Analytical Development Chemist

4w1 month ago

Eurofins

Boston, US · Full-time · $74,000 – $82,000

About this role

Eurofins is seeking a highly skilled, passionate, and motivated scientist to join our client Analytical Development team, supporting testing of non-GMP samples for development studies such as comparability assessments, process development, stability, and product and process characterization. This role focuses on 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.

In this role, you will provide testing support for a variety of purposes, including release and stability testing, product characterization, high-throughput analysis, and characterization of complex raw materials. You will collect, process, and analyze experimental data, ensuring accurate and timely documentation in an electronic laboratory notebook, and review, interpret, and present data within the analytical team and cross-functionally.

You will author, review, and revise technical source documents to support phase-appropriate comparability, and provide technical oversight to guide analytical/QC investigations as needed. The position requires active collaboration with internal and external process development and quality teams, along with training and mentoring junior team members as needed.

Eurofins Professional Scientific Services puts a focus on your professional growth, providing the ability to break into the biopharmaceutical industry and grow from the bottom up. We offer supportive teams and tools to invest in you while also affording you work-life balance and a competitive benefits package.

Requirements

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.
Demonstrated learning agility, scientific problem solving, and strong written and verbal communication skills.
Strong technical background on analytical methodologies using IP-RP, IEX, and AEX (preferred).

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.

Benefits

Professional growth focus with the ability to break into the biopharmaceutical industry and grow from the bottom up.
Supportive teams and tools to invest in your development.
Work-life balance.
Competitive benefits package.