What are the responsibilities and job description for the QC Intern position at Legend Biotech?
Company Information
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 and natural killer (NK) cell-based immunotherapy.
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) in 2017. 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.
Role Overview
The Quality Control Intern is a non-exempt level position responsible for working on assigned QC project identified as an improvement in relation to support the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment.
Key Responsibilities
Legend Biotech maintains a drug-free workplace.
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 and natural killer (NK) cell-based immunotherapy.
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) in 2017. 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.
Role Overview
The Quality Control Intern is a non-exempt level position responsible for working on assigned QC project identified as an improvement in relation to support the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment.
Key Responsibilities
- Work with QC Management and Equipment Specialist team to build up process to trend failure modes of QC instruments.
- Pull up reports from Maximo systems and summarize data into excel or other Microsoft tools applications.
- Create charts and graphs for monitoring failure modes for QC instruments.
- Any other activities as directed by supervisor.
- Pursuing a degree in science, Engineering or equivalent technical discipline is required.
- Microsoft office skills, able to create charts, presentations and data collection.
- Excellent written and oral communication skill are required.
- The candidate must be highly organized and capable of working in a team environment with a positive attitude under some supervision.Comfortable with speaking and interactions with others.
- This role is 100% onsite at the Raritan, NJ location.
Legend Biotech maintains a drug-free workplace.