Global Director, QMS

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🇺🇸 United States – Remote

⏰ Full Time

🔴 Lead

👔 Director

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Neogen Corporation

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Neogen®’s Solutions Can Be Found at Every Step of the Food Chain.

📋 Description

• Define, lead, and govern the global QMS operating model, including enterprise-wide standards, processes, governance mechanisms, decision rights, and deployment expectations across Global, Regional, and Site Quality organizations. • Drive global QMS strategy, harmonization, and modernization initiatives, including simplification, digital enablement, standardization, scalability, and integration to support growth and acquisitions. • Ensure QMS processes, procedures, documentation, and execution remain aligned with applicable regulatory requirements, industry standards, audit expectations, and business objectives. • Provide enterprise oversight for key QMS processes, including CAPA, change control, document control, deviation management, risk management, training, and quality performance metrics. • Lead systemic audit readiness and support regulatory inspections, third-party audits, and internal audits through robust global QMS design and consistent execution. • Partner cross-functionally with Quality, Regulatory Affairs, Manufacturing, Operations, R&D, Supply Chain, and other stakeholders to promote operational excellence, accountability, and a strong culture of quality.

🎯 Requirements

• Bachelor's degree in Quality, Engineering, Life Sciences, Biology, Regulatory Affairs, or a related field; advanced degree such as an MBA, MS, or equivalent is preferred. • 10+ years of experience in Quality Management Systems, quality assurance, regulatory compliance, or regulated manufacturing environments, including demonstrated experience leading global or enterprise-wide QMS harmonization. • 7+ years of leadership experience managing global or enterprise-level Quality or QMS teams in a complex, matrixed organization. • Expert-level knowledge of global QMS design, governance, deployment, lifecycle management, and regulatory frameworks such as FDA, ISO 9001, ISO 13485, ISO 17025, GMPs, HACCP, and comparable international standards. • Experience in regulated industries such as animal health, diagnostics, food safety, pharmaceutical, biotech, medical device, or regulated manufacturing environments. • Strong executive communication, stakeholder management, and influencing skills, with the ability to communicate risk, trade-offs, recommendations, and quality system priorities to senior leaders across regions and functions.

🏖️ Benefits

• A standard benefits package designed to support employee well-being. • An inclusive, professional work environment where quality, accountability, and continuous improvement are central to success.