Analytical Development Chemist

Company Overview

Eurofins Professional Scientific Services is an international life sciences company providing analytical testing services across multiple industries. We focus on employee professional growth and work‑life balance with a competitive benefits package.

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.

• 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 an 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.

• B.S. in Analytical Chemistry, Biochemistry, Biophysics, or a related field with 3-4 years of biotech industry experience utilizing HPLC, LCMS, or Capillary Electrophoresis.
• Proficiency with instrumentation such as Waters and Agilent liquid chromatographs.
• Proficiency with software systems such as Open Lab, Empower, and an electronic laboratory notebook (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.

• 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.

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.

• 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.