QMS Global Director

Posted Yesterday
Be an Early Applicant
Hiring Remotely in USA
Remote
Expert/Leader
Biotech • Pharmaceutical
The Role
Lead enterprise-wide QMS strategy, governance, and continuous improvement. Drive harmonization, digital enablement, and regulatory compliance across global sites. Oversee CAPA, change control, document control, deviations, risk management, training, audit readiness, and regulatory inspections while partnering cross-functionally to advance quality system maturity and operational excellence.
Summary Generated by Built In

It's fun to work in a company where people truly believe in what they are doing!

As Global Director, Quality Management Systems (QMS), you will lead the enterprise-wide strategy, governance, and continuous improvement of global quality systems across regions and sites. Reporting to the VP of Global Quality, this Director-level role serves as the global QMS Center of Excellence leader and trusted advisor to senior leadership on quality system maturity, compliance, risk, and operational capability. This is an opportunity to shape a scalable, standardized, and future-ready QMS in a highly regulated global environment.

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!

From inside the farm gate to our dinner plates, Neogen protects the world’s food supply. Through a variety of animal healthcare products, to food safety solutions for dangerous bacteria, allergens, toxins, drug residues and much more, Neogen is there — and you can be too.

Skills Required

  • Bachelor's degree in Quality, Engineering, Life Sciences, Biology, Regulatory Affairs, or related field
  • Advanced degree (MBA, MS, or equivalent)
  • 10+ years experience in Quality Management Systems, quality assurance, regulatory compliance, or regulated manufacturing environments
  • Demonstrated experience leading global or enterprise-wide QMS harmonization
  • 7+ years leadership experience managing global or enterprise-level Quality or QMS teams
  • Expert-level knowledge of global QMS design, governance, lifecycle management, and regulatory frameworks (FDA, ISO 9001, ISO 13485, ISO 17025, GMPs, HACCP)
  • Experience in regulated industries such as animal health, diagnostics, food safety, pharmaceutical, biotech, medical device, or regulated manufacturing
  • Strong executive communication, stakeholder management, and influencing skills

Neogen Corporation Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Neogen Corporation and has not been reviewed or approved by Neogen Corporation.

  • Healthcare Strength The benefits suite includes comprehensive medical, dental and vision coverage, plus disability, life insurance, and an Employee Assistance Program. These core coverages are consistently described as a relative bright spot.
  • Retirement Support A defined-contribution 401(k) with company match and immediate vesting is highlighted, alongside standard retirement and savings programs. This structure provides clear baseline retirement support for eligible roles.
  • Equity Value & Accessibility An employee stock purchase plan offers discounted access to company shares. This adds an ownership pathway that complements cash compensation.

Neogen Corporation Insights

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The Company
HQ: Lansing, MI
1,160 Employees
Year Founded: 1982

What We Do

NEOGEN Corporation develops and markets products dedicated to food and animal safety. The company’s Food Safety Division markets dehydrated culture media and diagnostic test kits to detect foodborne bacteria, natural toxins, genetic modifications, food allergens, drug residues, plant diseases and sanitation concerns. NEOGEN’s Animal Safety Division markets a complete line of diagnostics, veterinary instruments, veterinary pharmaceuticals, nutritional supplements, disinfectants and rodenticides.

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