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.

• 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, ensure 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 .

Qualifications

_ Basic Minimum Qualifications:_

• B.S. in Analytical Chemistry, Biochemistry, Biophysics, or related field with at least 1 year of biotech industry experience or M.S. degree with at least 6 months of internship and/or graduate research experience
• Experience working with various biophysical instrumentation such as HPLC/UPLC (various detectors) and capillary electrophoresis (CE).
• Strong technical background on analytical methodologies using IP-RP, IEX, and AEX.
• 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 and LNP are a plus).
• Familiarity with applicable ICH regulations and multi-compendial guidelines related to method validation.
• Experience in assay development, qualification, validation, and transfer to GMP environments.
• Proven track record of success collaborating effectively with cross-functional teams.
• 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:_

• 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.

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
• Compensation: $33.00-$36.00 per hour based on education and experience

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