Legend Biotech Jobs Hiring Now
Legend Biotech is hiring for 53 open roles on Migrate Mate as of August 31, 2026, concentrated in business operations and biotech & life sciences, with listed salaries up to about $444,000. Migrate Mate updates Legend Biotech's live openings daily. Legend Biotech is a biotechnology and pharmaceutical company focused on cell therapy research and development, with roles spanning scientific, clinical, quality assurance, and corporate functions.
Find Legend Biotech JobsOverview
Legend Biotech hiring data on Migrate Mate, as of August 31, 2026.
- Open jobs
- 53
- Top team
- Business Operations
- Seniority
- Manager level or above
- Work type
- 17% remote or hybrid
- Top location
- Somerset
- Salary range
- $48,000–$444,000
Listed salaries for Legend Biotech roles on Migrate Mate range from about $48,000 to $444,000 per year across 53 open roles, as of August 31, 2026.
Open Roles at Legend Biotech
Showing 25 of 53+ Legend Biotech jobs
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 IT Validation Analyst as part of the R&D Systems team based in Somerset, NJ.
Role Overview
The IT Validation Analyst is responsible for supporting and executing validation activities for GxP-regulated computerized systems. This role ensures systems are implemented, maintained, and operated in compliance with regulatory requirements and company procedures. The analyst works closely with IT, Quality Assurance, Business Process Owners, and vendors to ensure validated systems remain compliant throughout their lifecycle.
Key Responsibilities
- Execute and support Computer System Validation (CSV) and Computer Software Assurance (CSA) activities for GxP-regulated systems.
- Author and maintain validation documentation, including:
- Validation Plans
- User Requirements Specifications (URS)
- Risk Assessments
- Test Scripts (IQ/OQ/UAT)
- Traceability Matrices
- Validation Summary Reports
- Perform risk-based assessments to determine validation scope, testing requirements, and compliance impact.
- Coordinate and execute validation testing activities, document results, and ensure timely resolution of testing issues and deviations.
- Maintain and manage validation documentation and test execution activities using VLMS, EDMS, and QMS systems. Experience with ValGenesis and Veeva Quality Vault preferred.
- Support Change Controls, Deviations, CAPAs, and Periodic Reviews of GxP computerized systems to ensure systems remain in a validated state.
- Ensure compliance with applicable regulations, standards, and guidance.
- Assist during internal and regulatory audits by providing validation documentation and support.
- Provide guidance to system owners and project teams regarding validation requirements and best practices.
Requirements
- Bachelor's Degree in a Life Science, IT, Engineering or a related field
- 1-3 years of hands-on experience in Computer System Validation (CSV) within the biotech or pharmaceutical industries, experience with Computer Software Assurance (CSA) and AI a plus.
- Knowledge of Systems and Processes supporting: Quality, IT, Learning Management, Laboratory, Facilities, Equipment, and/or Manufacturing.
- Experience utilizing an automated Validation Lifecycle Management System (VLMS) for executing and managing periodic activities, validation deliverables, and testing activities.
- Demonstrated experience executing validation projects, creating and maintaining deliverables.
- Validation of AI and/or use of AI in validation activities in a GxP environment a plus.
- Knowledge and understanding of GxP regulations (FDA 21 CFR Part 11, EU Annex 11, GAMP 5, Data Integrity requirements) and their impact on CSV/CSA
- Experience in applying risk-based methodologies for CSV/CSA
- Experience in authoring validation deliverables (plans, specifications, test scripts, reports) and corresponding procedures
- Familiarity with use of electronic systems for Quality Management (QMS), Validation Lifecycle Management (VLMS), and Document Management (EDMS).
- Strong interpersonal, oral and written communication skills.
#Li-FB1
#Li-Hybrid
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.
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 IT Validation Analyst as part of the R&D Systems team based in Somerset, NJ.
Role Overview
The IT Validation Analyst is responsible for supporting and executing validation activities for GxP-regulated computerized systems. This role ensures systems are implemented, maintained, and operated in compliance with regulatory requirements and company procedures. The analyst works closely with IT, Quality Assurance, Business Process Owners, and vendors to ensure validated systems remain compliant throughout their lifecycle.
Key Responsibilities
- Execute and support Computer System Validation (CSV) and Computer Software Assurance (CSA) activities for GxP-regulated systems.
- Author and maintain validation documentation, including:
- Validation Plans
- User Requirements Specifications (URS)
- Risk Assessments
- Test Scripts (IQ/OQ/UAT)
- Traceability Matrices
- Validation Summary Reports
- Perform risk-based assessments to determine validation scope, testing requirements, and compliance impact.
