QA Data Review Associate
Columbia, MO, United States
- Pay
- Pay not listed
- Work setting
On-site — work setting source
Work setup in the employer’s listing: On-site
From the employer’s posting- Employment
Full-time — employment source
Employment type in the employer’s listing: Full-time
From the employer’s posting
Before you apply
- Sponsorship
Visa sponsorship not confirmed — sponsorship source
Ability to work in the United States without current or future sponsorship requirements.
Read the full posting
What you’ll work on
Full postingReview lab reports, data packages and supporting documents for accuracy and compliance
Identify and resolve data discrepancies or quality concerns with scientific teams
Support CAPA investigations, change controls, training records and procedure updates
Review protocols, methods, reports and SOPs against regulatory and client requirements
Evaluate corrective actions and assess potential compliance impacts
From the employer’s posting
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.
What you’ll bring
All qualificationsCore experience
- 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.
- Ability to learn new processes quickly and manage multiple priorities in a fast-paced environment.
Qualification wording
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.
Ability to learn new processes quickly and manage multiple priorities in a fast-paced environment.
Education & alternatives
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.
Posting record
Report an errorActively hiringFirst seen by us 5 days ago, still listed, and not a repost of an earlier listing.
- Status in our records
- Live
- First seen by us
- Oct 19, 2026 · 5 days ago
- Recorded sightings
- 31
- Last seen by us
- Oct 24, 2026
- Employer says posted
- Oct 13, 2026
These dates show when we found the listing. Check the employer’s website to confirm it is still accepting applications.
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- Have your resume and examples of relevant work ready.
- Check the listed location, eligibility and core experience before starting.
- Ask the employer about the pay range before committing time to the process.
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Job description
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.
If you're ready to apply your scientific background in a role that supports regulatory excellence and continuous improvement, we encourage you to apply today.
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
Company 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.
Source details
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- Pay
No pay amount identified in the saved description.
- Location & working pattern
Columbia, MO, United States
Working pattern and location restrictions need checking in the full posting.
- Work authorization
- 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.
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