Quality Engineer Intern: Design, CAPA & FDA Docs

Medline; Northfield Township (IL); On-site; USD 3,168,000 - 4,649,000; Full time

Benefits offered by this job

401(k) contributions

Paid time off

Employee Benefits

Job summary

Medline Industries, LP offers a 10-week summer internship in the Chicagoland area. The Quality Engineer Intern will manage multiple projects related to product quality, design files, CAPA, 510k data collection, product testing, and documentation creation for the Master Device Record.

Open to rising seniors in undergraduate programs. Engineering or Science majors preferred, with a 3.0 GPA, strong organizational and problem-solving skills, and US work authorization.

Qualifications

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

Responsibilities

• Managing multiple projects related to product quality (Design Files, Risk Analysis, CAPA).
• Creating documentation for the Master Device Record and FDA submissions.
• Developing test plans to evaluate products.
• Engaging in process improvement related to product quality and regulatory compliance.

Education

Engineering or Science related majors preferred

Junior standing with 3.0 minimum GPA

Unrestricted permanent US work authorization

Job description

Medline Industries, LP offers a 10-week summer internship in the Chicagoland area. The Quality Engineer Intern will manage multiple projects related to product quality, design files, CAPA, 510k data collection, product testing, and documentation creation for the Master Device Record.

Open to rising seniors in undergraduate programs. Engineering or Science majors preferred, with a 3.0 GPA, strong organizational and problem-solving skills, and US work authorization.