Jobs at Medline Industries

Sell medical supplies and diagnostics to physician offices and alternate site customers. Build territory, cold-call daily, present products, prepare quotes, train on product benefits, and grow a residual customer base while maintaining territory plans and relationships.

Lead multi-shift manufacturing and production operations for a high-SKU medical device reprocessing facility. Drive throughput, compliance with FDA and quality standards, training, continuous improvement, automation and capital projects, cross-functional collaboration, performance metrics, and site leadership including customer visits and facility tours.

Provide product and sales teams with product support: resolve customer/sales inquiries, research and cross-reference external brands to Medline products, report issues and training gaps, coordinate vendor/item setup, and provide administrative support to sales reps.

Process accounts payable transactions, reconcile vendor statements, research and resolve discrepancies, maintain aging/GR-IR/parked reports, prepare monthly portfolio scrubs, ensure proper approvals, communicate with vendors/internal stakeholders (via Zendesk), and support ad hoc AP projects.

Analyze workforce, facility layout, and operational data; perform time studies, value stream mapping, process capability and statistical analysis; support and implement Lean, Six Sigma, Kaizen and 5S initiatives; recommend efficiency improvements; train personnel and run Kaizen events; administer continuous improvement programs.

Lead planning, execution, and reporting of statistical analyses for clinical and outcomes research. Develop SAPs, sample size calculations, and randomization schedules; analyze and interpret data using SAS and power-analysis tools; ensure data integrity and Part 11 compliance; mentor staff and contribute to Clinical Study Reports.

Lead planning and execution of global regulatory projects to obtain and maintain device approvals. Develop regulatory strategies for new devices, markets, and post-market changes; prepare and submit filings (e.g., 510(k), CE Technical Files); respond to regulators; manage cross-functional teams; support labeling, audits, compliance tracking, and process improvements. Travel up to 10%.