Senior Site Quality Leader — Compliance, Audits & CI

Neogen Corporation; Lexington (KY); On-site; USD 120,000 - 180,000; Full time

Benefits offered by this job

Standard benefits package

Reasonable accommodations

Job summary

Neogen Corporation in Lexington, KY, is seeking a Senior Manager, Site Quality to lead quality assurance and quality control at our Lexington site. This role shapes site-level strategy, strengthens quality culture, and develops a high-performing team to support product quality and regulatory compliance.

The candidate will oversee the site Quality Management System, drive CAPA and continuous improvement, and partner across Manufacturing, Supply Chain, Regulatory Affairs, Engineering, and R&D to

Qualifications

• Proven leadership of large quality teams in manufacturing.
• Deep understanding of QA/QC, GMP, ISO, and regulatory audits.
• Experience implementing site-level quality systems and metrics.

Responsibilities

• Lead site quality operations and teams to align with policies and regulatory requirements.
• Maintain and improve site Quality Management System, procedures, and metrics.
• Serve as primary quality representative for audits (internal, customer, regulatory, certifications).
• Lead root cause investigations and CAPA initiatives for continuous improvement.
• Collaborate with Manufacturing, Supply Chain, Regulatory Affairs, Engineering, R&D, and Operations on changes and launches.
• Recruit, coach, and develop quality staff and manage performance.

Skills

Leadership

Quality management

Quality assurance

Quality control

Manufacturing

Regulatory compliance

Education

Bachelor’s degree in Quality/Engineering/Life Sciences

ASQ certification

Lean Six Sigma certification

Job description

Neogen Corporation in Lexington, KY, is seeking a Senior Manager, Site Quality to lead quality assurance and quality control at our Lexington site. This role shapes site-level strategy, strengthens quality culture, and develops a high-performing team to support product quality and regulatory compliance.

The candidate will oversee the site Quality Management System, drive CAPA and continuous improvement, and partner across Manufacturing, Supply Chain, Regulatory Affairs, Engineering, and R&D to