Senior Engineer, Supplier Management

Job not on LinkedIn

🕒 April 28

🌽 Illinois – Remote

🌽 Illinois – Remote

💵 $101k - $152k / year

⏰ Full Time

🟠 Senior

👷🏻‍♀️ Engineer

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Medline Industries, LP

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1910

⚕️ Healthcare Insurance

💊 Pharmaceuticals

💰 Private Equity Round on 2021-06

Healthcare Insurance • Pharmaceuticals

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

• Lead Medline’s supplier quality oversight for a global supply base • Own risk‑based qualification, performance management, scorecards, and audit execution for high‑risk suppliers • Drive cross‑functional corrective and preventive actions and supplier development to improve quality, reliability, and compliance • Lead risk‑based supplier oversight across regions; set audit/monitoring depth by risk tier and product classification • Lead communication efforts related to high-risk suppliers with internal stakeholders • Own complex supplier qualifications and disqualifications for critical suppliers, including technical documentation reviews and potential on‑site assessments • Author and maintain supplier quality agreements and inspection plans with Procurement/Legal; ensure alignment with device regulations and regional requirements • Analyze trends and drive SCAR/CAPA to effectiveness verification; escalate per governance • Work with quality support groups to proactively identify issues and lead the containment of them • Provide technical guidance and training to suppliers on quality standards and best practices • Troubleshoot in-depth vendor issues that impact multiple business units to improve the global supply chain and improve supplier processes • Mentor Quality Engineers/QEDP associates and coach divisional QA on supplier controls, SCAR quality, and problem‑solving methods • Maintain accurate records of audits, performance reviews, and compliance reports • Assist or perform audits associated with high-risk suppliers to ISO 13485, ISO 9001, and/or and applicable regulatory requirements

🎯 Requirements

• Bachelor’s degree in Engineering, Biology, Quality Management, or related field • 6-8 years in supplier quality, manufacturing quality, or similar role • in-depth knowledge of ISO standards and FDA regulations • strong communication, problem-solving, and negotiation skills • ownership of CAPA or SCAR throughout its lifecycle • strong Medical Device or Drug regulatory experience • strong critical thinking abilities • experience with statistical process control (SPC), and quality tools (FMEA, PPAP, APQP)

🏖️ Benefits

• health insurance • life and disability • 401(k) contributions • paid time off • access to the Employee Assistance Program • Employee Resource Groups • Employee Service Corp