QA Data Review Associate

Eurofins; Columbia Township (MO); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Medical, dental, and vision coverage

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA BioPharma Services in Columbia, MO is hiring a QA Data Review Associate to verify laboratory data, review reports, and ensure regulatory compliance. You will work with laboratory and quality teams to maintain accuracy, traceability, and quality documentation.

This is a full-time role with a Monday–Friday schedule, offering comprehensive benefits and opportunities to grow in quality assurance and data review within the pharmaceutical and life sciences field.

Qualifications

• Bachelor's degree in Chemistry, Biology, Biochemistry, Pharmaceutical Science, Chemical Engineering, or a related scientific discipline.
• Ability to work in the United States without current or future sponsorship requirements.
• Strong attention to detail and organizational skills.
• Excellent written and verbal communication abilities.
• Ability to learn new processes quickly and manage multiple priorities in a fast-paced environment.

Responsibilities

• Review laboratory reports, data packages, and supporting documentation for accuracy, completeness, and compliance.
• Partner with scientific teams to identify, communicate, and resolve data discrepancies or quality concerns.
• Support quality system activities including CAPA investigations, change controls, training records, and procedural updates.
• Review protocols, methods, reports, and SOPs to ensure alignment with regulatory and client requirements.
• Evaluate corrective actions and assess potential compliance impacts.
• Communicate findings effectively with laboratory personnel and clients when needed.
• Monitor quality metrics and contribute to continuous improvement efforts.
• Maintain a strong commitment to safety, accuracy, and regulatory compliance.

Skills

Attention to detail

Organizational skills

Strong written and verbal comms

Fast learner

Education

Bachelor's degree in Chemistry/Biology/Pharmaceutical Science

Job description

At Eurofins, your work helps make the world safer and healthier. From ensuring the safety of medicines and medical devices to verifying the quality of food, water, and consumer products, our scientists and laboratory professionals support industries that impact millions of lives every day.

As a global leader in laboratory testing and scientific services, Eurofins operates more than 900 laboratories across 54 countries and employs over 58,000 professionals dedicated to advancing science, quality, and innovation. Our teams work with many of the world's leading pharmaceutical, biotechnology, environmental, and consumer product companies to deliver trusted results that make a real difference.

Whether you're launching your career or building on existing experience, Eurofins offers the opportunity to grow, learn, and contribute to meaningful work in a collaborative and science-driven environment.

Job Description

Are you a detail-oriented science graduate who enjoys reviewing data, ensuring accuracy, and maintaining quality standards? Join Eurofins as a QA Data Review Associate, where you'll play a critical role in verifying laboratory data and documentation that supports the safety and quality of products used around the world.

In this position, you'll review laboratory reports, scientific data, protocols, and quality records to ensure accuracy, completeness, traceability, and compliance with established procedures and regulatory requirements. You'll work closely with laboratory and quality teams to identify and resolve discrepancies, support quality systems such as CAPAs and change controls, and help maintain the high standards our clients expect.

This is an excellent opportunity for recent graduates and early-career professionals seeking to build a career in quality assurance, compliance, data review, or laboratory operations within the pharmaceutical and life sciences industry.

What You'll Do

• Review laboratory reports, data packages, and supporting documentation for accuracy, completeness, and compliance.
• Partner with scientific teams to identify, communicate, and resolve data discrepancies or quality concerns.
• Support quality system activities including CAPA investigations, change controls, training records, and procedural updates.
• Review protocols, methods, reports, and SOPs to ensure alignment with regulatory and client requirements.
• Evaluate corrective actions and assess potential compliance impacts.
• Communicate findings effectively with laboratory personnel and clients when needed.
• Monitor quality metrics and contribute to continuous improvement efforts.
• Maintain a strong commitment to safety, accuracy, and regulatory compliance.
• Perform additional quality-related responsibilities as assigned.

Qualifications

Required Qualifications

• Bachelor's degree in Chemistry, Biology, Biochemistry, Pharmaceutical Science, Chemical Engineering, or a related scientific discipline.
• Ability to work in the United States without current or future sponsorship requirements.
• Strong attention to detail and organizational skills.
• Excellent written and verbal communication abilities.
• Ability to learn new processes quickly and manage multiple priorities in a fast-paced environment.

Ideal Candidates Will Have

• An interest in quality systems, compliance, and regulated laboratory environments.
• Strong critical thinking and problem-solving skills.
• A collaborative mindset and a passion for producing high-quality work.

Additional Information

Position is full-time position, Monday - Friday 8:00am - 4:30pm. Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply.

Excellent full time benefits including

• Comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays

Build a career where quality matters.

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.