Bioanalytical Development Scientist - Viral Vectors

Position Overview

Our Eurofins PSS team is seeking an Analytical Development Scientist to work onsite supporting our client's analytical development activities across product characterization, process development, and analytical method execution for lentiviral vector (LVV)-based gene therapy products. The successful candidate will focus on routine analytical testing, data generation, and assay execution. The successful candidate will also contribute to analytical method development, optimization, and qualification activities with guidance from senior scientists. This role partners closely with cross-functional teams to generate analytical data that informs development decisions, process improvements, and regulatory submissions.

Responsibilities

• Execute analytical methods to support product characterization, process development, candidate selection, manufacturing support, and regulatory submissions.
• Perform routine testing and data analysis using analytical techniques such as plate-based bioassays with flow cytometry, qPCR, ddPCR, ELISA, and endotoxin methods.
• Assist with method development, optimization, qualification, and troubleshooting efforts aimed at improving assay performance, robustness, and reproducibility.
• Prepare and maintain analytical procedures, technical reports, protocols, and laboratory documentation in accordance with departmental standards.
• Collaborate with internal teams to share analytical results, help investigate technical issues, and support the rollout of analytical strategies across development programs.

Basic Minimum Qualifications

• B.S. in Biology, Biochemistry, Cell Biology, Molecular Biology or a related field with at least 1 year of relevant industry experience OR M.S. in Biology, Biochemistry, Cell Biology, Molecular Biology or a related field with 6 months of relevant industry experience.
• Hands-on experience with cell-based assays, including ELISA, MSD, Luminex and/or multi-color flow cytometry (3-5 color panels).
• Hands-on experience with molecular assays, including qPCR, RT-qPCR, PCR, and/or ddPCR.
• Familiar with mammalian cell culture handling and strong aseptic techniques.
• Experience documenting process results in electronic lab notebooks and effectively communicating experimental observations to management and cross-functional team.
• Meticulous attention to detail in sample tracking, experiment execution, data recording, and laboratory documentation.
• Ability to set priorities and multi-task activities to effectively manage workflows and drive deliverables to completion.
• Strong team orientation, with excellent organizational skills, self-motivation, and a positive attitude.
• Strong communication skills, with the ability to clearly communicate experimental results and observations.
• Authorization to work in the United States indefinitely without restriction or sponsorship.

Preferred Qualifications

• Previous experience with viral vector, cell therapy, gene therapy, or related biologics process development.
• Experience supporting development and optimization studies for method improvement efforts, including experimental design, data analysis, and documentation.
• Familiarity with assay qualification, validation, or method lifecycle support activities.
• Familiarity with automation platforms, liquid handlers, or high-throughput analytical workflows.