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QA Document Control Specialist I
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- 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.
- Legend Biotech is seeking QA Document Control Specialist as part of the Quality team based in Raritan, NJ.
- The Quality Assurance Document Control Specialist role is an exempt position responsible for supporting the document management process within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment.
- This role will ensure compliance within the document management system, document storage & retention, and document issuance & reconciliation.
- Responsible for storage and archival of GMP documents and batch related records.
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