Senior Quality Manager

About Our Client

This is a global, well-capitalized manufacturer operating in regulated life science markets with significant recent investment in U.S. operations. The site is modern, growing, and highly visible within the broader organization, offering strong influence and long-term opportunity.

• Own and execute site-wide quality strategy across QA, QC, QMS, and supplier quality
• Lead and develop a multi-layered quality organization with direct reports across functions
• Ensure compliance with ISO 13485 and applicable regulatory requirements
• Act as the senior quality representative for customer, supplier, and regulatory audits
• Drive CAPA, nonconformance management, change control, and risk management
• Partner with site leadership to embed a right-first-time, continuous improvement culture

MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.

MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.

The Successful Applicant

A successful Senior Quality Manager should have:

• Bachelor's degree in Engineering or a scientific discipline
• Proven experience as a site-level Quality Manager in regulated manufacturing
• 5-10+ years of people management experience
• Strong working knowledge of ISO 13485
• Background in medical device manufacturing (required)
• Experience in cleanroom or assembly-based manufacturing environments

• A competitive salary ranging from $165,000 to $175,000, based on experience.
• True site ownership with authority to shape quality strategy
• Leadership role in a newly built, state-of-the-art manufacturing facility
• Large, experienced quality team with strong cross-functional visibility
• Backing of a stable, global organization with long-term growth plans

If you are ready to take the next step in your career as a Senior Quality Manager, apply now to join an industry-leading team.