Process Lead Visa Sponsorship Jobs in New Jersey
Process lead visa sponsorship jobs in New Jersey are concentrated in the state's pharmaceutical, chemical, and consumer goods manufacturing sectors, with employers like Johnson & Johnson, Merck, and Honeywell filing sponsorship petitions across sites in Raritan, Rahway, and Morris Plains. Operations-focused multinationals in this corridor regularly sponsor international candidates for process lead roles.
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INTRODUCTION
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.
ROLE OVERVIEW
Legend Biotech is seeking a Manufacturing Lead Operator, Aseptic Process as part of the Manufacturing & Operations team based in Raritan, NJ. CAR-T products and processes are a novel cell therapy, and thus are well supported by a degree in engineering or a related field where not only are valuable scientific and technical skills learned, but also the ability to connect ideas and analyze complex problems. This role 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
- This individual establishes effective time management skills and prioritization of various job requirements, supported by a degree in engineering or related field to better analyze and execute effective decision during critical times for positive outcomes.
- To offer support in development of CAR-T manufacturing processes, this individual requires an understanding of the underlying technical requirements of the process and product must have, where complex risk analyses and change management techniques are utilized to establish a high quality and safe drug product through periods of improvement.
- This individual with strong scientific and technical background, will support the development of manufacturing processes, and will work with technical support and engineering personnel to drive continuous improvements and implement corrective and preventative actions within cell therapy Technical Operations.
- This individual will be responsible for general production floor oversight of Legend Biotech's BCMA CAR-T Cell Therapy Operations in both ISO 5 and ISO 7 environments, and support floor activities with extensive knowledge of CAR-T cell therapy processes, GMP quality systems and their regulatory requirements.
- This individual requires prior in-depth knowledge of lab sciences, cellular lab techniques, and data analysis to complete daily responsibilities and assess the impacts and consequences in relation to other process areas, without jeopardizing quality, accuracy and efficiency.
- This individual will perform process unit operations (i.e. cell culture, purification, aseptic processing, and cryopreservation) performed within specialized BSL2+ ISO 5 and ISO 7 cleanroom environments, according to standard operating procedures and batch records, while recording production data and information in a clear, concise format.
- This individual will require critical thinking and troubleshooting skills to respond to patient specific product issues to ensure continuous flow of operations, while performing tasks on time in a manner consistent with safety policies, quality systems, and cGMP requirements within particular manufacturing processes.
- Establish key stakeholder relationships with internal and external stakeholders, as collaboration and understanding across functional stakeholders are essential to maintaining this dynamic, fast-paced environment, which is CAR-T manufacturing.
- With a degree in engineering and related scientific or technical field, this individual must have the ability to interact with all levels within the organization through scientific and technical expertise.
- Strong communicative skills and a broad technical understanding of complex systems are must haves, to build strong partnerships with Manufacturing, Engineering, and Quality, and work as part of a cross-functional and matrixed team to successfully manufacture CAR-T product in a safe and high quality manner.
REQUIREMENTS
- Bachelor's degree in life science/engineering, or related field or equivalent experience required.
- A minimum of 2 years of operations experience within a cGMP environment in the biotech/biopharma industry. Prior experience in manufacturing, maintenance, quality, testing, or engineering is required. Prior experience in an aseptic manufacturing environment is preferred.
- 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.
- 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.
- AI Literacy: Possesses a working knowledge of AI technologies and approved AI tools, applies them responsibly to enhance productivity and decision-making, exercises appropriate human oversight of AI-generated outputs, and complies with organizational policies governing AI use.
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.
Process Lead Job Roles in New Jersey
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Search Process Lead Jobs in New JerseyProcess Lead Jobs in New Jersey: Frequently Asked Questions
Which companies sponsor visas for process leads in New Jersey?
New Jersey's pharmaceutical and specialty chemicals industries are the most active sponsors for process lead roles. Companies like Johnson & Johnson, Merck, BASF, and Honeywell have documented histories of sponsoring operations and manufacturing professionals at New Jersey facilities. Consumer goods manufacturers in the central and northern parts of the state also appear in DOL sponsorship filings for process-level operations roles.
Which visa types realistically fit process lead roles in New Jersey?
Process lead roles are typically classified as operations or manufacturing management positions. If the employer requires a bachelor's degree in a directly related field such as chemical engineering, industrial engineering, or operations management, the role may qualify as a specialty occupation under the H-1B visa. Employers file a Labor Condition Application and then an I-129 petition with USCIS. Australian nationals may pursue the E-3 visa on the same specialty occupation basis. EB-2 and EB-3 employment-based green cards are available for longer-term sponsorship paths, with EB-3 covering skilled workers with at least two years of experience.
Which cities in New Jersey have the most process lead sponsorship jobs?
The highest concentration of sponsored process lead roles in New Jersey is found along the Route 1 and I-287 pharmaceutical corridor, particularly in Raritan, Rahway, Parsippany, and Bridgewater. These towns host major manufacturing and operations campuses for life sciences and specialty chemicals firms. Edison and Somerset also appear frequently in DOL sponsorship filings, reflecting the density of chemical and consumer goods manufacturing in central New Jersey.
How to find process lead visa sponsorship jobs in New Jersey?
Migrate Mate lists New Jersey employers with verified sponsorship histories for process lead and operations roles, searchable by city and employer. Because process lead sponsorship depends heavily on the specific degree requirement an employer attaches to the role, focusing on companies with prior H-1B or EB-3 filings in manufacturing and operations gives you the strongest starting point. Migrate Mate surfaces this filing history so you can target employers already familiar with the sponsorship process.
Are there state-specific factors that affect process lead sponsorship in New Jersey?
New Jersey's dense concentration of FDA-regulated pharmaceutical and biotech manufacturers means process lead roles frequently carry formal degree requirements in engineering or life sciences, which strengthens the specialty occupation argument for H-1B sponsorship. The state's proximity to major research universities also means employers in this corridor have established international hiring pipelines. However, sponsorship is not automatic, and each employer evaluates the role independently before committing to file a petition.
What is the prevailing wage for sponsored process lead jobs in New Jersey?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.