QA Data Review Associate
Eurofins BioPharma Product Testing North America
Summary
Are you a detail-oriented science graduate who enjoys reviewing data, ensuring accuracy, and maintaining quality standards? Join Eurofins as a QA Data Review Associate, where you'll play a critical role in verifying laboratory data and documentation that supports the safety and quality of products used around the world.
Job description
In this position, you'll review laboratory reports, scientific data, protocols, and quality records to ensure accuracy, completeness, traceability, and compliance with established procedures and regulatory requirements. You'll work closely with laboratory and quality teams to identify and resolve discrepancies, support quality systems such as CAPAs and change controls, and help maintain the high standards our clients expect.
This is an excellent opportunity for recent graduates and early-career professionals seeking to build a career in quality assurance, compliance, data review, or laboratory operations within the pharmaceutical and life sciences industry.
What You'll Do
- Review laboratory reports, data packages, and supporting documentation for accuracy, completeness, and compliance.
- Partner with scientific teams to identify, communicate, and resolve data discrepancies or quality concerns.
- Support quality system activities including CAPA investigations, change controls, training records, and procedural updates.
- Review protocols, methods, reports, and SOPs to ensure alignment with regulatory and client requirements.
- Evaluate corrective actions and assess potential compliance impacts.
- Communicate findings effectively with laboratory personnel and clients when needed.
- Monitor quality metrics and contribute to continuous improvement efforts.
- Maintain a strong commitment to safety, accuracy, and regulatory compliance.
- Perform additional quality-related responsibilities as assigned.
Qualifications
Required Qualifications
- Bachelor's degree in Chemistry, Biology, Biochemistry, Pharmaceutical Science, Chemical Engineering, or a related scientific discipline.
- Ability to work in the United States without current or future sponsorship requirements.
- Strong attention to detail and organizational skills.
- Excellent written and verbal communication abilities.
- Ability to learn new processes quickly and manage multiple priorities in a fast-paced environment.
Ideal Candidates Will Have
- An interest in quality systems, compliance, and regulated laboratory environments.
- Strong critical thinking and problem-solving skills.
- A collaborative mindset and a passion for producing high-quality work.
Requirements
- Bachelor's degree in Chemistry, Biology, Biochemistry, Pharmaceutical Science, Chemical Engineering, or a related scientific discipline.
- Ability to work in the United States without current or future sponsorship requirements.
- Strong attention to detail and organizational skills.
- Excellent written and verbal communication abilities.
- Ability to learn new processes quickly and manage multiple priorities in a fast-paced environment.
- Interest in quality systems, compliance, and regulated laboratory environments.
- Strong critical thinking and problem-solving skills.
- Collaborative mindset and a passion for producing high-quality work.
Benefits
- Medical Coverage
- Dental Coverage
- Vision Coverage
- Life Insurance
- Disability Insurance
- 401(k) With Company Match
- 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.