication skills.

Nice To Haves

  • Coursework or experience in lean manufacturing or Six Sigma methodologies.
  • Exposure to regulated manufacturing environments (medical device, aerospace, automotive, etc.).
  • Familiarity with manufacturing equipment, assembly processes, or automation.
  • Experience with CAD software for fixture/tooling design and manufacturing layouts.
  • Proficiency in Microsoft Office; familiarity with data analysis tools (Excel, Minitab, etc.).

Responsibilities

  • Provide day-to-day support for manufacturing operations, including troubleshooting equipment and process issues.
  • Assist with equipment qualification (IQ/OQ/PQ) and process validation activities to ensure compliance with FDA QSR (21 CFR Part 820) and ISO 13485.
  • Participate in continuous improvement projects to improve process efficiency, yield, and quality.
  • Help develop and update standard operating procedures (SOPs), work instructions, and manufacturing documentation.
  • Support new product introduction (NPI) activities, including production line setup and process development.
  • Assist with capacity analysis, workflow optimization, and layout improvements.
  • Collaborate with quality engineering on nonconformance investigations, root cause analysis, and corrective/preventive actions (CAPA).
  • Follow Good Documentation Practices (GDP) and maintain compliance with environmental health and safety (EHS) protocols.
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