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Lab Support Specialist

Somerset, New Jersey, United States

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life-threatening diseases. Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy through a portfolio of innovative technologies, including autologous, allogeneic, and in vivo cell therapy approaches. Our research spans chimeric antigen receptor T-cell (CAR-T), T-cell receptor (TCR-T), natural killer (NK) cell-based therapies, and other emerging platforms designed to transform the treatment of serious diseases. From our global network of research and development sites, we are committed to discovering and developing safe, effective, and cutting-edge therapies for patients worldwide.

Legend Biotech entered into a global collaboration agreement with Johnson & Johnson to jointly develop and commercialize CARVYKTI® (ciltacabtagene autoleucel; cilta-cel). Through this strategic partnership, we combine complementary expertise and capabilities to advance innovative immunotherapies for patients living with multiple myeloma.

Legend Biotech is seeking a Lab Support Specialist as part of the Research & Development team based in Somerset, NJ.

Role Overview

The Lab Support Specialist supports daily laboratory operations by managing samples, equipment, records, inventory, and supplies while assisting scientists and laboratory staff with testing activities. This role requires strong attention to detail, adherence to SOPs, safety/EHS, and regulatory requirements, and accurate documentation to maintain an audit-ready laboratory environment.

Key Responsibilities

  • Receive, process, track, and document samples in LIMS.
  • Maintain laboratory equipment, reagents, software, IT systems, and LIMS readiness.
  • Manage supplies, reagents, chemicals, ordering, and supply forecasting.
  • Support SOP compliance, audit readiness, EHS standards, and waste management.
  • Coordinate with Biosample Management, warehouse teams, scientists, and lab staff.
  • Support sample receipt, labeling, logging, processing, testing setup, chain of custody/identity, and LIMS documentation.
  • Coordinate with Biosample Management and warehouse teams for patient sample handling, shipments, inventory tracking, and documentation.
  • Operate, clean, calibrate, troubleshoot, and maintain laboratory equipment, reagents, software, IT systems, LIMS, and network setups.
  • Manage inventory of supplies, reagents, chemicals, and consumables; support ordering and forecasting to prevent operational delays.
  • Maintain an audit-ready laboratory by following SOPs and applicable quality, safety, EHS, and regulatory requirements.
  • Support safety protocols, chemical and biohazard waste management, lab cleanliness, organization, and biohazard control.
  • Assist scientists and laboratory staff with routine lab activities, reagent preparation, testing support, data recording, discrepancy reporting, and issue escalation.

Requirements

  • Associate or bachelor’s degree in biology, Chemistry, Medical Laboratory Science, or a related field preferred.
  • Previous laboratory or healthcare experience preferred.
  • Basic knowledge of laboratory procedures and safety practices.
  • Familiarity with LIMS and Microsoft Office preferred.
  • Ability to follow SOPs and safety regulations.
  • Strong teamwork and communication skills in a fast-paced environment.
  • Strong attention to detail, organization, and documentation accuracy.
  • Ability to follow SOPs, safety regulations, EHS guidelines, and regulatory requirements.
  • Accurate specimen handling, tracking, and recordkeeping.
  • Effective time management, multitasking, and prioritization.
  • Strong teamwork, collaboration, and written/verbal communication skills.
  • Basic computer, Microsoft Office, LIMS, and data entry skills.
  • Work in a clinical, research, pharmaceutical, or diagnostic laboratory.
  • May require standing for extended periods and lifting up to 25 pounds.
  • Use of personal protective equipment (PPE) is required.
  • May involve handling biological specimens and hazardous materials following safety guidelines.
  • Weekend work may be required, up to 10% of the time.

#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):

$63,298 - $83,077 USD

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

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.

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I (the candidate) enter into this Non-Disclosure Agreement (the “Agreement”) with Legend Biotech USA Inc. (the “Company”), effective as of the date of my acknowledgement below, for the purpose of enabling the Company to evaluate a possible employment relationship with me.

  1. Access to Company Confidential Information. I acknowledge that for the sole and limited purpose of evaluating a possible employment relationship with me, the Company might disclose, or enable me to have access to, certain Confidential Information of the Company, as defined below.  I agree that, except for purposes of evaluating a possible employment relationship with the Company or as expressly authorized in writing by the Company, I will (a) not use or disclose any Confidential Information; (b) keep all Confidential Information confidential at all times; and (c) not copy, reproduce or modify any Confidential Information.
  2. Definition of “Confidential Information.” For purposes of this Agreement, “Confidential Information” shall mean any and all information and materials provided to me by the Company, including without limitation, inventions, trade secrets, software code, product development and marketing strategies, ideas, processes, formulas, know-how, unpublished financial information, business plans, contractual relationships with third parties and operating strategies; memoranda, notes, records, drawings, manuals, disks, or other documents and media; and all embodiments, copies, extracts, and summaries thereof; provided, however, that “Confidential Information” shall not include information that: (a) is generally known or available to the public, or (b) is furnished to me by a third party who obtained such information using lawful means and without any restrictions on disclosure.
  3. Third Party Information. I agree that during the course of communications with the Company pursuant to this Agreement or in connection with my application and interviews for employment with the Company, I will not make any unauthorized use or disclosure to the Company of any confidential or proprietary information or trade secrets of any other person or entity to whom I have an obligation of confidentiality with respect to such information, including any current or former employer.  I further agree not to provide to the Company any materials or documents of any third party that are not generally available to the public.
  4. Remedies for Breach. I acknowledge that in the event of any breach of this Agreement, the Company will not have an adequate remedy in money or damages, and therefore the Company shall be entitled to obtain temporary, preliminary and/or permanent injunctive relief to redress any such breach, from any court of competent jurisdiction, and that the Company’s right to obtain such relief shall not limit its right to obtain other available remedies.
  5. General. The interpretation and enforcement of this Agreement shall be governed by the laws of the State of California.  This Agreement constitutes the entire agreement between the parties concerning the subject matters hereof; it supersedes any and all prior agreements or representations, written or oral, with respect to its subject matters; and it cannot be modified except in a written agreement signed by the Company.

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