- Coordinate and execute validation testing activities, document results, and ensure timely resolution of testing issues and deviations.
- Maintain and manage validation documentation and test execution activities using VLMS, EDMS, and QMS systems. Experience with ValGenesis and Veeva Quality Vault preferred.
- Support Change Controls, Deviations, CAPAs, and Periodic Reviews of GxP computerized systems to ensure systems remain in a validated state.
- Ensure compliance with applicable regulations, standards, and guidance.
- Assist during internal and regulatory audits by providing validation documentation and support.
- Provide guidance to system owners and project teams regarding validation requirements and best practices.
Requirements
- Bachelor's Degree in a Life Science, IT, Engineering or a related field
- 1-3 years of hands-on experience in Computer System Validation (CSV) within the biotech or pharmaceutical industries, experience with Computer Software Assurance (CSA) and AI a plus.
- Knowledge of Systems and Processes supporting: Quality, IT, Learning Management, Laboratory, Facilities, Equipment, and/or Manufacturing.
- Experience utilizing an automated Validation Lifecycle Management System (VLMS) for executing and managing periodic activities, validation deliverables, and testing activities.
- Demonstrated experience executing validation projects, creating and maintaining deliverables.
- Validation of AI and/or use of AI in validation activities in a GxP environment a plus.
- Knowledge and understanding of GxP regulations (FDA 21 CFR Part 11, EU Annex 11, GAMP 5, Data Integrity requirements) and their impact on CSV/CSA
- Experience in applying risk-based methodologies for CSV/CSA
- Experience in authoring validation deliverables (plans, specifications, test scripts, reports) and corresponding procedures
- Familiarity with use of electronic systems for Quality Management (QMS), Validation Lifecycle Management (VLMS), and Document Management (EDMS).
- Strong interpersonal, oral and written communication skills.
#Li-FB1
#Li-Hybrid
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.
Job Roles at Legend Biotech
Working at Legend Biotech
Legend Biotech's 53 open roles are manager level or above, and about 17% are remote or hybrid. The most active teams are business operations, biotech & life sciences, and laboratory research. Legend Biotech operates in the biotechnology and pharmaceutical sector, with work spanning cell biology research, analytical development, quality assurance, regulatory compliance, and corporate functions such as finance and organizational development. Most Legend Biotech roles are based in Somerset, with some in Bridgewater and Philadelphia.
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Browse jobs by roleLegend Biotech Jobs: Frequently Asked Questions
How many jobs is Legend Biotech hiring for right now?
Legend Biotech is hiring for 53 open roles on Migrate Mate as of August 31, 2026, updated daily, concentrated in business operations and biotech & life sciences. Open positions span scientific research, quality assurance, analytical development, finance, and compliance, reflecting activity across both laboratory and corporate functions.
What kinds of roles does Legend Biotech hire for?
The most active teams are business operations, biotech & life sciences, and laboratory research. Legend Biotech posts roles across cell biology research, analytical development, quality assurance, regulatory compliance, treasury, finance, and organizational development. Leadership development programs appear alongside individual contributor and specialist positions. Most postings are manager level or above, with a mix of scientist, manager, director, and analyst titles.
Are Legend Biotech jobs remote or in-person?
Mostly on-site. About 17% of Legend Biotech's open roles on Migrate Mate are remote or hybrid as of August 31, 2026, with the rest based in Somerset. Each Legend Biotech listing shows its work location so you can filter before applying.
How do I apply to a job at Legend Biotech?
Find a Legend Biotech role on Migrate Mate, then follow the listing through to Legend Biotech's own careers page to submit your application directly. Legend Biotech manages its own hiring process, including application review, interviews, and offers. Migrate Mate keeps Legend Biotech's listings current so you can check back as new roles open.
What do Legend Biotech jobs pay?
Listed salaries for Legend Biotech roles on Migrate Mate range from about $48,000 to $444,000 per year as of August 31, 2026, with most postings at manager level or above. Exact pay is set by Legend Biotech and shown on each listing.
Does Legend Biotech hire entry-level?
Most of Legend Biotech's open roles on Migrate Mate are manager level or above as of August 31, 2026. Entry-level openings are limited. Check individual Legend Biotech listings for stated experience requirements.
Where is Legend Biotech hiring?
Most Legend Biotech roles are based in Somerset, with some in Bridgewater and Philadelphia, and about 17% offer remote or hybrid work as of August 31, 2026. Migrate Mate shows the location on each listing.