Validation Lead
Revolution Medicines
Revolution Medicines seeks an experienced Associate Director, IS Quality and Compliance to lead CSV/CSA for GxP systems in the Information Sciences organization at our Redwood City headquarters. You will oversee validation lifecycle activities, data integrity, electronic records, and regulatory inspection readiness, while mentoring teams and partnering with Quality and business stakeholders to maintain compliance. #J-18808-Ljbffr
Vacancy posted 4 days ago
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