Global Director of Quality Engineering

Owens & Minor; Alpharetta (GA); On-site; USD 170,000 - 190,000; Full time

Benefits offered by this job

Comprehensive Healthcare Plan

Educational Assistance

Employer-Paid Life Insurance

Voluntary Supplemental Programs

Adoption assistance

HSA and 401(k)

Paid Leave

Well-Being programs

Job summary

Owens & Minor is seeking a Director of Quality Engineering to provide global leadership across product development, manufacturing, distribution, supplier quality, and post-market activities. The role develops Quality Engineering strategies, standards, and capabilities to ensure medical devices are designed, manufactured, and distributed in compliance with safety and regulatory requirements.

The Director leads a high-performing Quality Engineering organization, embedding prevention-based

Qualifications

• Bachelor’s degree in engineering, science, statistics, quality, or a related technical discipline required.
• 5+ years of progressive leadership experience in Quality Engineering.

Responsibilities

• Develops and executes the global Quality Engineering strategy in alignment with QA strategy and business needs.
• Leads Quality Engineering professionals across manufacturing facilities and distribution operations.
• Establishes standards, governance, processes, tools, and performance expectations across the product lifecycle.
• Provides technical Quality leadership for development, manufacturing, distribution, and post-market activities.
• Embeds prevention-based Quality Engineering practices into early product development and manufacturing processes.
• Drives continuous improvement using data, statistics, and cost-of-quality measures.

Skills

Quality engineering

Leadership

Regulatory knowledge

Statistical methods

Education

Bachelor’s degree in engineering/ science/ quality

Master’s degree preferred

Job description

Owens & Minor is seeking a Director of Quality Engineering to provide global leadership across product development, manufacturing, distribution, supplier quality, and post-market activities. The role develops Quality Engineering strategies, standards, and capabilities to ensure medical devices are designed, manufactured, and distributed in compliance with safety and regulatory requirements.

The Director leads a high-performing Quality Engineering organization, embedding prevention-based