Sr. Research Associate, Preclinical Quality Control in Research Analytics

The Role details the responsibilities of a highly skilled and motivated individual to support and advance high‑throughput pre‑clinical Quality Control (QC) workflows within Research Analytics. The role focuses on robust, reproducible analytical workflows for mRNA and Lipid Nanoparticle (LNP) materials, transitioning them from testing to release while collaborating with cross‑functional teams.

• Execute pre‑clinical QC analytical workflows to support testing of mRNA and encapsulated mRNA materials in a high‑throughput operations environment.
• Perform established analytical assays such as capillary electrophoresis, LC‑MS, HPLC/UPLC‑DLS, RT‑PCR, and other platform methods as applicable.
• Operate, maintain, and troubleshoot laboratory and automated testing equipment, including Hamilton liquid handling systems, liquid chromatography systems, plate readers, and other analytical instrumentation.
• Prepare samples, reagents, and assay materials to support high‑throughput testing workflows.
• Perform data analysis and documentation in accordance with internal procedures and data integrity expectations.
• Support assay troubleshooting, root‑cause evaluation, and workflow improvements to enhance method robustness, reproducibility, and data turnaround time.
• Track sample testing progress using various digital systems and provide timely updates to project and functional stakeholders.
• Support investigations, deviations, and technical assessments by compiling data, summarizing observations, and presenting findings clearly.
• Author, revise, and maintain documentation including Research Operating Procedures, data reports, and method execution records.
• Contribute to continuous improvement initiatives focused on assay throughput, operational efficiency, sample flow, equipment utilization, and data quality.
• Maintain safe laboratory practices and comply with company safety procedures, documentation standards, and quality expectations.
• Support general laboratory operations, including reagent preparation, inventory management, equipment maintenance, and coordination of supplies as needed.
• Demonstrate curiosity, accountability, and flexibility while working in a fast‑paced, matrixed environment with evolving priorities.

• B.S./B.A. with 2+ years of experience in Biochemistry, Molecular Biology, Bioanalytical Sciences, or related discipline (2–5+ years for B.S.; 0–3+ years for Master’s).
• Hands‑on experience executing analytical or bioanalytical assays in a quality‑focused, fast‑paced research/technical operations environment.
• Strong attention to detail and commitment to high‑quality documentation, data integrity, and reproducible execution.
• Ability to independently execute experiments or testing workflows while managing multiple priorities and timelines.
• Experience analyzing, interpreting, documenting, and communicating technical data.
• Demonstrated ability to troubleshoot laboratory methods, instrumentation, or workflow‑related issues.
• Strong interpersonal and collaborative skills, with the ability to work effectively across cross‑functional teams.
• Ability to operate with urgency, accountability, and transparency in a dynamic environment.

• M.S./M.A. with 2+ years of experience in Biochemistry, Molecular Biology, Bioanalytical Sciences, or related discipline.
• Expertise with high‑throughput analytical or automated liquid handling workflows.
• Hands‑on experience using Hamilton liquid handlers or other automated handling platforms.
• Familiarity with analytical platforms such as LC‑MS, HPLC/UPLC, RT‑PCR, sequencing‑based workflows, endotoxin testing.
• Experience supporting QC, Analytical Development or high‑throughput operations.
• Experience with sample management, plate‑based workflows and high‑volume testing execution.
• Demonstrated strength in project planning, prioritization, and stakeholder communication.
• Ability to identify workflow bottlenecks and propose practical improvements to increase efficiency, robustness, or scalability.
• Experience integrating automation or high‑throughput approaches into assay workflows.
• Strong written and verbal communication skills, including the ability to summarize…