Senior Scientist, Nucleic Acid Analysis & QC

Serif Biomedicines

Cambridge (MA)

Sur place

USD 126 000 - 182 000

Plein temps

Il y a 4 jours
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Résumé du poste

Serif Biomedicines in Cambridge, MA is seeking a Senior Scientist for Analytical Development and Quality Control. You will lead method development for nucleic acid therapeutics and LNP products, while mentoring junior colleagues in a fast-paced, entrepreneurial environment.

The role emphasizes hands-on bench work, rigorous data analysis, and collaboration across teams to support process development and regulatory submissions.

Qualifications

  • Degree in Chemistry, Biochemical Engineering, Biochemistry, Molecular Biology, Chemical Engineering, Biotechnology or related field.
  • B.S./M.S./Ph.D. with 5+ years (Ph.D.) or 12+ (M.S.) or 14+ (B.S.) of relevant industry experience.
  • Hands-on experience with mRNA/DNA cargo and LNP products.
  • Experience with HPLC/LC-MS and analytical method development.
  • Experience mentoring or guiding junior staff; strong written and oral communication.

Responsabilités

  • Lead method development and qualification for nucleic acid cargo and LNP product release, stability and characterization.
  • Lead experiments to optimize analytical methods for specificity, sensitivity, and accuracy.
  • Troubleshoot assay development and instrument issues; mentor junior team members.
  • Plan studies, schedule development projects, and support routine testing.
  • Provide technical input for regulatory filings and author protocols/reports.

Connaissances

Analytical method development
HPLC/LC-MS
Nucleic acid therapeutics
LNP delivery systems
Mentoring junior staff
Regulatory support writing

Formation

Relevant life sciences degree

Outils

Benchling
MS Office
JMP
GraphPad
Empower
Chromeleon

Description du poste

Serif Biomedicines in Cambridge, MA is seeking a Senior Scientist for Analytical Development and Quality Control. You will lead method development for nucleic acid therapeutics and LNP products, while mentoring junior colleagues in a fast-paced, entrepreneurial environment.

The role emphasizes hands-on bench work, rigorous data analysis, and collaboration across teams to support process development and regulatory submissions.

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