Additionalinformation

Additional Information

Candidates currently living within commuting distance of Columbia, Missouri are encouraged to apply. Relocation assistance is not available.

This is an on-site position and is not eligible for remote work.

What We Offer

• Comprehensive medical, dental, and vision insurance
• Life and disability insurance
• 401(k) with company match
• Paid holidays and vacation time
• Opportunities for professional growth and development within a global scientific organization

Why Join Eurofins?

Whether you're a recent science graduate or looking to begin a career in quality assurance, this role provides an excellent opportunity to gain experience in a regulated laboratory environment while developing expertise in scientific data review, compliance, and quality systems. You'll work alongside experienced scientists and quality professionals who help ensure the integrity and reliability of laboratory testing that impacts patients, consumers, and communities worldwide.

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

Companydescription

Company Description

Eurofins Scientific is an international life sciences company providing a unique range of analytical testing services to clients across multiple industries to make life and our environment safer, healthier, and more sustainable. From the food you eat to the medicines you rely on, Eurofins laboratories help ensure products are safe, authentic, and accurately labeled.

With over 58,000 employees across more than 900 laboratories in over 50 countries, Eurofins is a global leader in laboratory testing, pharmaceutical services, and scientific innovation.

Jobdescription

Job Description

This is NOT a Data Science, Data Analytics, or Programming Position.

Eurofins BPT-Columbia is seeking a Laboratory Data Review Associate to join our Quality Assurance team in Columbia, Missouri.

This entry-level role is ideal for those who enjoy reviewing scientific information, ensuring accuracy, and supporting quality processes in a regulated laboratory environment. The Laboratory Data Review Associate works closely with laboratory and quality teams to verify that scientific reports, data, and documentation meet company, client, and regulatory requirements.

Responsibilities

• Review laboratory reports and supporting documentation to verify accuracy, completeness, and compliance with GMP and quality requirements.
• Ensure scientific data is properly documented and meets established standards before final approval and release.
• Collaborate with laboratory operations and quality personnel to resolve discrepancies and clarify documentation.
• Assist with internal quality audits and quality system activities.
• Maintain accurate records and documentation in accordance with standard operating procedures.
• Support continuous improvement initiatives within the Quality Assurance department.
• Perform other related duties as assigned.

Qualifications

Preferred Qualifications

• Previous experience in a laboratory, quality assurance, quality control, or GMP-regulated environment.
• Strong attention to detail and organizational skills.
• Effective written and verbal communication abilities.
• Proficiency with computers and common business software applications.
• Ability to manage multiple priorities while maintaining accuracy.
• Self-motivated with the ability to work independently and as part of a team.
• Willingness to learn scientific processes, regulatory requirements, and quality systems.

Minimum Qualifications

• Bachelor's degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, Chemical Engineering, or another related scientific discipline.
• Ability to work in the United States indefinitely without current or future sponsorship.