Senior Research Associate, Analytical Development

If you’re interested in this role, please apply in English and include an English version of your Resume/CV. The Role In this role, you will support both analytical development and quality control for enzyme products used in meDNA synthesis. You will help advance and apply analytical methods to assess the performance and quality of enzyme cocktails and their component proteins, enabling scientifically rigorous evaluation and reliable product release. Through this work, you will contribute to ensuring that enzyme materials meet appropriate standards for research and clinical use, as applicable. Here’s What You’ll Do · Develop, establish, and improve analytical methods to evaluate the performance and quality of enzyme cocktails used in meDNA synthesis. · Develop and refine test methods for the component proteins within enzyme cocktails to enable objective and scientifically sound performance assessment. · Execute analytical testing and data analysis for enzyme products, component proteins, and samples generated by Process Development (PD) and Platform Technology & Industrialization (PTI) teams. · Generate analytical data to support method development, sample characterization, and technical decision-making across development programs. · Support quality control activities for enzyme products manufactured by Moderna Enzymatics, including testing to support product release and shipment decisions. · Prepare Statements of Analysis and related quality documentation for released materials. · Document experimental activities, analytical results, and supporting data in accordance with applicable procedures. · Collaborate with cross-functional partners across Analytical Development, PD , PTI, and other functions to support analytical strategy, quality evaluation, and shipment readiness. · Additional duties as may be assigned from time to time. Here’s What You’ll Need (Basic Qualifications) · Master’s degree or above in biochemistry, molecular biology, chemistry, biotechnology, or a related scientific discipline. · 2 years of industry experience in analytical testing, quality control, or a related function. · Hands-on experience with HPLC for analytical testing. · Hands-on experience in molecular biology and protein-related analytical testing. · Experience generating, analyzing, and documenting experimental data in a laboratory environment. · Ability to read scientific literature and technical protocols in English and communicate effectively in Japanese in a business setting. · Ability to work on-site at iPark Fujisawa, Japan. · At Moderna, we are focused on delivering on our mission by enabling talent to thrive. For this role, we are currently unable to offer immigration sponsorship. Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship. Here’s What You’ll Bring to the Table (Preferred Qualifications ) · Experience in the pharmaceutical or biotechnology industry, particularly in analytical or quality control roles. · Experience with LC-MS and other analytical techniques used for biomolecule characterization. · Experience in protein activity assays and characterization of enzyme products. · Hands-on experience with molecular biology techniques, including PCR, DNA cloning, E. coli culture and transformation, and plasmid DNA purification. · Experience using analytical instruments such as qPCR systems and plate readers for DNA, RNA, and enzyme analysis. · Experience with DNA sequence analysis workflows, including sample preparation and data analysis. · Experience working with small-volume samples and performing routine analytical work with a high degree of reproducibility. · Demonstrated ability to balance routine analytical responsibilities with research and development support. · Strong collaboration, communication, and problem-solving skills, with a proactive approach in a dynamic environment. · A desire to make an impact as part of a ... (truncated, view full listing at source)