Biotech QA Engineer Intern: Design Controls, CAPA & FDA

Medline Industries, Inc. in; Northfield Township (IL); On-site; USD 66,621,000 - 96,708,000; Full time

Job summary

Medline Industries, LP invites applications for the Quality Engineer Intern - Summer 2027 (Biotech). The 10‑week program runs early June through mid‑August in the Chicagoland area, offering hands-on work on product quality, design files, CAPA, 510(k) data, and FDA submission documentation.

You will tackle projects like developing test plans, authoring master records, and driving process improvements while gaining exposure to a large healthcare company.

Qualifications

• Engineering or Science 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 and reports.
• Investigating customer/sales force complaints and ensuring files are addressed on time.
• Engaging in process improvement activities related to product quality and regulatory compliance.
• Contributing to product design and development, including FDA submission documentation.
• Supporting CAPA's, SCAR's, supplier maintenance, risk analysis, and more!

Skills

Detail oriented

Analytical skills

Good documentation

Motivated self-starter

Design project experience

Education

Engineering or Science related majors

Junior standing with 3.0 GPA

Job description

Medline Industries, LP invites applications for the Quality Engineer Intern - Summer 2027 (Biotech). The 10‑week program runs early June through mid‑August in the Chicagoland area, offering hands-on work on product quality, design files, CAPA, 510(k) data, and FDA submission documentation.

You will tackle projects like developing test plans, authoring master records, and driving process improvements while gaining exposure to a large healthcare company.