Quality Systems Specialist - GxP Documentation & QA
ORIC Pharmaceuticals Inc.
ORIC Pharmaceuticals Inc. is seeking a document control/QA support role to manage regulated GxP documents, ensuring timely review and release. You will collaborate with document owners to resolve discrepancies and support cross-functional QA updates. Responsibilities include maintaining electronic quality systems, SOPs, and training coordination, while supporting audits and inspections and adhering to ORIC’s policies and regulatory requirements. #J-18808-Ljbffr ORIC Pharmaceuticals Inc.
Vacancy posted 4 days ago
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