El Segundo, CA21 days ago
li>Generate, support and execute validation protocols (IQ/OQ/PQ/CV/PV) of all site equipment including laboratory equipment, production equipment, utilities (as applicable) and other related systems in an FDA regulated environment, Author and review SOPs, protocols, reports, and validation master plans for GMP equipment, instruments, and computerized systems, Generate and keep current inventory of GMP systems and requalification/periodic review schedules, Perform and lead risk assessments for GMP systems as required, Plan validation efforts according to risk, Collaborate with clients, CMOs, and vendors to meet project and company objectives, Assist with vendor communications, Troubleshoots and resolve discrepancy reported during validation/qualification. ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells.