Quality Engineer Development Program - Summer 2027 Start

Medline Industries, LP•Northfield, IL
•$67,000 - $101,000

About The Position

The Quality Engineer Development Program is a two-year early-career program designed to build the knowledge, tools, and experience needed to become a successful Quality Engineer at Medline. It begins with 12 weeks of High Intensity Training, including eLearnings, instructor-led trainings, and real-world assignments. Participants then complete a nine-month Divisional Corporate Quality rotation and a 12-month Manufacturing Quality rotation at a domestic manufacturing site. During the rotations, participants take ownership of product lines and projects that reinforce and challenge what they learned during training. After successfully completing the program, employees may move into a Quality Engineer-level role suited to their interests and Medline’s business needs. The role provides Quality support throughout a product’s lifecycle, from design and launch through post-market surveillance. It involves preparing critical Quality documentation, developing product test plans, collaborating with cross-functional teams, analyzing customer and sales force complaints, communicating significant quality issues, recommending process improvements, and supporting quality and regulatory initiatives.

Requirements

  • Pursuing a bachelor's degree in science, engineering, or another related major.
  • Unrestricted permanent US work authorization.
  • Experience processing details, understanding and prioritizing their importance, and using them to solve problems and draw clear, concise conclusions.
  • Experience using time-management skills to prioritize and organize work, track details, and meet deadlines across multiple projects with varying completion dates.
  • Experience using MS Office Suite products, including Word, Excel, PowerPoint, and Outlook.

Nice To Haves

  • Minimum 3.0 GPA preferred.

Responsibilities

  • Provide Quality support throughout the product lifecycle, from design and launch through post-market surveillance.
  • Author Device Master Records, Design Controls, Risk Management documentation, protocols, reports, and other critical Quality documentation in compliance with applicable regulations.
  • Develop test plans to evaluate new and existing products.
  • Collaborate with Regulatory, R&D, Product Managers, Manufacturing, Operations, and other cross-functional groups.
  • Investigate, track, and trend customer and sales force complaints, including generating trend and Management Review reports.
  • Communicate significant issues or developments identified during quality assurance activities and recommend process improvements to management.
  • Engage in process improvement activities related to product quality and regulatory compliance.
  • Support CAPAs, SCARs, supplier maintenance, and related activities.
  • Take ownership of product lines and projects during the program rotations.

Benefits

  • Competitive healthcare benefits
  • Health insurance
  • Life and disability insurance
  • 401(k) contributions
  • Paid time off
  • Continuing education and training
  • Recognition programs
  • Employee resource groups
  • Volunteer opportunities
  • Employee Appreciation Week
  • Access to the Employee Assistance Program and Employee Service Corp for employees working less than 30 hours per week
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service