Job Description

Role Summary

In this individual contributor role, you will play a critical part in ensuring the quality, integrity, and compliance of QC Chemistry activities supporting release and stability testing across our mRNA portfolio. You will combine deep analytical expertise with a strong quality mindset to review complex cGMP data, support laboratory operations, and continuously improve quality systems.


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Responsibilities
  • Perform cGMP Quality Control data review for QC Chemistry, including release and stability testing, while supporting Method Qualification and Acquisition activities as required.
  • Support method transfers and method development activities to ensure robust analytical capabilities.
  • Review executed assay packages in both paper and electronic formats, including chromatography data and other analytical outputs.
  • En...

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