Risk Management Engineer

Job not on LinkedIn

🕒 April 29

🌽 Illinois – Remote

🌽 Illinois – Remote

💵 $79k - $119k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔒 Insurance

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Medline Industries, LP

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1910

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

💰 Private Equity Round on 2021-06

Healthcare • Logistics • Manufacturing

Medline Industries, LP is a leading healthcare company that focuses on improving clinical, financial, and operational outcomes for its customers. The company offers a wide array of over 335,000 medical products and boasts extensive warehousing capabilities with more than 28 million square feet of space. With a significant global presence of 43,000 employees, Medline provides agile and scalable solutions across all points of care, achieving a 95% next-day delivery rate within the US. The company's mission is to enhance healthcare delivery by providing superior products, supply chain resilience, and clinical expertise, all while fostering strong customer relationships through tailored, problem-solving solutions.

📋 Description

• Key contributor within the organization that monitors, maintains, and enhances risk controls by analyzing quality data and major quality events • Responsible for managing an automated risk-based trending system • Provide expertise to the organization including education, technical support, issue resolution, and integration of new or enhanced risk controls • Collaborate with Medline’s R&D team during design and development • Work with Subject Matter Experts (SMEs) to create a framework for Risk-based dashboards • Analyze and normalize multiple streams of data to gauge the health of the risk management system • Proactively work with members of the division or project team to identify issues that might delay the project • Develop timelines for all projects and ensure that deadlines and goals are being met • Take action to address identified inefficiencies in Medline’s global quality management system.

🎯 Requirements

• Bachelor of Science Degree in Biology, Chemistry, Engineering or Statistics-based degree • At least 2 years of QA/QE experience in a cGMP Device or environment • Complete device life cycle experience related to design, production, use of a device, and ISO 14971 • Experience with Data visualization tools/business intelligence tools such as Tableau, Power BI, or Qlik • Experience leading multiple, complex projects • Strong ability to manage multiple priorities • Self-starter attitude • Good oral and writing skills • Ability to work independently and as a team in an efficient manner.

🏖️ Benefits

• Health insurance • Life and disability insurance • 401(k) contributions • Paid time off • Employee Assistance Program • Employee Resource Groups • Employee Service Corp