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Open nowPosted 20 hours ago

Laboratory Operations Coordinator

Eurofins2,591 open roles

Where
Columbia, MO, United States
Work mode
On site
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Your applicationOpen nowLaboratory Operations CoordinatorEurofins · Columbia, MO, United States

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on Eurofins's own form.

The reply lands in your private mailbox

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The clock on this job

Early applications get read.

13.4% of postings close within 7 days. Measured by our own scanner across the market. Eurofins postings stay open a median of 19 days.

Share of postings closed within
  1. 2.2%1 day
  2. 4.6%3 days
  3. 13.4%7 days
  4. 21.6%14 days
  5. 36.2%30 days
  6. 59.0%60 days
This job: posted 20 hours ago

Eurofins median: 19 days open

The posting

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 product safety, quality, authenticity, and compliance.

With more than 58,000 employees across 900 laboratories in over 54 countries, Eurofins is a global leader in pharmaceutical, food, environmental, and consumer product testing.

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.

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