Quality Engineer Intern - Hands-on QA & Regulatory Docs

Medline Industries, LP

Chicago (IL)

On-site

USD 32,000 - 47,000

Full time

6 days ago

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Benefits offered by this job

401(k) contributions

Paid time off

Employee Assistance Program

Employee Resource Groups

Intern Service Corp

Job summary

Medline Industries, LP invites you to join our 10-week Quality Engineer Intern program in the Chicagoland area. Interns will own projects tied to product quality, including Design Files, risk analysis, CAPA processes, and FDA data collection, while gaining hands-on experience at a large healthcare company.

The internship runs from early June through mid-August across four corporate offices in the Chicago area, offering social/networking events, leadership presentations, and professional

Qualifications

Engineering or Science majors preferred.
Junior standing with 3.0 minimum GPA preferred.
Detail oriented with strong organizational, analytical, and problem-solving skills.
Motivated self-starter with good documentation skills.

Responsibilities

Manage multiple projects related to product quality (Design Files, Risk Analysis, CAPA).
Create documentation for Master Device Record and FDA submissions.
Support quality processes, data collection, and testing activities.
Contribute to design controls and development documentation.

Skills

Detail oriented

Analytical

Problem solving

Organizational

Self-starter

Documentation

Design project experience

Education

Engineering or Science majors preferred

Junior standing with 3.0 GPA preferred

Job description

The internship runs from early June through mid-August across four corporate offices in the Chicago area, offering social/networking events, leadership presentations, and professional

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