QMS Global Director

Key Responsibilities 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.

Job 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.

What We Offer A Director-level global leadership opportunity with meaningful influence over enterprise quality strategy, governance, and operational excellence.

The opportunity to lead QMS transformation, modernization, and harmonization initiatives across a complex global organization. Collaboration with senior leaders and cross-functional teams across Quality, Regulatory Affairs, Manufacturing, Operations, R&D, Supply Chain, and other business areas.

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.

If you are an experienced quality systems leader with a strong background in global QMS governance, regulatory compliance, and enterprise transformation, we'd love to hear from you.

Join our team and help advance a global quality system that supports compliance, operational excellence, and long-term business growth. Come Be Part Of A Mission that Matters!

At Neogen, we are extremely proud of our record of sustained growth, as well as our development and acquisition of advanced technology since our founding in 1982.

Neogen has thrived - and will continue to thrive - because our employees thrive here.