Bioanalytical Development Scientist - Viral Vectors

Eurofins•Boston, MA

16h•$32 - $36•Onsite

About The Position

Eurofins Professional Scientific Services is seeking an Analytical Development Scientist to work onsite supporting a client's analytical development activities for lentiviral vector (LVV)-based gene therapy products. The role focuses on routine analytical testing, data generation, and assay execution, while contributing with guidance from senior scientists to analytical method development, optimization, and qualification. The scientist partners with cross-functional teams to generate analytical data that informs development decisions, process improvements, and regulatory submissions.

Requirements

Bachelor's degree in Biology, Biochemistry, Cell Biology, Molecular Biology, or a related field with at least 1 year of relevant industry experience, or a master's degree in one of these fields with at least 6 months of relevant industry experience.
Hands-on experience with cell-based assays, including ELISA, MSD, Luminex, and/or multicolor flow cytometry using 3–5 color panels.
Hands-on experience with molecular assays, including qPCR, RT-qPCR, PCR, and/or ddPCR.
Familiarity with mammalian cell culture handling and strong aseptic techniques.
Experience documenting process results in electronic lab notebooks and communicating experimental observations to management and cross-functional teams.
Meticulous attention to detail in sample tracking, experiment execution, data recording, and laboratory documentation.
Ability to set priorities and multitask to manage workflows and complete deliverables.
Strong team orientation, organizational skills, self-motivation, and a positive attitude.
Strong communication skills and the ability to clearly communicate experimental results and observations.
Authorization to work indefinitely in the United States without restriction or sponsorship.

Nice To Haves

Previous experience with viral vector, cell therapy, gene therapy, or related biologics process development.
Experience supporting method improvement studies, 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.

Responsibilities

Execute analytical methods supporting product characterization, process development, candidate selection, manufacturing support, and regulatory submissions.
Perform routine testing and data analysis using plate-based bioassays with flow cytometry, qPCR, ddPCR, ELISA, and endotoxin methods.
Assist with method development, optimization, qualification, and troubleshooting to improve 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.