Company DescriptionEurofins 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 DescriptionAre 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
QualificationsPreferred 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 InformationWorking 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. 
