Manager, Regulatory Compliance

Role Overview

• Responsible for leading the management of master validation program and compliance maintenance
• Support senior management in development of validations process, master validation plan, and strategies
• Manage the Compliance Master Validations team
• Develop and Manage Medline’s supplier master validation plans and validation documentation

Requirements

• Bachelor’s degree in engineering, chemistry, biology, or related sciences
• At least 4 years of experience with medical device or pharma, QA and/or Quality Management Systems including validations
• Experience authorizing medical device process validation protocols and reports

Benefits

• Health insurance
• Life and disability
• 401(k) contributions
• Paid time off