Jobs at Medline Industries

Sell medical supplies to physician offices and alternate site customers by building relationships, making daily new calls, presenting products, preparing quotes, maintaining territory plans, training on products, and growing a residual customer base through quota-based, full-cycle outside sales.

Leads complex global regulatory projects for medical devices, including regulatory strategy, product submissions, market approvals, post-market changes, labeling, claims, audits, and responses to regulatory agencies. Evaluates technical evidence against regulations and standards, guides cross-functional teams, manages project timelines, monitors regulatory changes, and supports ongoing compliance. Requires at least four years of medical device regulatory affairs experience and expertise with FDA regulations, 510(k) submissions, and CE Technical Files.