Operations Support Specialist

Posted 13 Days Ago
Be an Early Applicant
Raritan, NJ, USA
In-Office
48K-63K Annually
Entry level
Biotech
The Role
Supports production of personalized CAR-T cell therapies in a sterile cGMP environment. Performs cell culture, purification, aseptic processing, and cryopreservation according to procedures and batch records. Records production data, follows safety and quality requirements, collaborates with Manufacturing, Engineering, and Quality, and contributes to process development and continuous improvement. The role requires shift work, handling biological materials and hazardous chemicals, physical dexterity, lifting up to 50 pounds, prolonged standing, and occasional unplanned overtime.
Summary Generated by Built In

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 an Operations Support Specialist 1st Shift (Sun-Wed) as part of the Technical Operations team based in Raritan, NJ.

Role Overview

The CAR-T Operations Support Specialist will be part of the Technical Operations team responsible for the production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment. Job duties will be performed within a team based on an assigned production shift schedule.

Key Responsibilities

  • Perform process unit operations (i.e. cell culture, purification, aseptic processing, and cryopreservation) according to standard operating procedures and batch records, while recording production data and information in a clear, concise format.
  • Perform tasks on time in a manner consistent with safety policies, quality systems, and cGMP requirements.
  • Build strong partnerships with Manufacturing, Engineering, and Quality, and work as part of a cross-functional team to complete production tasks required by shift schedule.
  • Support the development of manufacturing processes, and will work with others to drive continuous improvements and efficiencies within cell therapy Technical Operations.
  • Job duties performed routinely require exposure to and handling of biological materials and hazardous chemicals. 
  • Ability to interact with all levels within the organization.

Requirements

  • Bachelor’s degree in engineering or related field or equivalent experience required.
  • A minimum of 0-1 years of operations experience within a cGMP environment in the biotech/biopharma industry.
  • An ability to build strong partnerships and effectively integrate with external collaborators to drive projects/programs forward in a matrixed environment.
  • Ability to work independently and successfully, prioritize and manage multiple tasks simultaneously, integrate cross-functional issues and balance competing priorities effectively.
  • Clear and succinct verbal and written communication skills with an attention to detail and the ability to follow procedures.
  • Knowledge of cGMP regulations and FDA guidance related to manufacturing of cell based products.
  • Ability to lift a minimum of 50 lbs and stand for a long period of time.
  • Sufficient vision and hearing capability to work in job environment with physical dexterity sufficient to use computers and document production records.
  • Ability to handle human derived materials in BSL-2 cleanroom facility.
  • Physical dexterity sufficient to use computers and documentation.
  • Ability to accommodate shift work including evenings and weekends as required by the manufacturing process.
  • Ability to accommodate unplanned overtime on little to no prior notice.

#Li-RN1

#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):
$47,861$62,819 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.

Skills Required

  • Bachelor's degree in engineering or a related field, or equivalent experience
  • 0–1 years of operations experience in a cGMP biotech or biopharma environment
  • Ability to build partnerships and integrate with external collaborators in a matrixed environment
  • Ability to work independently, prioritize multiple tasks, manage competing priorities, and address cross-functional issues
  • Clear verbal and written communication skills, attention to detail, and ability to follow procedures
  • Knowledge of cGMP regulations and FDA guidance for manufacturing cell-based products
  • Ability to lift at least 50 pounds and stand for extended periods
  • Vision, hearing, and physical dexterity sufficient for the work environment and computer use
  • Ability to handle human-derived materials in a BSL-2 cleanroom facility
  • Ability to work assigned shifts, including evenings and weekends
  • Ability to work unplanned overtime with little or no advance notice

Legend Biotech Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Legend Biotech and has not been reviewed or approved by Legend Biotech.

  • Fair & Transparent Compensation Pay is considered competitive for many roles, with base rates often described as good or above local industry averages. Feedback suggests posted figures for titles like Specialist, Scientist, and certain HR roles sit above common national benchmarks.
  • Retirement Support A 401(k) company match that vests on day one is repeatedly highlighted as a standout element. Immediate vesting increases the tangible value of the retirement offering from the start of employment.
  • Leave & Time Off Breadth PTO structures commonly include vacation, personal, sick time, floating holidays, and around 11 company holidays. Several postings outline clear day allocations, signaling breadth and clarity in time-off design.

Legend Biotech Insights

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The Company
HQ: Somerset, New Jersey
1,192 Employees
Year Founded: 2014

What We Do

Legend Biotech is a global, commercial-stage biotechnology company developing and manufacturing novel therapies. We explore and apply innovative technologies to deliver cutting-edge options for patients around the world. Our corporate headquarters is located in Somerset, NJ, and our manufacturing footprint includes facilities in the United States, China and the Belgium.

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