Principal Research Associate, Analytical Development

Moderna Inc

Norwood, Massachusetts, United States
Base: $89,900.00 - $143,800.00; bonus/equity: elig...
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Bs/ms degree with relevant industry experience
Strong hands-on experience with cell-based bioassays
Experience with flow cytometry, elisa, hplc, or mass spectrometry
** Moderna Inc is seeking a Principal Research Associate in Analytical Development to enhance its mRNA science initiatives at their Norwood, Massachusetts location. The role involves bridging Analytical Development and Quality Control for bioassay operations, requiring strong technical expertise and collaboration skills. **

Job Summary

  • This role serves as a critical bridge between Analytical Development and Quality Control to ensure cell-based bioassays are robust and fully operational across development and commercial environments.
  • Candidates must possess deep technical expertise to translate development-stage methods into QC-ready assays while proactively addressing challenges related to transfer and lifecycle performance.
  • The position offers best-in-class healthcare coverage, family planning benefits, and a holistic approach to well-being within a culture that champions in-person collaboration.

Matching Summary

Match Score: 75

** Moderna Inc is seeking a Principal Research Associate in Analytical Development to enhance its mRNA science initiatives at their Norwood, Massachusetts location. The role involves bridging Analytical Development and Quality Control for bioassay operations, requiring strong technical expertise and collaboration skills. **

Salary

Base: $89,900.00 - $143,800.00; Bonus/Equity: Eligible for annual discretionary bonus and equity award; Benefits: Best-in-class healthcare, family planning, PTO, and savings opportunities

Skills & Requirements

Must-have

  • BS/MS degree with relevant industry experience
  • Strong hands-on experience with cell-based bioassays
  • Experience with flow cytometry, ELISA, HPLC, or mass spectrometry
  • Proven ability to troubleshoot complex assay issues in GMP environments
  • Understanding of CQA frameworks and regulatory expectations
  • 100% onsite work requirement in Norwood, Massachusetts

Nice-to-have

  • Experience leveraging Generative AI for assay optimization
  • Ability to translate technical concepts across functions
  • Self-motivated with a high degree of ownership mindset
  • Collaborative approach to cross-functional strategy discussions

Key Requirements

  • BS degree with ≥5 years or MS degree with ≥2 years experience
  • Must be eligible for export-controlled information (US person)
  • No immigration sponsorship available; US work authorization required

Work Rights

Must be a US person (citizen, permanent resident, asylee, or refugee) due to export control laws

Tailored Resume

Cover Letter