Quality Assurance Supervisor

Neogen Corporation • Lexington, KY

62d • Onsite

About The Position

We are seeking a Quality Assurance Supervisor based in Lexington, Kentucky to oversee quality validation processes for equipment and systems, support regulatory compliance, and drive continuous improvement across established quality programs. This role is ideal for a detail-oriented leader who can guide teams, review procedures, and ensure quality practices align with internal standards and current industry expectations.

Requirements

• Bachelor's degree in a relevant field such as Quality Assurance, Engineering, Life Sciences, or a related discipline, or equivalent professional experience.
• Experience in quality assurance, validation, compliance, or a related function within a regulated industry.
• Working knowledge of applicable regulatory requirements, quality systems, validation principles, and industry current practices.
• Ability to review technical documentation, identify compliance risks, and recommend practical process improvements.
• Strong organizational, communication, and problem-solving skills, with attention to detail.
• Demonstrated ability to lead, coach, or supervise team members in a professional environment.

Responsibilities

• Direct and support the development, execution, and documentation of validation activities for equipment, systems, and related processes.
• Oversee quality assurance procedures to help ensure compliance with applicable regulatory requirements, internal standards, and industry best practices.
• Review validation protocols, reports, deviations, and related documentation for accuracy, completeness, and compliance.
• Evaluate existing quality and validation processes, recommending improvements to enhance efficiency, consistency, and compliance readiness.
• Collaborate with cross-functional teams, including operations, engineering, and regulatory stakeholders, to support quality objectives.
• Provide day-to-day supervision, guidance, and technical support to team members involved in quality validation activities.

Benefits

• Standard benefits package.
• The opportunity to contribute to quality systems and validation practices in a regulated professional setting.
• A collaborative work environment where process improvement, compliance, and operational excellence are valued.
• A mid-level supervisory role with meaningful responsibility and cross-functional visibility.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level