What are the responsibilities and job description for the Quality Assurance Validation Intern position at legendcareers?
Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide.
Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma.
Legend Biotech is seeking a Quality Assurance Validation Intern as part of the Quality team based in Raritan, NJ.
Role Overview
The QA Validation Intern will support validation activities by organizing and tracking documentation, assisting with QA release processes, and maintaining compliance records. This role provides exposure to GMP documentation practices and quality assurance workflows.
Key Responsibilities
- Organize and track document spreadsheets for validation activities.
- Print QA release labels and file release copies to Cartna.
- Pick up and deliver documents between departments and buildings.
- Compose a list of site SOPs sorted by topic.
- Support QA team with administrative and compliance tasks.
Requirements
- Enrolled in an undergraduate program (Desired Academic Grade Level: Junior/ Senior)
- Strong working knowledge of Excel.
- Ability to work collaboratively in a team environment.
- Strong organizational and presentation skills.
Skills You'll Gain
- Hands-on experience with QA validation processes.
- Exposure to GMP documentation and compliance standards.
- Development of organizational and communication skills.
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Please note: These benefits are offered exclusively to permanent full-time employees. Contract employees are not eligible for benefits through Legend Biotech.
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.