QA Data Review Associate

Eurofins USA BioPharma Services; Columbia Township (MO); In loco; USD 52.000 - 70.000; Tempo pieno

Vantaggi offerti da questo lavoro

Medical coverage

Dental coverage

Vision coverage

Life insurance

Disability insurance

401(k) with company match

Paid vacation and holidays

Descrizione del lavoro

Eurofins USA BioPharma Services in Columbia, MO is seeking a QA Data Review Associate to verify laboratory data and documentation ensuring safety and quality of products worldwide.

You will review reports, data packages, and quality records to ensure accuracy, traceability, and regulatory compliance. This role supports CAPAs, change controls, and continuous improvement with cross-functional teams.

Competenze

• Bachelor's degree in a scientific discipline as listed.
• Strong attention to detail and organizational skills.
• Excellent written and verbal communication abilities.
• Ability to learn new processes quickly and manage multiple priorities.

Mansioni

• Review laboratory reports, data packages, and supporting documentation for accuracy and compliance.
• Identify, communicate, and resolve data discrepancies or quality concerns with scientific teams.
• Support quality system activities including CAPA investigations and change controls.
• Review SOPs, methods, and reports to ensure alignment with regulatory and client requirements.
• Evaluate corrective actions and assess potential compliance impacts.
• Communicate findings with laboratory personnel and clients as needed.
• Contribute to continuous improvement by monitoring quality metrics.

Conoscenze

Attention to detail

Communication

Regulatory compliance

Data review

Team collaboration

Formazione

Bachelor's degree in Chemistry/Biology/Biochem/Pharmaceutical Science/related field

Descrizione del lavoro

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.