Scientist / Senior Scientist, Analytical Development

Primary Responsibilities

• Drive the strategy, design, and execution of analytical characterization activities to support the development and advancement of RNA-based therapeutics and delivery platforms.
• Generate, interpret, and communicate scientific data that informs product understanding, process development, manufacturing readiness, and key development decisions.
• Advance organizational analytical capabilities by identifying, evaluating, and implementing innovative technologies, methodologies, and best practices.
• Collaborate across internal functions and external partners to deliver high-quality scientific outcomes, ensuring alignment with project objectives, timelines, and regulatory expectations.
• Provide technical leadership by mentoring scientists, fostering scientific excellence, maintaining thorough documentation, and contributing to regulatory and technical submissions.
• Monitor emerging scientific and industry trends to identify opportunities that strengthen technical expertise, accelerate innovation, and enhance the organization's analytical capabilities.

Qualifications

• Bachelor's, Master's, or Ph.D. in Chemistry, Biochemistry, Chemical Engineering, Molecular Biology, Pharmaceutical Sciences, or a related scientific discipline required.
• 6+ years of demonstrated working experience developing and applying analytical methods to support biologics, nucleic acid therapeutics, or other complex modalities, with expertise in chromatographic, spectrometric, and/or biophysical characterization techniques.
• Strong foundation in analytical method development, qualification, troubleshooting, and data interpretation within a research or drug development environment required.
• Hands-on laboratory experience with molecular biology, biochemical, and/or nucleic acid workflows, coupled with a solid understanding of experimental design and scientific problem solving.
• Proven ability to manage multiple priorities while maintaining documentation, producing high-quality technical reports, and contributing to regulatory or development documentation as appropriate.
• Knowledge of process development, analytical development, or CMC activities supporting RNA LNP therapeutics, biologics, or other advanced therapeutic platforms required.
• Ability to excel in a fast-paced, collaborative biotechnology environment, demonstrating adaptability, sound judgment, and a proactive approach to overcoming technical challenges.
• Excellent interpersonal, written, and verbal communication skills with a track record of collaborating across multidisciplinary teams while working both independently and as a technical leader.