Analytical Data Reviewer – LNP and Lipids

## Company Description The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we focus on your professional growth by providing opportunities to build a rewarding career within the biopharmaceutical industry. Our supportive teams, comprehensive training, and commitment to work-life balance allow employees to develop their skills while contributing to meaningful scientific advancements. Eurofins Scientific is an international life sciences company providing a unique range of analytical testing services to clients across multiple industries, helping make life and our environment safer, healthier, and more sustainable. From the food you eat to the medicines you rely on, Eurofins works with some of the world's largest companies to ensure product safety, authenticity, and quality. Join us in shaping a safer, healthier, and more sustainable world. Explore opportunities with Eurofins and become part of a global team driving scientific excellence. ## Job Description Eurofins PSS is seeking an **Analytical Data Reviewer – LNP and Lipids** to support analytical quality and compliance activities for lipid nanoparticle (LNP) formulations and lipid-based materials in a GMP-regulated environment. This non-laboratory position is responsible for the detailed review and evaluation of analytical data generated from stability studies, method development activities, and laboratory investigations. The ideal candidate will possess strong analytical chemistry knowledge, experience reviewing chromatographic data, and a commitment to data integrity and regulatory compliance. Responsibilities - Review analytical data packages related to LNP formulations, lipid raw materials, stability studies, method development, and investigations. - Evaluate chromatographic and analytical data generated from techniques such as HPLC, UPLC, and LC-MS for accuracy, completeness, and compliance. - Verify calculations, data transcriptions, instrument outputs, and supporting documentation. - Review OOS (Out-of-Specification) and OOT (Out-of-Trend) investigations for scientific soundness, completeness, and appropriate corrective actions. - Ensure all records comply with GMP requirements, Good Documentation Practices, and applicable regulatory guidelines. - Maintain review timelines and tracking systems to support sample release and regulatory submission milestones. - Collaborate with Analytical Development, Quality Control, and Quality Assurance teams to address data discrepancies and resolve review findings. - Support continuous improvement initiatives related to data review processes and compliance practices. ## Qualifications **Minimum Qualifications** - Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline. - 3-4 years of analytical laboratory experience within a GMP-regulated pharmaceutical, biotechnology, or biopharmaceutical environment. - Experience generating and interpreting chromatographic data, including HPLC, UPLC, and/or LC-MS. - Working knowledge of GMP regulations, data integrity principles, and Good Documentation Practices. - Strong attention to detail and ability to identify inconsistencies within analytical datasets and documentation. - Excellent organizational, time management, and multitasking skills. - Ability to work both independently and collaboratively within cross-functional teams. - Strong written and verbal communication skills. **Preferred Qualifications** - Experience reviewing analytical data within a QC, QA, or analytical development environment. - Familiarity with lipid nanoparticle (LNP) technologies, lipid characterization, and related investigations. - Experience supporting analytical method development or method lifecycle activities. - Experience with electronic systems such as Veeva, SLIMS, JMP, LIMS, or similar laboratory software platforms. - Authorization to work in the United States indefinitely without restriction or sponso…