Neogen

Senior Quality Manager

Neogen$90K — $120K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Quality, Engineering, Biology, Microbiology, Food Science, Animal Science, Life Sciences, or a related field.
  • 10+ years of experience in quality assurance, quality control, manufacturing, or regulatory environments.
  • 5+ years of people management experience, demonstrating leadership in team development.
  • Industry experience in animal health, diagnostics, food safety, pharmaceutical, biotech, or manufacturing sectors.
  • Knowledge of ISO, GMP, HACCP, FDA, USDA, or similar regulatory standards.
  • ASQ or Lean Six Sigma certification preferred.

Responsibilities

  • Lead site quality operations and align initiatives with company policies and regulatory standards.
  • Maintain and enhance the site's quality management system and related documentation.
  • Act as the main quality contact for audits and compliance checks at the Lexington site.
  • Conduct root cause analyses, corrective actions, and drive improvements for compliance and efficiency.
  • Collaborate with various departments to support process validations and product launches.
  • Develop and engage a high-performing quality team through coaching and performance management.

Benefits

  • Senior leadership role with significant site quality and operational impact.
  • Opportunity to work with cross-functional teams in a manufacturing setting.
  • Focus on continuous improvement and strengthening quality systems.
  • Standard benefits package provided.
  • Accommodations available for qualified individuals with disabilities.
Full Job Description
We are seeking a Senior Manager, Site Quality to lead quality assurance and quality control operations at our Lexington site. In this highly visible leadership role, you will oversee site quality systems, ensure compliance with applicable regulatory and industry standards, and partner across Operations, Manufacturing, Supply Chain, Regulatory Affairs, Engineering, and R&D to support product quality, operational excellence, and continuous improvement. This is an opportunity for an experienced quality leader to shape site-level strategy, strengthen quality culture, and develop a high-performing team.

Key Responsibilities
  • Lead all site quality operations, initiatives, and team activities to ensure alignment with company policies, customer expectations, and applicable regulatory requirements.
  • Maintain and improve the site quality management system, including quality procedures, documentation practices, metrics, and performance indicators.
  • Serve as the primary quality representative for the Lexington site, including preparation and support for internal, customer, certification, and regulatory audits.
  • Lead root cause investigations, corrective and preventive action initiatives, and continuous improvement efforts to enhance quality, efficiency, and compliance.
  • Partner cross-functionally with Manufacturing, Supply Chain, Regulatory Affairs, Engineering, R&D, and Operations to support process changes, validations, product launches, supplier quality activities, and issue resolution.
  • Recruit, coach, develop, and engage quality team members while supporting performance management, accountability, and succession planning.
Job Requirements
  • Bachelor's degree in Quality, Engineering, Biology, Microbiology, Food Science, Animal Science, Life Sciences, or a related field.
  • 10+ years of experience in quality assurance, quality control, manufacturing, or regulatory environments, including experience in a manufacturing or production setting.
  • 5+ years of people management experience, with a demonstrated ability to lead, coach, and develop teams.
  • Experience in animal health, diagnostics, food safety, pharmaceutical, biotech, or manufacturing industries.
  • Working knowledge of ISO, GMP, HACCP, FDA, USDA, or related regulatory standards.
  • ASQ certification and/or Lean Six Sigma certification preferred.
What We Offer
  • A senior leadership opportunity with meaningful impact on site quality, compliance, and operational performance.
  • Collaboration with cross-functional teams in a manufacturing-focused environment.
  • Opportunities to drive continuous improvement, strengthen quality systems, and develop team capability.
  • A standard benefits package.
  • Reasonable accommodations may be provided to enable qualified individuals with disabilities to perform the essential functions of the role.

If you are a quality leader who is committed to compliance, continuous improvement, and building strong teams, we'd love to hear from you. Join our team and help advance a culture of quality and operational excellence at the Lexington site.

About Neogen

Neogen Corporation is a publicly traded company that develops and markets products for food and animal safety. The company was founded in 1982 and is headquartered in Lansing, Michigan. Neogen's products include diagnostic test kits for foodborne pathogens, allergens, and drugs, as well as veterinary instruments and pharmaceuticals. The company's customers include food and beverage producers, animal producers, and veterinary clinics. Neogen has operations in the United States, Canada, Mexico, Europe, and Asia. The company has been recognized for its innovation and has received numerous awards for its products and services.
Learn more about Neogen
Size
1,841 employees
Market Cap
$3.2 billion
Industry
Net Income
$60.2 million
Founded
1982
5 Year Trend
+8%
Revenue
$433.2 million
NASDAQ

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