Molecular Biology Scientist — ddPCR/qPCR & Analytics

CHEManager International

San Diego (CA)

Vor Ort

USD 110.000 - 135.000

Vollzeit

vor 24 Stunden
Sei unter den ersten Bewerbenden
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Zusammenfassung

Kenai Therapeutics in San Diego is seeking a Scientist to join Analytical Development to develop, optimize and validate molecular biology methods across development stages. The role requires hands-on assay design for ddPCR/qPCR, data analysis, instrument maintenance and strong documentation practices.

Collaborate with CMC, Process Development and Quality to ensure analytical readiness for clinical milestones. Excellent writing and communication are essential in a fast-paced biotech environment.

Qualifikationen

  • Analytical development experience in molecular biology assays.
  • Experience with ddPCR/qPCR and data interpretation.
  • Strong technical writing and reporting skills.

Aufgaben

  • Lead assay design, development and qualification/validation of molecular biology assays.
  • Plan, troubleshoot and execute lab activities including instrument setup and data analysis.
  • Maintain cell lines/banks used in assay development.
  • Design robustness studies per regulatory guidelines.
  • Generate and present data in cross-functional meetings.
  • Prepare reports, SOPs and technical documents.
  • Support method transfers and validation in GMP environments.

Kenntnisse

Analytical development
Molecular biology assays
PCR/data analysis
Cell culture handling
Statistical analysis (JMP/Prism)
Technical writing
Communication skills

Ausbildung

Ph.D. in Immunology, Cell Biology, Neuroscience or related field
MS in related field

Tools

Qiagen instruments
ThermoFisher instruments
Bio-Rad instruments
QuantStudio
QX Manager
Quantasoft
JMP
GraphPad Prism

Jobbeschreibung

Kenai Therapeutics in San Diego is seeking a Scientist to join Analytical Development to develop, optimize and validate molecular biology methods across development stages. The role requires hands-on assay design for ddPCR/qPCR, data analysis, instrument maintenance and strong documentation practices.

Collaborate with CMC, Process Development and Quality to ensure analytical readiness for clinical milestones. Excellent writing and communication are essential in a fast-paced biotech environment.

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