Analytical Characterization Development Scientist - LNPs

Eurofins; Boston (MA); On-site; USD 50,971 - 56,481; Full time

Benefits offered by this job

Comprehensive medical coverage

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins is seeking a highly skilled scientist to join the Analytical Development team to support testing non-GMP samples for development studies such as comparability assessments, process development, stability, product, and process characterization. The team develops and implements new analytical methods for raw materials, RNA drug substances, and LNP products at various stages.

The role requires developing methods, interpreting data, and collaborating across teams, with opportunities to

Qualifications

• B.S. in Analytical Chemistry, Biochemistry, Biophysics, or related field with 3–4 years biotech experience using HPLC, LCMS or Capillary Electrophoresis.
• Proficiency with Waters and Agilent LCs.
• Proficiency with software systems such as OpenLab, Empower, and ELN.
• Experience developing methods for mRNA, gRNA, LNP, or lipids.
• Familiarity with ICH regulations and multi-compendial guidelines related to method validation.
• Experience in assay development, qualification, validation, and GMP transfer.
• Ability to balance multiple responsibilities, prioritize, and navigate ambiguity.
• Demonstrated learning agility, problem solving, and strong written/verbal communication.
• Proactive, creative, and positive attitude; commitment to safety.

Responsibilities

• Provide testing support for release, stability, product characterization, and high-throughput analysis.
• Collect, process, and analyze data with accurate documentation in ELN.
• Review, interpret, and present data within analytical and cross-functional teams.
• Author, review, and revise technical documents for comparability.
• Provide technical oversight to guide analytical/QC investigations.
• Collaborate with internal and external process development and quality teams.
• Train and mentor junior team members as needed.

Skills

Problem solving

Scientific communication

Prioritization

Team collaboration

Education

Bachelor's degree in Analytical Chemistry, Biochemistry, Biophysics, or related field

Tools

Waters LCs

Agilent LCs

OpenLab

Empower

ELN

Job description

Job Description

Eurofins is seeking a highly skilled, passionate, and motivated scientist to join our client Analytical Development team to support testing non‑GMP samples for development studies such as comparability assessments, process development, stability, product, and process characterization. The Analytical Development team is responsible for developing and implementing new analytical methods, as well as optimizing and improving current methods for the characterization of raw materials, RNA drug substances, and LNP products and programs at various development stages.

Responsibilities

• Provide testing support for a variety of purposes, including release and stability testing, product characterization, high-throughput analysis, and characterization of complex raw materials.
• Collect, process, and analyze experimental data, ensuring accurate and timely documentation in electronic laboratory notebook.
• Review, interpret, and present data within the analytical team and cross-functionally.
• Author, review, and revise technical source documents to support phase-appropriate comparability.
• Provide technical oversight to guide analytical/QC investigations, as needed.
• Actively collaborate with internal and external process development and quality teams.
• Train and mentor junior team members as needed.

Basic Minimum Qualifications

• B.S. in Analytical Chemistry, Biochemistry, Biophysics, or related field with 3‑4 years of biotech industry experience utilizing HPLC, LCMS, or Capillary Electrophoresis.
• Proficiency with instrumentation such as Waters and Agilent LCs.
• Proficiency with software systems such as OpenLab, Empower, and ELN (Benchling is a plus).
• Previous experience developing methods for mRNA, gRNA, LNP, or lipids in general.
• Familiarity with applicable ICH regulations and multi‑compendial guidelines related to method validation.
• Experience in assay development, qualification, validation, and transfer to GMP environments.
• Ability to balance multiple responsibilities, prioritize activities, and navigate ambiguity.
• Demonstrated learning agility, scientific problem solving, and strong written and verbal communication skills.
• Proactive, creative, and positive attitude.
• Unwavering commitment to safety protocols and procedures.

Preferred Qualifications

• Strong technical background on analytical methodologies using IP‑RP, IEX, and AEX.
• Experience working with various biophysical instrumentation such as GC, HIAC, and basic particle size characterization fluorescence-based assays.
• Strong understanding of SEC‑MALS analytical methodology.
• Authorization to work in the United States indefinitely without restriction or sponsorship.

Additional Information

The position is full‑time, first shift, Monday‑Friday with overtime as needed. Candidates living within a commutable distance of Boston, MA are encouraged to apply.

Benefits

• Comprehensive medical coverage, dental, and vision options.
• Life and disability insurance.
• 401(k) with company match.
• Paid vacation and holidays.
• Compensation: $37.00‑$41.00 per hour based on education and experience.

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