Analytical Data Reviewer – LNP and Lipids

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

• Bachelors 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 sponsorship.

Additional Information :

What to Expect in the Hiring Process: 

• 10-15 Minute Phone Interview with Region Recruiter
• 45-60 Minute Virtual Interview with Manager and/or Group Leader
• 30 Minute In-Person Onsite Meeting with the Team

Additional Details: 

The position is Full Time Monday-Friday 8am-5pm. Candidates currently living within a commutable distance of Boston MA are encouraged to apply.

Excellent full-time benefits include:

• Comprehensive medical coverage dental and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays
• Annual rate is between $36.00-$40.00 depending on education and experience 

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Remote Work :

No

Employment Type :

Full-time