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 Associate (2nd Shift) as part of the Technical Operations team based in Raritan, NJ.
Role Overview
This position is responsible for performing manufacturing procedures and the execution of scheduled tasks within a CGMP environment. This position is responsible for quality and maintaining the highest standards in compliance within company policies, procedures, and all applicable regulations.
Key Responsibilities
- Be part of the manufacturing operations team responsible for production of autologous CAR-T products for clinical and commercial operation in a controlled current Good Manufacturing Practice (cGMP) cleanroom environment.
- Independently execute manufacturing or manufacturing-support processes according to standard operating procedures and current curriculum.
- Execute manufacturing activities common to cell culturing, purification, aseptic processing, and cryopreservation using appropriate techniques.
- Perform process unit operations according to standard operating procedures and batch records, and record production data and information in a clear, concise, format according to Good Documentation Practices (GDP).
- Perform tasks on time in a manner consistent with quality systems and cGMP requirements.
- Work in a team based, cross-functional environment to complete production tasks required by shift schedule.
- Aid in the development of manufacturing processes including appropriate documentation.
- Drive continuous improvement of manufacturing operations leveraging own observation as well as input of team members.
- Handle human derived materials in containment areas.
- Support schedule adjustments to meet production.
- Accurately complete documentation in SOP’s, logbooks and other GMP documents.
- Demonstrate training progression through assigned curriculum.
- Accountable for maintaining a working knowledge of basic cGMP requirements to ensure adherence to compliance policies and regulations
- Wear the appropriate PPE when working in manufacturing and other hazardous working environments.
- Proactively maintain a clean and safe work environment. Take necessary action to eliminate safety hazards and communicate to others any observed unsafe behaviors.
- Ensure materials are available for production.
- Job duties performed routinely require exposure to and handling of biological materials and hazardous chemicals
- Distance visual acuity of at least 20/40 (Snellen) in both eyes without corrective lenses or visual acuity corrected to 20/40 (Snellen) or better with corrective lenses.
- Color Perception both eyes 5 slides out of 8.
- Report to work on-time and according to the shift schedule.
- Perform other duties as assigned.
- Attend departmental and other scheduled meetings.
- Practice good interpersonal and communication skills.
- Demonstrate positive team-oriented approach in the daily execution of procedures.
- Promote and work within a team environment.
- Learn new skills, procedures and processes as assigned by management and continue to develop professionally.
- Support investigation efforts as required.
- Responsible for audit preparation and participation.
Requirements
- HS Diploma required with 3 – 5 Years Biotech/Pharmaceutical experience or equivalent industry experience // OR // Associates Degree required in Life Sciences or Manufacturing with 2 - 3 years of related experience // OR //Bachelors Degree required in Life Sciences with 0 - 2 years Biotech/Pharmaceutical experience or equivalent industry experience.
- Interpret a variety of instructions furnished in written, oral, diagram or schedule form.
- Follow instructions.
- Solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.
- Add, subtract, multiply and divide in all units of measure, using whole numbers, common factions, and decimals.
- Knowledge and ability to operate manufacturing, manufacturing-support and lab equipment.
- Knowledge of Process Excellence Tools
- Possesses solid knowledge of routine and non-routine testing and sampling methods, techniques and related equipment.
- Needs to be mobile and able to independently transport themselves between various sites/locations, as dictated by the essential functions and responsibilities of the position.
- Is frequently required to communicate with coworkers.
- While performing the duties of this job, the employee is regularly required to stand; walk; climb, bend and stoop; and reach with hands and arms.
- Ability to lift 25 lbs.
- Needs to perform gowning procedures to work in manufacturing core.
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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.
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.
Skills Required
- High School diploma with 3-5 years biotech/pharmaceutical experience OR Associate degree in Life Sciences/Manufacturing with 2-3 years related experience OR Bachelor's degree in Life Sciences with 0-2 years biotech/pharmaceutical experience
- Working knowledge of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP)
- Ability to perform aseptic processing, cell culture, purification, and cryopreservation techniques
- Experience operating manufacturing, manufacturing-support, and laboratory equipment
- Knowledge of Process Excellence Tools and continuous improvement principles
- Perform gowning procedures and work in controlled cleanroom environments (PPE compliance)
- Ability to accurately complete SOPs, logbooks, batch records, and other GMP documents
- Ability to handle human-derived biological materials and hazardous chemicals safely
- Physical requirements: stand/walk/climb/bend/stoop, reach, frequently communicate, and lift up to 25 lbs
- Vision requirements: distance visual acuity of at least 20/40 (with or without correction) and color perception 5 out of 8 slides
- Ability to report on time according to shift schedule and work 2nd shift onsite in Raritan, NJ
- Participate in audits, support investigations, attend meetings, and demonstrate training progression
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.
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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.
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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.
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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
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.
