Principal Scientist II, Investigations

Eurofins

Columbia, MO, United StatesFull-timePosted 4h ago

Get more Software Engineering openings

A short daily email when similar roles appear in Columbia. No account needed.

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 water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

2025, Eurofins generated total revenues of EUR € 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.

 

Job Description

Eurofins BPT-Columbia is seeking a Principal Scientist II to join the Investigations team within our Biochemistry department. This role focuses on leading and supporting laboratory investigations in a regulated cGMP environment.

The successful candidate will partner cross-functionally to identify root causes, drive corrective and preventive actions (CAPAs), and ensure timely resolution of quality and laboratory investigations. This position requires a strong technical understanding of analytical testing, excellent problem-solving skills, and the ability to manage multiple priorities in a fast-paced environment.

Key Responsibilities

  • Conduct and support laboratory investigations in compliance with cGMP and GLP requirements.
  • Perform root cause analyses using tools such as Fishbone Diagrams and 5 Whys.
  • Lead and document deviations, investigations, and CAPAs through completion.
  • Collaborate with Quality, Operations, Analytical Development, and other departments to resolve issues within established timelines.
  • Review data and documentation to ensure accuracy, quality, and regulatory compliance.
  • Assess analytical results generated using techniques such as HPLC, CE-SDS, icIEF, ELISA, and cell-based assays.
  • Maintain clear, thorough, and compliant documentation.
  • Manage multiple investigations and projects simultaneously while meeting deadlines.

Qualifications

The ideal candidate would possess:

  • Have practical knowledge of laboratory instrumentation (HPLC, CE-SDS, icIEF, ELISA, cell-based assays, etc.)
  • Experience with a LIMS system desirable.
  • Understanding of internal processes for investigational work.
  • Ability to assess root cause using fishbone or 5 why’s.
  •  Ability to drive CAPAs and Investigations to completion on tight timelines by working across multiple departments.
  • Attention to detail.
  • Ability to work on multiple on-going projects.

Minimum Qualifications:

  • Bachelor’s degree in relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field or degree with comparable coursework in the above areas.
  • 1-3 years of experience working in a cGMP compliant lab

Additional Information

The position is full-time, Monday-Friday, 8am-4:30pm, with overtime as needed. Candidates who live within a commutable distance from 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

 

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

The average job posting receives 250 applications.

Stand out by tailoring your resume to this specific role. Our AI resume builder highlights the skills and experience that matter most to this employer.

Frequently asked questions

Who is hiring for Principal Scientist II, Investigations at Eurofins?+
Eurofins is actively hiring for this Principal Scientist II, Investigations role. Click "Apply Now" to submit your application directly on Eurofins's careers page — Careeronaut doesn't charge employers or candidates for referrals.
When was this Principal Scientist II, Investigations role posted?+
This listing was first posted on 2026-11-04. We pull the latest copy from the source feed daily, and any role that's taken down gets removed from Careeronaut within seven days so you don't waste time on stale listings.
How should I apply to this Principal Scientist II, Investigations role?+
Start by tailoring your resume to the posting — most applicants send generic CVs and the first filter recruiters use is keyword relevance. Careeronaut's AI does this automatically: paste the job description, get a matched resume in under a minute, and download as PDF or DOCX.
Where can I find more Software Engineering jobs in Columbia?+
Browse all open software engineering roles in Columbia on the listing pages linked below. You can filter by salary, remote-friendly, and posting date.