QA Associate I: Drive Accurate, Compliant Lab Reports

Eurofins; Columbia Township (MO); On-site; USD 55,000 - 90,000; Full time

Benefits offered by this job

Comprehensive medical coverage

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA BioPharma Services in Columbia, MO is seeking a Quality Assurance professional to review client laboratory reports, ensure accuracy and traceability, and support quality systems. The role emphasizes collaboration with scientific staff to resolve comments and maintain compliance with regulatory standards.

You will participate in CAPA activities, change controls, and trainings while ensuring adherence to SOPs and project plans, contributing to safe and compliant laboratory operations.

Qualifications

• Bachelor's degree in a relevant field or coursework is required.
• Authorization to work in the United States indefinitely without sponsorship.

Responsibilities

• Meets quality and productivity metrics and collaborates with staff to ensure accuracy and completeness of reports.
• Reviews client laboratory reports and related records for accuracy and traceability; addresses deficiencies for clarification and compliance.
• Assists with implementation and monitoring of quality systems and procedures (e.g., CAPA, change controls, trainings).
• Reviews protocols, procedures, data, reports to ensure compliance with regulatory requirements and SOPs.
• Keeps supervisor informed of significant issues identified during QA activities.
• Communicates with scientific staff to resolve comments and complete tasks within production quotas.

Skills

Teamwork

Communication

Attention to detail

Education

Bachelor's degree in chemistry/biochemistry/biology/chemical engineering/pharmaceutical science

Job description

Eurofins USA BioPharma Services in Columbia, MO is seeking a Quality Assurance professional to review client laboratory reports, ensure accuracy and traceability, and support quality systems. The role emphasizes collaboration with scientific staff to resolve comments and maintain compliance with regulatory standards.

You will participate in CAPA activities, change controls, and trainings while ensuring adherence to SOPs and project plans, contributing to safe and compliant laboratory operations.