Jobs at Medline Industries

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.

No job responsibilities or requirements provided. Posting contains only an equal opportunity employer statement and "NA" as the job description.

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%.