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Laboratory Operations Coordinator

Eurofins BioPharma Product Testing · Columbia, MO

Posted November 4, 2026

Mid levelGMPGLPOn site
Pay not postedApply

Quick facts

Experience
2+ years
Education
Bachelor's
Job type
Full-time
Schedule
Monday to Friday
Skills mentioned
GMP, GLP, Audits, LIMS, CRM (Salesforce/Veeva), Business development

Pulled from the ad below. The full ad has the details.

Job Description

Eurofins is seeking a highly organized and detail-oriented Laboratory Operations Coordinator to support scientific projects and laboratory operations within a fast-paced testing environment.

In this role, you will serve as a key link between clients and internal laboratory teams, coordinating project activities, managing timelines and documentation, facilitating communication, and ensuring testing programs progress efficiently from initiation through completion.

Responsibilities

  • Coordinate laboratory projects and studies to ensure timelines, deliverables, and client expectations are met.
  • Review project documentation including quotations, purchase orders, protocols, specifications, and client instructions to establish project requirements.
  • Create and maintain project records within Laboratory Information Management Systems (LIMS) and other internal systems.
  • Serve as the primary point of contact for assigned clients, providing project updates and facilitating routine status meetings.
  • Collaborate with laboratory operations, quality assurance, analytical testing groups, sample administration, finance, business development, and other internal stakeholders.
  • Monitor project timelines, milestones, deliverables, and open action items while proactively identifying potential risks.
  • Track project scope and coordinate change requests when additional services or requirements arise.
  • Support invoice review, billing milestones, and resolution of project-related discrepancies.
  • Resolve routine project issues and escalate complex challenges when necessary.
  • Maintain accurate, organized, and audit-ready project documentation.
  • Provide cross-functional support and backup coverage as assigned

Qualifications

Basic Minimum Qualifications

  • Bachelor's degree in Biology, Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, or a related scientific discipline.
  • Minimum of 2 years of professional experience in a laboratory, scientific, pharmaceutical, biotechnology, CRO, or project coordination environment.
  • Authorization to work in the United States indefinitely without restriction or sponsorship.

Preferred Qualifications

  • Experience coordinating laboratory projects, studies, or client deliverables.
  • Strong organizational and time-management skills with the ability to manage multiple priorities simultaneously.
  • Excellent communication and relationship-building skills.
  • Experience working with LIMS, eLIMS, eQMS, CRM systems, or similar platforms.
  • Proficiency with Microsoft Office applications.
  • Experience in pharmaceutical, biotechnology, analytical testing, or contract research environments.
  • Familiarity with GMP and/or GLP environments is preferred.

Additional Information

Position is Full-time, Monday-Friday, 8:00 a.m.-4:30 p.m. , with overtime as needed. 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

Join Eurofins and help support the scientific projects that contribute to safer products, healthier communities, and a more sustainable world.

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

Source: Eurofins BioPharma Product Testing's career site. PharmoniQ shows this job as posted and links to the original. Check the employer's page for the latest details.