Quality Engineer, 2-Year Development Program

Medline Industries, LP

United States

On-site

USD 67,000 - 101,000

Full time

14 days+

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Job summary

Medline Industries, LP is launching a two-year Quality Engineer Development Program designed to build a strong quality foundation. The program begins with 12 weeks of High Intensity Training (HIT), followed by 9 months in Divisional Corporate Quality and 12 months in Manufacturing Quality at domestic sites.

Participants will own product quality projects, develop in design controls and CAPA processes, and work with Regulatory, R&D, and Manufacturing teams to drive improvements.

Qualifications

  • Pursuing a bachelor's degree in science, engineering, or related major with a 3.0 GPA minimum preferred.
  • Experience prioritizing and meeting deadlines across multiple projects.
  • U.S. work authorization is required.

Responsibilities

  • Provide quality support across product lifecycle from design to post-market.
  • Author Master Records, Design Controls, Risk Management, and related docs per regs.
  • Develop test plans for new and existing products.
  • Collaborate with Regulatory, R&D, Product Managers, Manufacturing, Ops.
  • Investigate and trend customer and sales force complaints; generate reports.
  • Communicate significant QA issues and propose process improvements.
  • Engage in processes improving product quality and regulatory compliance.
  • Support CAPAs, SCARs, supplier maintenance, and more.

Skills

Attention to detail
Time management
Problem solving
Documentation

Education

Bachelor's degree in science or engineering (pursuing)

Tools

MS Office

Job description

Medline Industries, LP is launching a two-year Quality Engineer Development Program designed to build a strong quality foundation. The program begins with 12 weeks of High Intensity Training (HIT), followed by 9 months in Divisional Corporate Quality and 12 months in Manufacturing Quality at domestic sites.

Participants will own product quality projects, develop in design controls and CAPA processes, and work with Regulatory, R&D, and Manufacturing teams to drive improvements.

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