Quality Assurance Validation Lead — Regulated Systems

Neogen; Lexington (KY); On-site; USD 80,000 - 110,000; Full time

Benefits offered by this job

Standard benefits package

Job summary

Neogen in Lexington, Kentucky is seeking a Quality Assurance Supervisor to oversee validation activities for equipment and systems, support regulatory compliance, and drive continuous improvement across quality programs.

You will lead teams, review validation protocols and reports, identify risks, and implement practical process improvements, collaborating with operations, engineering, and regulatory stakeholders to ensure quality objectives are met.

Qualifications

• Bachelor's degree or equivalent experience in Quality Assurance, Engineering, Life Sciences, or related field.
• Experience in quality assurance, validation, compliance, or related function within a regulated industry.
• Working knowledge of regulatory requirements, quality systems, validation principles, and industry practices.

Responsibilities

• Direct and support development, execution, and documentation of validation activities for equipment, systems, and related processes.
• Oversee quality assurance procedures to ensure compliance with regulatory requirements and internal standards.
• Review validation protocols, reports, deviations, and related documentation for accuracy and compliance.
• Evaluate existing quality and validation processes and recommend improvements for efficiency and consistency.
• Collaborate with cross-functional teams to support quality objectives.
• Provide day-to-day supervision and technical support to team members involved in quality validation activities.

Skills

Leadership

Team supervision

Quality assurance

Regulatory knowledge

Communication

Problem-solving

Education

Bachelor's degree or equivalent experience

Job description

Neogen in Lexington, Kentucky is seeking a Quality Assurance Supervisor to oversee validation activities for equipment and systems, support regulatory compliance, and drive continuous improvement across quality programs.

You will lead teams, review validation protocols and reports, identify risks, and implement practical process improvements, collaborating with operations, engineering, and regulatory stakeholders to ensure quality objectives are met.