Biotech & Pharma CPT Jobs in New Jersey
New Jersey is one of the country's most active biotech and pharma hubs, home to major employers like Johnson & Johnson, Merck, Becton Dickinson, and Bristol Myers Squibb. F-1 students pursuing CPT can find research, lab, and clinical development roles across the Princeton Corridor, Parsippany, and the Raritan Valley, where dense industry clusters support structured internship and co-op programs.
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Get Access To All JobsINTRODUCTION
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 QC Stability Coordinator as part of the Technical Development team based in Somerset, NJ. This role provides hands-on experience in laboratory operations, stability data trending, documentation, and compliance with regulatory guidelines.
KEY RESPONSIBILITIES
- Oversee the scheduling, pulling, and testing of stability samples across internal and external QC labs.
- Maintain accurate and contemporaneous records in Quality Management Systems and in a verified database for internal stakeholders.
- Conduct stability trending analysis from analytical results for review by QC manager or SME. Assist in preparing charts, graphs, and preliminary reports and be able to deliver within the targeted timeline.
- Participate in team meetings and provide updates on assigned tasks.
REQUIREMENTS
- Currently enrolled in a U.S. college or university program (Chemistry, Biology, Pharmaceutical Sciences, or related field).
- Someone in their Sophomore or Junior year preferred.
- Basic understanding of laboratory procedures and scientific data handling.
- Motivated, highly organized, strong attention to detail and multi-tasking skills.
- Proficiency in Microsoft Excel and/or SMARTSHEET. Power BI as a plus.
- Excellent written and verbal communication skills. Ability to work independently and as part of a team.
- Hybrid onsite schedule, at least 3 days a week on Mon, Tue and Thu.
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.
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 QC Stability Coordinator as part of the Technical Development team based in Somerset, NJ. This role provides hands-on experience in laboratory operations, stability data trending, documentation, and compliance with regulatory guidelines.
KEY RESPONSIBILITIES
- Oversee the scheduling, pulling, and testing of stability samples across internal and external QC labs.
- Maintain accurate and contemporaneous records in Quality Management Systems and in a verified database for internal stakeholders.
- Conduct stability trending analysis from analytical results for review by QC manager or SME. Assist in preparing charts, graphs, and preliminary reports and be able to deliver within the targeted timeline.
- Participate in team meetings and provide updates on assigned tasks.
REQUIREMENTS
- Currently enrolled in a U.S. college or university program (Chemistry, Biology, Pharmaceutical Sciences, or related field).
- Someone in their Sophomore or Junior year preferred.
- Basic understanding of laboratory procedures and scientific data handling.
- Motivated, highly organized, strong attention to detail and multi-tasking skills.
- Proficiency in Microsoft Excel and/or SMARTSHEET. Power BI as a plus.
- Excellent written and verbal communication skills. Ability to work independently and as part of a team.
- Hybrid onsite schedule, at least 3 days a week on Mon, Tue and Thu.
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.
CPT Biotech & Pharma Job Roles in New Jersey
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Search Biotech & Pharma Jobs in New JerseyBiotech & Pharma CPT Sponsorship Jobs in New Jersey: Frequently Asked Questions
Which biotech & pharma companies sponsor F-1 CPT visas in New Jersey?
New Jersey hosts a high concentration of biotech and pharma employers with established CPT programs. Johnson & Johnson in New Brunswick, Merck in Rahway, Becton Dickinson in Franklin Lakes, and Bristol Myers Squibb in Lawrenceville have historically taken on F-1 CPT interns and co-op students. Smaller contract research organizations and biotech startups throughout the Princeton Corridor also participate, though CPT eligibility ultimately depends on your school's authorization and the employer's willingness to coordinate with your DSO.
Which cities in New Jersey have the most biotech & pharma F-1 CPT sponsorship jobs?
The greatest concentration of biotech and pharma CPT opportunities in New Jersey falls along the Route 1 corridor between Princeton and New Brunswick, as well as in Rahway, Parsippany, and Morris County. Parsippany and the surrounding Morristown area have a dense cluster of pharmaceutical and life sciences offices. For students at Rutgers or nearby universities, on-site roles in New Brunswick and Piscataway are particularly accessible given proximity to campus research infrastructure.
What types of biotech & pharma roles typically qualify for F-1 CPT sponsorship?
Roles that are directly tied to a student's field of study and structured as part of a degree program are the ones most commonly authorized for CPT. In biotech and pharma, this includes research associate positions, analytical chemistry internships, regulatory affairs co-ops, clinical data management roles, bioinformatics positions, and process development internships. The role must be integral or directly related to your curriculum, and your DSO must authorize the CPT before you begin work.
How do I find biotech & pharma F-1 CPT sponsorship jobs in New Jersey?
Migrate Mate is built specifically for international students and filters jobs by visa type, making it straightforward to search for biotech and pharma roles in New Jersey that are open to F-1 CPT candidates. Rather than sifting through general job postings where sponsorship details are buried or absent, Migrate Mate surfaces positions where employers have indicated CPT eligibility, saving significant time during the job search. You can filter by location to focus on New Jersey's pharma corridors around Princeton, Rahway, and Parsippany.
Are there any New Jersey-specific or industry-specific considerations for F-1 CPT in biotech & pharma?
New Jersey's biotech and pharma sector frequently hires through structured internship and co-op cycles tied to university partnerships, particularly with Rutgers, Stevens Institute of Technology, and New Jersey Institute of Technology. Some larger employers require background checks or drug screenings before an internship start date, which can affect your CPT start timeline. Additionally, roles involving certain controlled substances, select agents, or export-controlled research may require additional compliance review that could complicate or delay onboarding for international students.