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Medline Industries, LP

Quality Engineer Development Program

Medline Industries, LP

. Provide Quality support throughout the lifetime of products, from design through launch and post-market surveillance .

Posted 10/20/2026full-timeNorthfield • Illinois • United StatesMid-LevelSenior💰 $67,000 - $101,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in Quality Support, including authoring critical documentation and developing test plans while ensuring compliance with regulations. Engages in cross-functional collaboration and process improvement activities to enhance product quality and regulatory adherence.

Highest-signal resume keywords
Quality SupportDevice Master RecordsRisk ManagementProcess ImprovementMS Office Suite

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Quality DocumentationTest Plan DevelopmentRegulatory ComplianceCAPAsSCARsData AnalysisProblem SolvingDetail OrientationProject Management
Soft Skills
CommunicationTime ManagementCollaborationOrganizational Skills
Industry Keywords
Product QualityPost-Market SurveillanceCross-Functional CollaborationCustomer ComplaintsTrend Analysis

About the role

Key responsibilities & impact
  • Provide Quality support throughout the lifetime of products, from design through launch and post-market surveillance
  • Author Device Master Records, Design Controls, Risk Management documents, protocols, reports, and other critical Quality documentation in compliance with applicable regulations
  • Develop test plans to evaluate new and existing products
  • Collaborate with Regulatory, R&D, Product Managers, Manufacturing, Operations, and other cross-functional groups
  • Investigate, track, and trend customer and sales force complaints, including generating trend and Management Review reports
  • Communicate significant issues or developments identified during quality assurance activities and recommend process improvements to management
  • Engage in process improvement activities related to product quality and regulatory compliance
  • Support CAPAs, SCARs, supplier maintenance, and related activities
  • Complete a two-year Quality Engineer Development Program consisting of 12 weeks of High Intensity Training, a 9-month Divisional Corporate Quality rotation, and a 12-month Manufacturing Quality rotation
  • Take ownership of product lines and projects during program rotations
  • Transition into a Quality Engineer-level role upon successful program completion, based on interests and business needs

Requirements

What you’ll need
  • Pursuing a bachelor's degree in science, engineering, or another related major
  • 3.0 minimum GPA preferred
  • Experience processing details, understanding and prioritizing their importance to problem solve, and drawing clear and concise conclusions
  • Experience using time management skills, including prioritizing/organizing, tracking details, and meeting deadlines across multiple projects
  • Experience using MS Office Suite products (Word, Excel, PowerPoint, Outlook)
  • Unrestricted permanent US work authorization

Benefits

Comp & perks
  • Recognition programs
  • Employee resource groups
  • Volunteer opportunities
  • Employee Appreciation Week
  • Competitive healthcare benefits
  • Continuing education and training
  • Health insurance
  • Life and disability insurance
  • 401(k) contributions
  • Paid time off
  • Employee Assistance Program
  • Employee Service Corp
  • Bonus and/or incentive eligibility