GRAIL is a healthcare company whose mission is to detect cancer early, when it can be cured. GRAIL is focused on alleviating the global burden of cancer by developing pioneering technology to detect & identify multiple deadly cancer types early. The company is using the power of next-generation sequencing, population-scale clinical studies, & state-of-the-art computer science & data science to enhance the scientific understanding of cancer biology, & to develop its multi-cancer early detection blood test. GRAIL is headquartered in Menlo Park, CA with locations in Washington, D.C., North Carolina, & the United Kingdom. GRAIL is a wholly-owned subsidiary of Illumina (NASDAQ:ILMN). For more information, please visit www.grail.com
The Staff Quality Engineer will act as a key liaison for quality with reagent manufacturing operations & reagent QC. This individual will be responsible for process execution to Current Good Manufacturing Practices (cGMPs), GCP, ISO 13485, FDA 21 CFR part 820, & an understanding of CLIA, CAP, & New York State Licensures for LDTs. Support/complete mfg batch record review & reagent release, NCR Lifecycle, Material Management, Specification development, validation support, CAPA's, & Quality Systems & Audit support. This position is required to be onsite at RTP (North Carolina).