Sana Biotechnology

Scientist, Analytical Genomics

Sana Biotechnology$130K — $160K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • PhD in molecular biology, biochemistry, genomics, or related field with 2+ years of relevant industry experience or MS with 7+ years of relevant industry experience.
  • 4+ years of hands-on molecular biology experience, including nucleic acid extraction, quantification/QC, NGS library preparation, Illumina sequencing, ddPCR/RT-ddPCR, and qPCR.
  • Experience developing, optimizing, troubleshooting, and qualifying molecular or genomics assays for engineered cell and gene therapy products.
  • Experience with assay qualification, SOPs, regulatory-aligned documentation, and electronic systems such as Benchling or Veeva.
  • Ability to analyze, interpret, document, and communicate genomic assay results with various teams.

Responsibilities

  • Develop, optimize, and qualify molecular and genomics assays.
  • Apply genomic technologies and molecular workflows to assess editing and genomic integrity.
  • Develop reference materials and define assay controls and performance measures.
  • Execute core lab workflows including sample processing and sequencing.
  • Generate, review, analyze, and communicate genomic data with cross-functional partners.
  • Support method qualification and regulatory documentation for GxP activities.
  • Maintain Genomics Lab readiness and manage inventory and equipment.

Benefits

  • Collaborative team culture focused on patient outcomes.
  • Opportunity to work on innovative therapies for Type 1 Diabetes and CAR-T programs.
  • Engagement in cross-functional partnerships with computational biology and engineering.
  • Exposure to advanced genomic technologies and workflows.
  • Dynamic laboratory environment with emphasis on quality and regulatory compliance.
Full Job Description
About the role

As a lab-based Scientist, Analytical Genomics, you will report to the Director, Analytical Genomics to help advance Sana's Type 1 Diabetes and in vivo CAR-T programs by turning molecular and genomics assays into meaningful, decision-ready data. You will develop and execute assays that characterize engineered cell products, support method qualification and regulatory-aligned documentation, and keep the Genomics Lab ready to deliver high-quality results. You will also work closely with Computational Biology, Computational Engineering, and cross-functional partners to analyze and interpret genomic data that help move innovative therapies forward.

What you'll do
  • Develop, optimize, and qualify molecular and genomics assays to characterize engineered cell and gene therapy products.
  • Apply genomic technologies and molecular workflows, including on- and off-target editing assessment, genome integrity and stability assessment, single-cell and spatial transcriptomics, ddPCR, RT-ddPCR, and qPCR.
  • Develop reference materials and define assay controls, QC metrics, acceptance criteria, and performance measures.
  • Execute core laboratory workflows, including sample processing, nucleic acid extraction, library preparation, sequencing, and assay troubleshooting.
  • Generate, review, analyze, interpret and communicate genomic data with Computational Biology, Computational Engineering, and cross-functional partners to support Research, CMC, Clinical, and IND-enabling program decisions.
  • Support molecular and genomic method qualification, SOP development, and regulatory-aligned documentation for GxP activities and regulatory submissions.
  • Maintain accurate, traceable, and audit-ready records of sample tracking, metadata, experimental procedures, assay results, and study reports in Benchling and Veeva.
  • Maintain Genomics Lab readiness by supporting inventory control, equipment maintenance, reagent tracking, sample and material shipments, and CRO coordination.

What we're looking for
  • PhD in molecular biology, biochemistry, genomics, or related field with 2+ years of relevant industry experience, or MS with 7+ years of relevant industry experience.
  • 4+ years of hands-on molecular biology experience, including nucleic acid extraction, quantification/QC, NGS library preparation, Illumina sequencing, ddPCR/RT-ddPCR, and qPCR.
  • Experience developing, optimizing, troubleshooting, and qualifying molecular or genomics assays for engineered cell and gene therapy products.
  • Experience with assay qualification, SOPs, regulatory-aligned documentation, and electronic systems such as Benchling or Veeva.
  • Ability to analyze, interpret, document, and communicate genomic assay results with Computational, Research, CMC, Clinical, and program teams.

What will separate you from the crowd
  • Hands-on experience with on- and off-target editing assays, genomic integrity, and biodistribution that support cell and gene therapy programs.
  • Experience applying single-cell, spatial transcriptomics, multiomics or other advanced genomics workflows to answer complex biological or product-characterization questions.
  • Experience implementing automated sample preparation and assay execution platforms such as Hamilton, KingFisher, or similar systems.
  • Strong understanding of regulatory expectations for genomics assays, including analytical method qualification, GxP documentation, lab compliance, and IND-enabling support.
  • Ability to translate complex genomic assay data into clear, decision-ready summaries for Research, CMC, Clinical, and regulatory stakeholders.

What you should know
  • This role may require occasional evening or weekend work to support critical project deliverables.
  • The role includes standard laboratory activities such as standing, walking, sitting, using hands and arms, lifting or carrying up to 10 lbs, and occasional reaching, pushing, pulling, crouching, kneeling, twisting, or squatting.
  • The base pay range for this position at commencement of employment is expected to be between $130,000 and $160,00/year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience.


How we work together for patients
  • Lead from every seat - we seek to understand, act with honesty, and engage in the crucial conversations
  • Thrive as a team - we hire amazing people, are intensely curious, and cultivate inclusion and personal connectivity
  • Make it happen - we value vigorous debate, alignment around our decisions, and resilient execution

About Sana Biotechnology

Sana Biotechnology is a biotechnology company that develops and delivers engineered cells as medicines for patients. The company's platform allows for the rapid development of cell-based therapies that can be delivered directly to patients. Sana Biotechnology is focused on developing treatments for a range of diseases, including cancer, genetic disorders, and infectious diseases. The company was founded in 2018 by a group of experienced biotech executives and is headquartered in Seattle, Washington.
Learn more about Sana Biotechnology
Size
200 employees
Market Cap
$640.7 million
Industry
NASDAQ

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