Associate Scientist - Data Review

Eurofins US Network • Columbia, MO • 12h ago

Columbia, MO, USA

Full-time

Company Description

Eurofins Scientific is a global leader in analytical testing services, helping ensure the safety, authenticity, and quality of the food we eat, water we drink, medicines we rely on, and products we use every day.

With more than 58,000 employees across 900 laboratories in 54 countries , Eurofins provides over 200,000 analytical methods and supports some of the world's leading pharmaceutical, biotechnology, food, environmental, and consumer product companies.

Join a team where your scientific background, attention to detail, and commitment to quality can make a meaningful impact every day.

Ready to launch your quality assurance career in the pharmaceutical industry? Apply today and become part of a team dedicated to delivering science you can trust.

Job Description

Are you a detail-oriented science professional who enjoys ensuring quality, accuracy, and compliance? Do you like working closely with laboratory teams and being the final checkpoint before critical scientific data reaches clients? If so, Eurofins BioPharma Product Testing Columbia may be the perfect place to grow your career.

We are seeking an Associate Scientist, Data Review to join our Quality Assurance team in Columbia, Missouri. This entry-level opportunity is ideal for recent science graduates or laboratory professionals looking to transition into a quality-focused role within the pharmaceutical and biotechnology industry.

In this role, you'll play a critical part in maintaining the integrity of scientific data by reviewing laboratory reports, ensuring compliance with cGMP regulations, and collaborating with laboratory teams to support the delivery of high-quality results.

What You'll Do

Review scientific reports and supporting documentation to ensure compliance with cGMP requirements

Verify that data is complete, accurate, and scientifically sound

Serve as a quality-focused partner to laboratory operations teams

Participate in and support internal quality audits

Contribute to maintaining high standards of data integrity and regulatory compliance

Provide final quality review and report approval before client release

Assist with additional Quality Assurance activities as needed

Qualifications

Preferred Qualifications

Experience working in a laboratory or GMP-regulated environment

Strong organizational and time management skills

Excellent written and verbal communication abilities

High attention to detail and commitment to quality

Ability to work independently while collaborating effectively with cross-functional teams

Strong computer skills and comfort reviewing technical documentation

Positive attitude, adaptability, and willingness to learn

Ability to manage multiple priorities while maintaining accuracy

Minimum Qualifications

Bachelor's degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, Chemical Engineering, or a closely related scientific discipline

Authorization to work in the United States indefinitely without sponsorship

Additional Information

Working schedule will be Full-Time, First Shift, M-F 8am-4:30pm. Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply. No relocation assistance will be given. 25% travel may be required. This position is NOT remote.

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

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