Analytical Characterization Development Scientist - LNPs
Listed on 2026-07-15
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Research/Development
Pharmaceutical Science/ Research, Research Scientist, Biotech Research
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 and provide opportunities to break into the biopharmaceutical industry. We offer supportive teams, tools for your development, work‑life balance, and a competitive benefits package.
Eurofins Scientific is an international life sciences company providing analytical testing services across multiple industries to enhance safety, health, and sustainability. We partner with major global firms to ensure product safety, authenticity, and accurate labeling. Eurofins is a global leader in food, environmental, pharmaceutical, and cosmetic testing, as well as independent market leader in genomics, discovery pharmacology, forensics, CDMO, advanced materials, and clinical study support.
Job DescriptionEurofins is seeking a highly skilled, passionate, and motivated scientist to join our client Analytical Development team. The role involves supporting testing of non‑GMP samples for development studies, including comparability assessments, process development, stability, product, and process characterization. The analytical team develops and implements new analytical methods and optimizes existing methods for raw materials, RNA drug substances, and LNP products at various development stages.
Responsibilities- Provide testing support for release, stability, product characterization, high‑throughput analysis, and 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.
- Collaborate actively with internal and external process development and quality teams.
- Train and mentor junior team members as needed.
Minimum Qualifications
- 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 LCs.
- Proficiency with software systems such as Open Lab, Empower, and ELN (Benchling is a plus).
- Previous experience developing methods for mRNA, gRNA, LNP, or lipids.
- 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 in analytical methodologies such as IP‑RP, IEX, and AEX.
- Experience with 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.
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.
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