Associate Director, Quality Systems

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The companys R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team you will join other outstanding Revolutionariesin a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity:

• Provide leadership and operational oversight for enterprise quality systems with primary accountability for GxP Document Control GxP Training and Veeva Quality Suite platform governance.

• Develop and execute the global Quality Systems strategy in alignment with company goals and regulatory expectations.

• Build lead and mentor a high-performing team responsible for Document Control GxP Training and Veeva Quality Suite operations.

• Provide strategic leadership by mentoring and coaching direct reports translating organizational and Quality goals into clear departmental objectives and fostering a culture of accountability continuous improvement and operational excellence.

• Serve as Global Process Owner for Document Control ensuring GxP documentation is compliant controlled and inspection/Audit ready in accordance with region specific regulatory requirements.

• Responsible for document retention archival and electronic data archival. Oversees the development review approval issuance and archival of controlled documents in compliance with applicable regulatory requirements and internal quality standards.

• Provide strategic oversight of the global GxP Training Program including governance curriculum design and role-based training matrices.

• Ensure global training compliance deploy scalable training solutions and implement system integrations to support organizational growth.

• Define and monitor training metrics to ensure accountability and continuous improvement.

• Act as Business Process Owner for Veeva Quality Suite platforms and oversee configuration enhancements integrations and release management.

• Ensure data integrity workflow efficiency and strong user adoption across GxP functions by implementing robust data governance and data management aligned with ALCOA principles.

• Oversee Veeva QualitySuite system validation upgrades and compliance with 21 CFR Part 11 and Annex 11.

• Support audit and inspection support activities including document retrieval training records and system demonstrations.

• Establish and manage global KPIs/KQIs for Document Control Training and Veeva platform performance.

• Lead cross-functional quality improvement projects to simplify processes reduce cycle times and increase automation.

• Proactively identify and implement opportunities to strengthen compliance efficiency and user experience.

Required Skills Experience and Education:

• Bachelors degree in Life Sciences Engineering or related field required; advanced degree preferred.

• Minimum 12 years of progressive GxP Quality systems experience in the biopharmaceutical or related industry.

• Minimum 5 years of leadership experience managing global quality systems teams.

• Deep expertise in Veeva Quality Suite (QualityDocs Training and related QMS modules).

• Strong knowledge of global GxP regulations and expectations (FDA EMA ICH).

• Demonstrated success in building and leading high-performing teams.

• Experience supporting global regulatory inspections and audits.

Preferred Skills:

• Leadership experience supporting late-stage development and commercial launch readiness.

• Experience in both virtual sponsor and scaling global organization models. #LI-Hybrid #LI-JC1