Scientist, Upstream Viral Vector

Summit Strategic Search•Philadelphia, PA
•$120,000 - $125,000•Onsite

About The Position

This is a lab-based scientist role on the upstream side of the client's viral vector group. You will own the cell culture experiments behind lentiviral vector production for next generation CAR-T work, and help grow the process from early stage culture into bioreactors. You will be the go-to person for how cells are grown, transfected, and fed, and your data will guide how the process is designed, compared, and handed off for further development.

Requirements

  • PhD plus at least 1 year in industry, or MS plus 4 or more years in industry, in cell biology, virology, chemical or biological engineering, or a similar discipline.
  • Hands-on experience growing mammalian cells in suspension to produce viral vector (lentiviral or AAV).
  • Hands-on experience with transient transfection.
  • Upstream experience in shake flasks and small bioreactors.
  • Solid molecular biology skills, including plasmid work and PCR, qPCR, or ddPCR assays.
  • A track record of designing experiments, troubleshooting when they fail, and drawing sound conclusions from the data.
  • Strong writing and presentation skills, with experience sharing results across functions.

Nice To Haves

  • Lentiviral vector production experience.
  • Experience taking a culture process into larger bioreactors.
  • Producer or packaging cell line development experience.
  • Industry experience in gene or cell therapy process development.

Responsibilities

  • Build and improve the upstream cell culture process, from early seed expansion through progressively larger bioreactor runs, with consistent results and a clear scientific basis for every process setting.
  • Run and refine lentiviral vector production, with a focus on transient transfection conditions; contribute to producer cell line work as programs require.
  • Improve titer, product quality, and consistency through media screening, feed design, and adjustments to culture conditions.
  • Plan targeted studies that show the process will hold up at larger scale.
  • Work hand in hand with colleagues in molecular biology, purification, analytics, and process development so each stage of the process fits together.
  • Help decide which early stage findings are ready to become formal process development work, and weigh in on study design and process comparability.
  • Work independently: set up your own experiments, run them, analyze the results, and decide what comes next.
  • Turn results into concise summaries, written reports, and presentations with clear recommendations for the wider team.
  • Work safely in a biosafety level 2 lab and keep complete, well organized electronic notebook records so every result can be traced and repeated.

Benefits

  • medical, dental, and vision coverage
  • a 401(k) with company match
  • paid parental leave
  • generous paid time off
  • Relocation assistance
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