About the role#
This is a full-time, paid internship for the Summer of 2027. You will work on-site at our Northfield or Chicago locations. The program runs for 10 weeks from early June through mid-August. You will take ownership of projects related to product quality, including design files, risk analysis, and the CAPA process.
What you'll do#
- Develop test plans to evaluate new and existing products.
- Author Device Master Records, design controls, protocols, and reports.
- Investigate complaints from customers and the sales force.
- Engage in process improvement activities regarding regulatory compliance and product quality.
- Support CAPAs, SCARs, supplier maintenance, and risk analysis.
- Contribute to product design and development by generating documentation for FDA submissions.
What you'll need#
- Current enrollment in a degree program for Biomedical, Mechanical, or Industrial Engineering, or Biomedical Sciences, Chemistry, or Physics.
- Junior standing with a minimum 3.0 GPA is preferred.
- Unrestricted permanent US work authorization.
- Strong organizational, analytical, and problem-solving skills.
- Experience with design projects.
- Attention to detail and documentation skills.
Location & details#
- Locations: Northfield, Illinois and Chicago, Illinois.
- Work Modality: On-site.
- Term: Summer 2027.
About Medline Industries, LP
Medline Industries, LP manufactures and distributes medical-surgical products. The company provides supply chain solutions to healthcare providers across various care settings. It operates in more than 100 countries and maintains a global workforce of over 45,000 people. The corporate headquarters are located in Northfield, Illinois.
How to get in at Medline Industries, LP
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