Associate Scientist - Data Review

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 DoReview scientific reports and supporting documentation to ensure compliance with cGMP requirementsVerify that data is complete, accurate, and scientifically soundServe as a quality-focused partner to laboratory operations teamsParticipate in and support internal quality auditsContribute to maintaining high standards of data integrity and regulatory complianceProvide final quality review and report approval before client releaseAssist with additional Quality Assurance activities as neededQualificationsPreferred QualificationsExperience working in a laboratory or GMP-regulated environmentStrong organizational and time management skillsExcellent written and verbal communication abilitiesHigh attention to detail and commitment to qualityAbility to work independently while collaborating effectively with cross-functional teamsStrong computer skills and comfort reviewing technical documentationPositive attitude, adaptability, and willingness to learnAbility to manage multiple priorities while maintaining accuracyMinimum QualificationsBachelor's degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, Chemical Engineering, or a closely related scientific disciplineAuthorization to work in the United States indefinitely without sponsorshipAdditional 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 optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysEurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.SummaryType: Full-timeFunction: ScienceExperience level: AssociateIndustry: Biotechnology