asimov

Senior Scientist, Lentiviral Vector Cell Line Development

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Posted within 60 days ·

  • onsite
  • FullTime
  • Synthetic Biology
  • Boston, MA
Work arrangement
onsite
Employment
FullTime
Stated compensation
USD 145,000–165,000 1 YEAR
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Requirements

2 with evidence7 unclear or unstated
Remote policy
onsite
“Provider workplace type: onsite”
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Minimum experience (years)
7
“7+ years of hands-on experience in biopharma, including 4+ years focused on lentiviral vector producer or packaging cell line development in support of GLP or GMP production of cell or gene therapies.”
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Employment type
FullTime
Compensation
USD 145,000–165,000 1 YEAR
7 fields not stated in this posting
Employer sponsorship
Not specified
Geographic scope
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Degree requirement
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Security clearance
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READ IT IN THE EMPLOYER’S OWN WORDS

Original job description

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Our mission at Asimov is to advance humanity's ability to design living systems, enabling biotechnologies with outsized benefit to society. We are developing a mammalian synthetic biology platform––from cells to software––to enable the design and manufacture of next-generation therapeutics. We are hiring a Senior Scientist to lead our Lentiviral Vector Cell Line Development team in Boston, MA. This role blends strategic leadership with hands-on experimentation, giving you direct influence over our Lentiviral Vector platform roadmap and scientific vision. You will drive the creation of stable producer cell lines for lentiviral vector therapeutics while innovating next-generation cell line development workflows. This is a unique opportunity to work at a nimble, forward-thinking synthetic biology startup and help build the future of biological engineering. About the Role:
Read full descriptionShow less description
Set and steer the scientific roadmap for the Lentiviral Vector cell line development (CLD) platform. Perform lentiviral vector stable producer cell line development processes including transfection, pool generation, single cell cloning, clone screening and characterization, and cell banking using state-of-the-art equipment. Serve as the primary Lentiviral Vector CLD technical contact on customer and commercial projects. Partner with our commercial team to present platform capabilities to prospective partners and translate customer requirements into executable CLD project plans. Provide technical leadership and mentorship to scientists on the team, including managing direct report(s) and setting a high bar for experimental design, data analysis and record-keeping. Represent Lentiviral Vector CLD on cross-functional and leadership-facing project teams, making calls on cell line development strategy and clearly communicating progress, risk and plans. Support innovation through development of novel workflows and applications Support research projects to develop viral vector production methods to enhance product quality attributes such as empty/full ratio, potency and/or cell targeting. Work effectively as part of a cross-functional team in support of a Lentiviral Vector CLD platform and in collaboration with Synthetic Biology and Process Development teams. Design experiments, analyze data, troubleshoot, and maintain detailed records. Represent Lentiviral Vector CLD on project teams, making decisions for cell line development activities and effectively communicating results, progress and plans. Represent Asimov's science externally through publications and presentations at leading industry conferences. About You: M.S. or PhD in Biological Engineering, Virology, Cell Biology, Molecular Biology, or a related field. 7+ years of hands-on experience in biopharma, including 4+ years focused on lentiviral vector producer or packaging cell line development in support of GLP or GMP production of cell or gene therapies. 2+ years of experience managing direct report(s) and providing technical guidance. Proven track record balancing hands-on bench leadership with big-picture platform strategy and roadmapping. Experience communicating technical work to external stakeholders and translating their needs into technical plans. Demonstrated ability to communicate scientific work externally, evidenced by publications, patents, and/or conference presentations. Experience with downstream purification and PQ assessment of lentiviral vectors, T-cell transduction assay, viral genome engineering, and/or host cell genome engineering related to virus production or producer cell line technologies is highly desired. Experience with process development at Ambr or benchtop bioreactor scale is a plus. Comfortable working with large, multidimensional datasets and applying statistical or computational methods to extract actionable biological or process insights. Strong written and verbal communication skills required. We're fueled by a vision to transform biological engineering into a fully-fledged engineering discipline. Should you join our team, you will grow with a constantly evolving organization and push the frontiers of synthetic biology. Company culture is key to Asimov, and ours is a culture of recombination; we believe that our mission can only be achieved by bringing together a diverse team with a mixture of backgrounds and perspectives.
Original formatting and links

Our mission at Asimov is to advance humanity's ability to design living systems, enabling biotechnologies with outsized benefit to society. We are developing a mammalian synthetic biology platform––from cells to software––to enable the design and manufacture of next-generation therapeutics.

We are hiring a Senior Scientist to lead our Lentiviral Vector Cell Line Development team in Boston, MA. This role blends strategic leadership with hands-on experimentation, giving you direct influence over our Lentiviral Vector platform roadmap and scientific vision. You will drive the creation of stable producer cell lines for lentiviral vector therapeutics while innovating next-generation cell line development workflows. This is a unique opportunity to work at a nimble, forward-thinking synthetic biology startup and help build the future of biological engineering.


About the Role:

  • Set and steer the scientific roadmap for the Lentiviral Vector cell line development (CLD) platform.

  • Perform lentiviral vector stable producer cell line development processes including transfection, pool generation, single cell cloning, clone screening and characterization, and cell banking using state-of-the-art equipment.

  • Serve as the primary Lentiviral Vector CLD technical contact on customer and commercial projects. Partner with our commercial team to present platform capabilities to prospective partners and translate customer requirements into executable CLD project plans.

  • Provide technical leadership and mentorship to scientists on the team, including managing direct report(s) and setting a high bar for experimental design, data analysis and record-keeping.

  • Represent Lentiviral Vector CLD on cross-functional and leadership-facing project teams, making calls on cell line development strategy and clearly communicating progress, risk and plans.

  • Support innovation through development of novel workflows and applications

  • Support research projects to develop viral vector production methods to enhance product quality attributes such as empty/full ratio, potency and/or cell targeting.

  • Work effectively as part of a cross-functional team in support of a Lentiviral Vector CLD platform and in collaboration with Synthetic Biology and Process Development teams.

  • Design experiments, analyze data, troubleshoot, and maintain detailed records.

  • Represent Lentiviral Vector CLD on project teams, making decisions for cell line development activities and effectively communicating results, progress and plans.

  • Represent Asimov's science externally through publications and presentations at leading industry conferences.


About You:

  • M.S. or PhD in Biological Engineering, Virology, Cell Biology, Molecular Biology, or a related field.

  • 7+ years of hands-on experience in biopharma, including 4+ years focused on lentiviral vector producer or packaging cell line development in support of GLP or GMP production of cell or gene therapies.

  • 2+ years of experience managing direct report(s) and providing technical guidance.

  • Proven track record balancing hands-on bench leadership with big-picture platform strategy and roadmapping.

  • Experience communicating technical work to external stakeholders and translating their needs into technical plans.

  • Demonstrated ability to communicate scientific work externally, evidenced by publications, patents, and/or conference presentations.

  • Experience with downstream purification and PQ assessment of lentiviral vectors, T-cell transduction assay, viral genome engineering, and/or host cell genome engineering related to virus production or producer cell line technologies is highly desired.

  • Experience with process development at Ambr or benchtop bioreactor scale is a plus.

  • Comfortable working with large, multidimensional datasets and applying statistical or computational methods to extract actionable biological or process insights.

  • Strong written and verbal communication skills required.

We're fueled by a vision to transform biological engineering into a fully-fledged engineering discipline. Should you join our team, you will grow with a constantly evolving organization and push the frontiers of synthetic biology. Company culture is key to Asimov, and ours is a culture of recombination; we believe that our mission can only be achieved by bringing together a diverse team with a mixture of backgrounds and perspectives.

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