$109,200 – $174,600
Listed on Moderna’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
Moderna is seeking a scientist to develop and optimize enzyme formulations for their DNA template manufacturing process, ensuring stability and performance across different storage and handling conditions. This role suits someone with strong protein formulation expertise who can translate manufacturing needs into practical formulation solutions through systematic testing and cross-functional collaboration.
Our summary, not Moderna’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- PhD in Pharmaceutical Sciences, Chemical Engineering, Biochemical Engineering, or related discipline; or MS with 5+ years of industry experience; or BS with 8+ years of industry experience
- Hands-on experience in protein, enzyme, biologics, or drug product formulation development
- Understanding of protein and enzyme stability mechanisms including aggregation, oxidation, deamidation, hydrolysis, and precipitation
- Experience designing and executing formulation screens, compatibility studies, and stability studies
- Experience using analytical or functional assays to characterize protein or enzyme formulations
- Ability to analyze data, troubleshoot technical issues, and recommend formulation changes
- Strong laboratory execution, documentation, and technical writing skills
- Cross-functional collaboration in development environments
- Must hold current US work authorization and be able to maintain it without sponsorship
Nice to have
- Experience with DNA or nucleic acid manufacturing enzymes such as polymerases, restriction enzymes, or nucleases
- Experience with DNA template production, plasmid DNA, or nucleic-acid-based platforms
- Experience developing liquid, frozen, refrigerated, or lyophilized formulations
- Experience with analytical methods such as enzyme activity assays, chromatography, DLS, DSC/DSF, osmolality, or particle analysis
- Experience with high-throughput screening, automation, or miniaturized scale-down models
- Experience preparing technical packages for technology transfer or regulatory documentation
- Familiarity with container-closure systems and material compatibility assessments
- Knowledge of GMP, GLP, or phase-appropriate development for biologics