Stability Scientist

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  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.

Job Description Eurofins BPT-Columbia is seeking a Stability Scientist to join our Stability and Batch Release team in Columbia, Missouri. This position is ideal for an early-career scientist interested in pharmaceutical quality testing, stability programs, and GMP laboratory operations.

The Stability Scientist is responsible for performing routine and non-routine analytical testing to support product stability studies and batch release activities. Working within a GMP-regulated laboratory environment, this individual will execute testing according to established methods, protocols, and standard operating procedures while ensuring accurate documentation and data integrity. The successful candidate will gain experience with analytical instrumentation, laboratory investigations, and regulatory-compliant testing while working both independently and collaboratively within a team environment.

Key Responsibilities:

Perform analytical testing in support of product stability studies and batch release programs.

Operate and maintain laboratory instrumentation such as HPLC, GC, and other analytical systems.

Prepare samples, reagents, standards, and documentation in accordance with established procedures.

Accurately collect, review, and document data following GMP and/or GLP requirements.

Support study execution, data review, troubleshooting activities, and report generation.

Maintain laboratory organization and compliance with safety and quality standards.

Collaborate with team members to meet project timelines and client expectations.

Work with increasing independence on assignments while seeking guidance as needed.

Qualifications Experience working in a GMP and/or GLP laboratory environment.

Hands-on analytical chemistry experience with HPLC and/or GC instrumentation.

Familiarity with laboratory information management systems (LIMS).Strong attention to detail and documentation practices.

Excellent organizational, communication, and time-management skills.

A desire to grow within pharmaceutical analytical testing and quality operations.

Authorization to work in the United States indefinitely without restriction or sponsorship.

Additional Information Position is full-time, working Monday-Friday, 8:00 a.m.

-4:30 p.m., some weekend required overtime as needed. Candidates currently living within commutable distance to Columbia, MOare encouraged to apply.

What we Offer:

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 Bio Pharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Summary Type:
Full-time Function:
Science Experience level:
Associate Industry: Biotechnology