Legend Biotech Corporation

Scientist I, Analytical Development

Legend Biotech Corporation$96K — $126K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree with 5+ years, Master's with 3-5 years, or PhD with 0-2 years of relevant experience.
  • Proven laboratory experience in flow cytometry, cell culture, ELISA, and cell-based assays.
  • Familiarity with compendial methods is preferred.
  • Knowledge of lentiviral vector characterization techniques.
  • Understanding of ICH guidelines for method qualification.
  • Experience in regulated environments for assay qualification and product testing.
  • Skills in document management and change approval processes.

Responsibilities

  • Develop and validate analytical methods for CAR-T and viral vector characterization.
  • Draft and review documentation including methods and protocols.
  • Manage laboratory inventory and order supplies as needed.
  • Create and assess materials required for analytical processes.
  • Adhere to safety standards and best practices in a laboratory setting.
  • Conduct qualifications, release testing, and characterization assessments.
  • Facilitate the transfer of methodologies among internal and external teams.

Benefits

  • Comprehensive medical, dental, and vision insurance.
  • 401(k) plan with company match that vests immediately.
  • Eight weeks of paid parental leave after three months of employment.
  • Robust paid time off policy including vacation and personal days.
  • Access to various voluntary benefits such as flexible spending accounts and life insurance.
Full Job Description
Scientist I, Analytical Development

Role Overview

We are seeking a dynamic and scientifically driven Scientist I to join Functional, Flow Cytometry and BioAnalytics team within our empowered Analytical Development organization. This role will focus on the establishment, development and qualification of analytical methods, including compendial methods, flow cytometry, cell-based potency, and immunoassays to support the development and manufacture of Legend's cell and gene therapy pipeline. This laboratory-focused role will require that candidates develop, optimize and execute analytical methods for product characterization, release and stability testing. This role will require authoring and reviewing documents, maintaining electronic laboratory notebooks, and contributing to cross-functional collaboration with other functional teams.

Key Responsibilities
  • Develop, optimize, and execute analytical methods to support viral vector and CAR-T product characterization, including compendial methods, titer, particle size, flow cytometry, and cell-based potency methods.
  • Author and review methods, protocols, and reports.
  • Maintain reagent inventory and order materials as laboratory activities require.
  • Generate and qualify critical materials for analytical methods.
  • Observe all laboratory safety standards including PPE use and BSL2 best practices.
  • Performing pre-qualification, assay qualification, product release testing, and product characterization testing in a quality control environment.
  • Technology transfer of methods to QC and external collaborators and receive methods from internal and external collaborators.
  • Maintain contemporaneous and accurate electronic laboratory records, including instrument maintenance records and sample inventory, following ALCOA+ standards.
  • Perform peer review and data integrity reviews in the analytical development and quality control environments.
  • Collaborate cross-functionally with PD, QC and Manufacturing teams to ensure seamless assay execution, troubleshooting, and continuous improvement.
  • Present scientific data at internal and external forums.
  • Balance multiple projects while meeting established timelines.
  • This role is empowered to make decisions related to day-to-day planning and execution of assay development runs according to timelines determined at the group level. Collaboration, consensus and alignment with management are required for decisions related to methodology, assay development strategy, or interactions with other functional teams.

Requirements
  • Bachelor's degree in a related field with 5 or more years of relevant experience, or Master's degree with 3 to 5 years of experience, or PhD with 0 to 2 years of experience.
  • Strong laboratory background, including experience with developing flow cytometry, mammalian cell culture, ELISA, and cell-based assays.
  • Experience implementing or executing compendial methods is preferred.
  • Experience with lentiviral vector characterization, including infectious titer, potency, and transduction efficacy assays.
  • Solid understanding of ICH guidelines and regulatory expectations for method qualification.
  • Experience with assay qualification, release testing and product characterization testing in a regulated environment.
  • Experience with document change management and document review/approval workflows is preferred.
  • Guide the establishing and authoring of SOPs/procedures for established methods
  • Detail-oriented with expertise in problem solving and solid decision-making abilities.
  • Excellent verbal and written communication skills.
  • Excel, Word, PowerPoint, etc.
  • GraphPad Prism, other data analysis tools (PowerBI, JUMP, R).
  • CytoExpert, FCS express, NovoExpress, FlowJo, etc.
  • ELN, LabVantage, etc.
  • Language(s): Strong written and verbal English skills are required. Mandarin preferred.

#Li-RP1

#Li-Onsite

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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