Scientist

Legend Biotech USPhiladelphia, PA
$96,267 - $126,351Onsite

About The Position

Legend Biotech is seeking an experienced Scientist to join the Upstream team, Vector Biology in Philadelphia, with a focus on in-vivo CAR-T programs. This independent contributor role will own hands-on execution and data-driven development of lentiviral vector upstream processes, including seed train strategy and scale-up from small-scale to 40-Liter bioreactor runs. This Scientist position will closely work with Molecular Biology, Downstream, Analytical and Technical development partners to ensure end-to-end process alignment, support comparability strategy and readiness, and enable efficient, high-quality technology transfer.

Requirements

  • MS degree with 4+ years; or PhD degree with 1 year’s prior industry experience in Bioengineering, Virology, Cell biology, Chemical Engineering, or related field.
  • Hands-on experience in viral vector production, and characterization.
  • Experience with mammalian suspension cell culture, transient transfection, and upstream bioprocess development.
  • Strong technical background in molecular biology techniques, including plasmid construction, PCR/qPCR/dPCR based assay, and cell line development.
  • Demonstrated ability to design, execute, analyze, and troubleshoot complex experiments in a fast-paced R&D environment.
  • Experience scaling upstream processes from shake flasks to bioreactor system (up to 50 L preferred).
  • Experience supporting gene therapy platform development, preferably involving lentiviral vector applications.
  • Basic understanding of upstream process development and their impact on product quality.
  • Strong organizational and time management skills, with the ability to manage multiple projects and priorities.
  • Excellent analytical and problem-solving skills with the ability to interpret data and recommend next steps.
  • Proficiency in maintaining accurate experimental records and documenting data using electronic laboratory notebooks (ELNs) to ensure data traceability.
  • Excellent verbal and written communication skills, with experience preparing technical reports and presenting scientific findings to cross-functional teams.
  • Ability to work both independently and collaboratively in a multidisciplinary research environment.
  • Adaptable, self-motivated, and eager to learn new technologies and experimental approaches.

Responsibilities

  • Define and optimize the upstream process from shake flask through bioreactors, scaling to 40-L with reproducible performance and clear rational for operating parameters.
  • Execute and optimize lentiviral vector production workflows supporting in-vivo CAR-T application, including transient transfection optimization and/or stable cell line optimization.
  • Perform media optimization, feeding strategy development, and process control adjustments to improve yield, quality, scalability and robustness.
  • Develop and execute fit-for-purpose studies to support scalability and readiness.
  • Collaborate with internal teams within Vector Biology and coordinate cross-functional activities to support technology transfer to internal Technical Development team.
  • Contribute technical input to cross-functional discussions on experimental design, comparability strategy, and progression of exploratory work into formal process development.
  • Independently plan, perform, analyze, and interpret experiments with minimal supervision.
  • Deliver clear data summaries and evidence-based recommendations to Vector Biology and cross-functional teams.
  • Prepare high-quality technical reports, study summaries, and slide decks to support decisions on the upstream process development.
  • Adhere to BSL-2 biosafety standards and Legend policies, maintaining accurate and compliant electronic lab notebooks and documentation.
  • Ensure experimental reproducibility and data integrity through detailed and organized record-keeping.

Benefits

  • Medical, dental, and vision insurance
  • 401(k) retirement plan with a company match that vests fully on day one
  • Eight (8) weeks of paid parental leave after just three (3) months of employment
  • Paid time off policy that includes vacation time, personal time, sick time, floating holidays, and eleven (11) company holidays
  • Flexible spending and health savings accounts
  • Life and AD&D insurance
  • Short- and long-term disability coverage
  • Legal assistance
  • Supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance
  • Voluntary commuter benefits
  • Family planning and care resources
  • Well-being initiatives
  • Peer-to-peer recognition programs
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