Medline Industries, LP

Manager, Regulatory Compliance

Medline Industries, LP

full-time

Posted on:

Location Type: Remote

Location: IllinoisUnited States

Visit company website

Explore more

AI Apply
Apply

Salary

💰 $134,000 - $201,000 per year

About the role

  • 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
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
validation processmaster validation planvalidation documentationprocess validation protocolsquality management systems
Soft Skills
leadershipmanagementstrategic development