Laboratory Data Review Associate

Eurofins USA BioPharma Services • Columbia, MO

7d • Onsite

About The Position

Eurofins BPT-Columbia is seeking an entry-level Laboratory Data Review Associate to join its Quality Assurance team in Columbia, Missouri. This is an onsite role in a regulated laboratory environment and is not a data science, data analytics, or programming position. The associate works with laboratory and quality teams to review scientific reports, data, and documentation for accuracy, completeness, and compliance with company, client, and regulatory requirements.

The role offers an opportunity to gain experience in a regulated laboratory environment and develop expertise in scientific data review, compliance, and quality systems while working alongside scientists and quality professionals. Relocation assistance is not available, and candidates within commuting distance of Columbia are encouraged to apply.

Requirements

• 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.

Nice To Haves

• 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.

Responsibilities

• Review laboratory reports and supporting documentation for accuracy, completeness, and compliance with GMP and quality requirements.
• Verify 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.

Benefits

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level