Associate Scientist - Data Review
Eurofins BioPharma Product Testing North America
Summary
Eurofins BioPharma Product Testing Columbia is seeking an Associate Scientist, Data Review to join our Quality Assurance team. 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.
Job description
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
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
Requirements
- 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
- Experience working in a laboratory or GMP-regulated environment (preferred)
- 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
- Ability to manage multiple priorities while maintaining accuracy
Benefits
- Medical, Dental & Vision
- Life Insurance
- Disability Insurance
- 401(k) Matching
- Paid Vacation
- Paid Holidays
Company overview
Eurofins BioPharma Product Testing North America is the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide, providing comprehensive laboratory services for pharmaceutical, biopharmaceutical, and medical device companies. As a leading Contract Research Organization (CRO), the company offers extensive testing capabilities for drug substances, final products, intermediates, and starting materials for both small and large molecule drug products. Operating under GMP authorization, ISO 17025 accreditation, and ISO 9000 certification, Eurofins performs analyses according to international pharmacopeial standards including Ph. Eur., BP, USP, and JP. With over 2 million square feet of global laboratory capacity spanning 20 countries and more than 45 locations worldwide, the company maintains seven key US sites in Lancaster, PA; Portage, MI; Columbia, MO; Cary, NC; Charlotte, NC; Jacksonville, FL; and San Diego, CA. Their comprehensive service portfolio includes method development and validation, release testing, stability testing, characterization testing, residuals and impurities testing, extractables and leachables testing, viral clearance studies, and cell and gene therapy testing. The company's harmonized quality procedures, centralized LIMS, and secure 24-hour data access via LabAccess.com provide clients with consistent, reliable testing services that support drug development from early stages through commercialization.