Quality Operations Director: Strategy, Compliance & Leadership

Medline Industries, Inc. in; Northfield Township (IL); On-site; USD 203,000 - 305,000; Full time

Benefits offered by this job

Competitive compensation

Benefits package

Bonus eligible

Job summary

Medline Industries, LP seeks a Senior Director of Quality Operations (Project Management) to oversee strategic planning for large, complex Quality teams ensuring compliance across pharmaceutical sites. The role leads QA programs, drives CAPA, and ensures readiness for inspections and audits, while aligning with senior leadership to deliver quality and business objectives.

The position requires extensive experience in GMP/ISO environments, strong leadership, and the ability to navigate regulatory

Qualifications

• Bachelor's degree in Engineering, Science, or Technical Field.
• 8+ years in pharma manufacturing with GMP/QSR/ISO.
• 5+ years of management experience.

Responsibilities

• Provide strategic Quality oversight of manufacturing, packaging, testing, and lab operations.
• Ensure product disposition decisions through data evaluation.
• Drive Operational Excellence initiatives focused on quality and continuous improvement.
• Lead and coordinate with Operations, Supply Chain, and Leadership to meet objectives.
• Prepare site for regulatory inspections and audits.
• Oversee QA programs including CAPA, deviations, investigations, and escalation.

Skills

Quality leadership

Regulatory compliance

Risk management

Data analysis

Cross-functional collaboration

Excel proficiency

Education

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

Job description

Medline Industries, LP seeks a Senior Director of Quality Operations (Project Management) to oversee strategic planning for large, complex Quality teams ensuring compliance across pharmaceutical sites. The role leads QA programs, drives CAPA, and ensures readiness for inspections and audits, while aligning with senior leadership to deliver quality and business objectives.

The position requires extensive experience in GMP/ISO environments, strong leadership, and the ability to navigate regulatory