Legend Biotech Corporation

Scientist

Legend Biotech Corporation$96K — $126K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • MS in Bioengineering, Virology, Cell Biology, Chemical Engineering, or related field with 4+ years experience; or PhD with 1 year industry experience.
  • Hands-on expertise in viral vector production and characterization.
  • Experience in mammalian suspension cell culture and upstream bioprocess development.
  • Strong knowledge of molecular biology techniques like plasmid construction and qPCR.
  • Proven ability to design and troubleshoot complex experiments in a fast-paced R&D environment.
  • Experience in scaling processes up to bioreactor systems (up to 50 L preferred).
  • Familiarity with gene therapy platform development, particularly lentiviral vectors.

Responsibilities

  • Define and optimize upstream process for vector production from shake flask to 40-L bioreactor.
  • Execute lentiviral vector production workflows for in-vivo CAR-T applications.
  • Conduct media optimization and feeding strategy development.
  • Develop scalable processes through fit-for-purpose studies.
  • Collaborate with internal teams to ensure effective technology transfer.
  • Provide technical input for experimental design and comparability strategies.
  • Independently plan, analyze, and report experiments with minimal guidance.

Benefits

  • Comprehensive medical, dental, and vision insurance.
  • 401(k) retirement plan with company match that vests on day one.
  • Eight weeks of paid parental leave after three months of employment.
  • Generous paid time off policy including vacation, personal days, and holidays.
  • Voluntary benefits like flexible spending accounts and life insurance.
  • Employee well-being initiatives including peer recognition programs.
Full Job Description
Scientist as part of the Research and Development team based in Philadelphia, PA.

Role Overview

Legend Biotech seeks 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.

Key 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.


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.


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The base pay range below is what Legend Biotech USA Inc. reasonably expects to offer at the time of posting. Actual compensation may vary based on experience, skills, qualifications, and geographic location. The company reserves the right to modify this range as needed and in accordance with applicable laws.

Other Types of Pay: Performance-based bonus and/or equity is available to employees in eligible roles.

Benefits and Paid Time Off: Medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer eight (8) weeks of paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and eleven (11) company holidays. Additional voluntary benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide voluntary commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.

Pay Range (Base Pay):

$96,267-$126,351 USD

Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech.

About Legend Biotech Corporation

Legend Biotech Corporation is a clinical-stage biopharmaceutical company focused on developing innovative cell therapies for cancer. The company's lead product candidate, LCAR-B38M/JNJ-68284528, is a chimeric antigen receptor (CAR) T-cell therapy that is being developed for the treatment of multiple myeloma, a type of blood cancer. Legend Biotech was founded in 2014 as a subsidiary of GenScript Biotech Corporation and became an independent company in 2019. The company is headquartered in Shanghai, China and has operations in the United States and Europe.
Learn more about Legend Biotech Corporation
Size
1,071 employees
Market Cap
$8.2 billion
Industry
NASDAQ

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