Quality Engineer Intern - Summer 2027

MedlineNorthfield, MN
Onsite

About The Position

A Medline internship provides real-world, hands-on experience where you can make a true impact. Interns take ownership of projects while gaining valuable insight into the day-to-day responsibilities of their roles. Beyond the work itself, the summer experience includes enriching opportunities such as social and networking events, leadership presentations, community service activities, and more. Through meaningful work and professional development experiences, you’ll build a tangible skillset that helps set you apart from your peers. Our internships span a variety of business areas and are open to rising seniors in undergraduate programs. Designed to support both personal and professional growth, the 10-week summer program runs from early June through mid-August in one of our four corporate offices in the Chicagoland area. The Quality Engineer Intern position will entail managing multiple projects related to product quality; i.e. Design Files, Risk Analysis., CAPA process, 510k data collection, product testing, creating documentation for the Master Device Record, etc. We are seeking a dynamic, creative, and hard-working professional looking for hands on experience at a large healthcare company.

Requirements

  • Engineering or Science related majors preferred
  • Junior standing with 3.0 minimum GPA preferred
  • Detail oriented with superior organizational, analytical, and problem-solving skills
  • Motivated self-starter
  • Good documentation skills and an attention to detail
  • Design project experience
  • Unrestricted permanent US work authorization

Responsibilities

  • Developing test plans to evaluate new and existing products
  • Authoring Device Master Records, Design Controls, protocols, reports, and other critical Quality documentation
  • Investigating customer/sales force complaints and assuring files are addressed and closed on time
  • Engaging in process improvement activities related to product quality and regulatory compliance
  • Contributing to product design and development, including generation of documentation required for submission to the FDA
  • Supporting CAPAs, SCARs, supplier maintenance, risk analysis, and more!

Benefits

  • 401(k) contributions
  • paid time off
  • Employee Assistance Program
  • Employee Resource Groups
  • Employee Service Corp
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