mRNA Analysis & Characterization Scientist

BioSpace

Waltham (MA)

On-site

USD 120,000 - 180,000

Full time

7 days ago
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Job summary

Sanofi Pasteur is seeking an mRNA Analytical Development Scientist to strengthen the Analytical Sciences group in R&D. The role focuses on developing and validating robust LC-MS based methods for mRNA vaccine characterization, supporting release and stability testing, and collaborating with CMC teams.

The candidate should have PhD or MSc with pharma/biotech analytical experience and a track record in method development and complex experiments, with strong writing skills for regulatory filings.

Qualifications

  • PhD or MSc with pharma/biotech analytical experience.
  • Experience in characterizing proteins, oligonucleotides, lipids and degradants via LC-MS.
  • Ability to develop and improve complex analytical methods.

Responsibilities

  • Develop advanced biochemical and biophysical assays, focusing on LC-MS characterization for mRNA vaccine process.
  • Collaborate with analytical leads to support CMC activities.
  • Write and review method documentation and characterization reports for regulatory filings.
  • Design and execute complex experiments independently, and report results.
  • Support QC and CRO investigations, deviations, and change control.
  • Train junior team members and promote lab safety and quality compliance.

Skills

LC-MS characterization
Analytical method development
Biochemical & biophysical assays
Team collaboration

Education

PhD in Analytical Chemistry / Biochemistry / Biotechnology
MSc in Analytical Chemistry / Biochemistry / Biotechnology

Tools

LC-MS instruments

Job description

Sanofi Pasteur is seeking an mRNA Analytical Development Scientist to strengthen the Analytical Sciences group in R&D. The role focuses on developing and validating robust LC-MS based methods for mRNA vaccine characterization, supporting release and stability testing, and collaborating with CMC teams.

The candidate should have PhD or MSc with pharma/biotech analytical experience and a track record in method development and complex experiments, with strong writing skills for regulatory filings.

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