Scientist II, Analytical Development, Gene Editing and Molecular Assays

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life‑threatening diseases. Headquartered in Somerset, New Jersey, we develop advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T‑cell, T‑cell receptor (TCR‑T), and natural killer (NK) cell‑based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious, and cutting‑edge therapeutics for patients worldwide. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta‑cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a Scientist II, Analytical Development, Gene Editing and Molecular Assays as part of the Technical Development team based in Somerset, NJ . Role Overview This position will be responsible for developing analytical methods and performing QC and in‑process sample testing to support the manufacture and characterization of Legend’s gene and cellular therapy pipeline and first‑in‑human/new IND products. The individual will be responsible for analytical methods development, qualification, and internal or external transfer; routine testing of final product (GMP), stability, and in‑process samples; and performing data review and verification, lab and instrument maintenance, etc. The position will be responsible for maintaining accurate and contemporaneous records in a lab notebook and reporting results in a timely manner. Key Responsibilities Develop, optimize and qualify molecular biology methods for parameters such as VCN, gene editing proficiency, infectious titer, genomic titer, rapid mycoplasma, surrogate RCL, residual DNA, etc. Subject matter expert supporting routine testing of final product (GMP), stability, and in‑process. Perform review of testing data (e.g., data packets, final lot file, COA review). Perform data verification, data review and review of GMP documentation for multiple methods (general and complex) and/or products. Cross‑trained in multiple complex analytical methods and/or multiple products. Train others on multiple QC test methods, processes and procedures. Author and review/revise technical documents such as test methods, SOPs, specifications, trend reports and/or sample plans as appropriate. Maintain accurate and updated lab notebooks. Manage equipment and records for maintenance, calibration and operation. Contribute to maintenance of laboratory inventories. Procure and qualify required materials to perform experiments or testing. Work collaboratively with members of Analytical Development team to establish the analytical control strategy of the established methods. Perform other tasks as assigned. Typically, you have the authority to make decisions related to planning and execution of assay development runs. You can also make decisions related to weekly work priority. Higher‑level approvals are required for those related to significant assay development methodology changes, strategic shifts, or collaborations with other functional teams. Requirements BS, MS or Ph.D. in Molecular Biology, Cell Biology, Biochemistry, or a related field. A BS with 6‑8 years of significant practical experience; an MS with 4‑6 years of hands‑on experience in QC testing and method development and qualification of gene and cell therapy products, vaccine, antibody, AAV, other biologics; or a Ph.D. with 1‑3 years of assay development experience in the pharmaceutical field. Demonstrated experience in assay development and GMP QC testing of biologics (e.g., qPCR, dPCR, ddPCR, ELISA, cell culture and cell‑based assays). Ability to accurately and completely understand, follow, interpret and apply global regulatory and cGMP requirements. Ability to communicate effectively with peers, department management and cross‑functional peers about task status, roadblocks and needs. Advanced ability to work in a fast‑paced team environment, meet deadlines, and prioritize work from multiple projects. Advanced knowledge of LIMS, ELN, Veeva, GraphPad Prism, JMP and laboratory data analysis systems preferred. Expertise in analytical method qualification and validation, and tech transfer in in‑vivo CAR‑T, vaccine, antibody, AAV or other biologics is a plus. Strong communication skills, both written and verbal, with a demonstrated capacity to thrive in collaborative, team‑driven environments. Excel, Word, PowerPoint, etc. GraphPad Prism, other data analysis tools (PowerBI, JMP, etc). ELN, LabVantage, etc. Mandarin preferred. Pay Range (Base Pay)

$110,706 - $145,303 USD

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 weeks of paid parental leave after three months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and eleven 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, supplemental plans (pet, critical illness, accident, and hospital indemnity insurance), voluntary commuter benefits, family planning and care resources, well‑being initiatives, and peer‑to‑peer recognition programs. Work Authorization & Employment Eligibility Applicants must be authorized to work in the United States. As part of our commitment to maintaining a lawful workforce and ensuring compliance with federal employment regulations, we participate in the E‑Verify program. If you are selected for employment, you will be required to complete the Form I‑9 process, and your employment eligibility will be verified through E‑Verify in accordance with applicable federal law. We are committed to providing a fair, transparent, and welcoming hiring experience for all candidates. EEO Statement It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances. Employment is at‑will and may be terminated at any time with or without cause or notice by the employee or the company. For information related to our privacy notice, please review: Legend Biotech Privacy Notice. #J-18808-Ljbffr BioSpace