Quality Systems Lead ISO 13485 FDA for Cell Therapies
XDemics Corporation
XDemics Corporation in San Francisco, CA, is seeking a highly organized Quality Specialist to establish and maintain an ISO 13485 and FDA QSR–compliant quality system supporting the development and production of our cell culture products as Class I medical devices. You will lead CAPAs, audits, documentation, and compliance activities across R&D, Manufacturing, and Regulatory Affairs, ensuring quality is built into all processes and driving continuous improvement in a fast-growing startup. #J-18808-Ljbffr XDemics Corporation
Vacancy posted 15 hours ago
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