Supplier Management Engineer

Job not on LinkedIn

🕒 April 28

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Logo of Medline Industries, LP

Medline Industries, LP

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

• Conduct supplier audits to verify compliance with ISO 9001, ISO 13485, and applicable regulatory requirements related to high-risk vendors • Support supplier qualification, requalification, and disqualification activities for moderate to high-risk suppliers, including documentation review and approval routing • Review and approve supplier quality records and compliance documentation in accordance with internal procedures • Execute Supplier Corrective Action Requests (SCARs) by tracking actions, verifying evidence, and documenting effectiveness under supervision • Assist with supplier communication related to quality requirements, documentation requests, and corrective actions to Medline’s internal business partners and external suppliers • Provide technical guidance and training to suppliers on quality standards and best practices • Support containment activities and investigations related to supplier nonconformances • Utilize root cause analysis and risk management tools to prevent recurrence of issues • Maintain accurate and timely records of supplier audits, performance reviews, nonconformances, and corrective actions • Prepare routine reports, dashboards, and summaries for supplier quality performance and compliance tracking

🎯 Requirements

• Bachelor’s degree in Engineering, Biology, Quality Management, or related field • 3–5 years in supplier quality, manufacturing quality, or similar role • Knowledge of ISO standards, FDA regulations (if applicable), statistical process control (SPC), and quality tools (FMEA, PPAP, APQP) • Strong communication, problem-solving, and negotiation skills • Medical Device or drug experience • Travel up to 25% (domestic and/or international)

🏖️ Benefits

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

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