Associate Director, Quality Assurance - ISO 17025 Leader

Eurofins; Madison (WI); On-site; USD 130,000 - 170,000; Full time

Benefits offered by this job

Excellent benefits package

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA Food Testing in Madison, WI is seeking an Associate Director of Quality Assurance on site to lead quality programs across laboratories. You will support Quality team members, supervise staff, ensure SOP adherence, and drive timely, compliant results under ISO 17025 and FDA guidelines.

The role requires at least 7 years in QA, experience with GMP/GLP, audits, CAPA, and strong communication. Travel up to 30% and residence within commutable distance to Madison is expected.

Qualifications

• Experience implementing and maintaining QMS in ISO 17025 environments.
• Strong documentation and SOP writing abilities with attention to detail.
• Familiarity with regulatory requirements (FDA) and GMP/GLP principles.

Responsibilities

• Demonstrates and promotes the company vision, mission, and quality objectives.
• Applies GMP/GLP in all areas of responsibility and ensures SOP adherence.
• Maintains ISO certification activities and coordinates audit scheduling and scope changes.
• Reviews and ensures implementation of new/revised controlled documents.
• Leads quality improvement projects with broad Eurofins benefits.
• Monitors metrics (non-conformances, deviations, CAPA) and conducts root-cause analysis.
• Oversees PT program and monthly metric reporting; answers client inquiries on quality matters.

Skills

Quality management

GMP/GLP

Audits

CAPA

Documentation & SOP writing

Data analysis

Communication

Travel readiness

Education

Bachelor's degree in science

Tools

LIMS

QA software

Job description

Eurofins USA Food Testing in Madison, WI is seeking an Associate Director of Quality Assurance on site to lead quality programs across laboratories. You will support Quality team members, supervise staff, ensure SOP adherence, and drive timely, compliant results under ISO 17025 and FDA guidelines.

The role requires at least 7 years in QA, experience with GMP/GLP, audits, CAPA, and strong communication. Travel up to 30% and residence within commutable distance to Madison is expected.