Biologics Formulation Scientist

Job description

Position Summary: Eurofins PSS is seeking a Formulation Scientist supporting high-throughput biologics formulation and analytical workflows in a development lab environment. Responsibilities include formulating proteins at high concentrations, executing stability studies, and performing analytical methods to measure conformational and colloidal stability. This is a temporary role expected to last around 12 months. Job Responsibilities: Execute protein-based developability and stability workflows, including formulation at high concentrations, viscometry, size exclusion chromatography, and assays for thermal and colloidal stability Execute workflows using automated high-throughput systems Independently support ongoing studies and high-level activities Apply scientific ownership and critical thinking to evaluate workflows and proactively communicate observations, risks, and process improvements Maintain accurate, compliant documentation within a method development environment Analyze data and report/communicate results May be expected to work with Antibody-Drug Conjugate (ADC) projects in Occupational Exposure Band 4 (OEB4) and/or OEB5, as well as other OEB4 materials Basic Minimum Qualifications Bachelor’s in a scientific discipline 2+ years of hands-on industry or research lab experience Authorization to work in the US without restrictions Preferred Qualifications Experience with buffer prep, high concentration antibody formulation via UFDF or TFF, protein handling, and assay execution Strong critical thinking, troubleshooting, and communication skills Experience with stability assays, including thermal or colloidal stability assessments Hands-on experience with analytical instrumentation such as SEC, HPLC, viscometry, rheology, DLS, DSC, DSF, or other related biophysical/analytical platforms Knowledge of protein chemistry and degradation Good time management and multi-tasking skills Effective communication and interpersonal skills, including ability to work within a cross-functional team Experience working in a method development or non-GMP development environment Exposure to automation or high-throughput workflows a plus