Quality & Compliance Director, Medical Devices

Medline

Waukegan (IL)

On-site

USD 154,000 - 231,000

Full time

14 days+

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Benefits offered by this job

Health insurance
Life insurance
Disability insurance
401(k) contributions
Paid time off

Job summary

Medline is seeking a Senior Quality Leader in Illinois to drive strategy, oversee multiple QA departments, and ensure compliant, high-quality Medline-branded products. You will coordinate with executives, suppliers, and manufacturing partners to deliver on-time, safe products.

The role requires 7+ years in regulated medical device or related fields, strong data analysis, and advanced Excel skills. Travel up to 30% is expected, with a competitive salary package and bonus eligibility.

Qualifications

  • Bachelor’s degree in Engineering, Science, or Technical Field required.
  • At least 7 years of experience in design/operation of medical device or drug combination product platforms or regulated industries.
  • Strong data analysis and reporting skills; proficient in Excel and related tools.

Responsibilities

  • Direct the development of product specifications for Medline branded products, testing, inspection, and qualification.
  • Partner with Supplier Audit and Division to optimize supplier relationships and quality programs.
  • Develop and implement QA strategy and lead quarterly management reviews and customer presentations.
  • Ensure compliance with QSR/GMP/ISO requirements through audits and continuous improvement.
  • Oversee multiple departments, manage budgets, policies, and staffing to support strategic goals.

Skills

Leadership
Data analysis
Project management

Education

Bachelor’s degree in Engineering, Science, or Technical Field

Tools

Microsoft Excel

Job description

Medline is seeking a Senior Quality Leader in Illinois to drive strategy, oversee multiple QA departments, and ensure compliant, high-quality Medline-branded products. You will coordinate with executives, suppliers, and manufacturing partners to deliver on-time, safe products.

The role requires 7+ years in regulated medical device or related fields, strong data analysis, and advanced Excel skills. Travel up to 30% is expected, with a competitive salary package and bonus eligibility.

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