Associate Director, Global Quality System & Compliance

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The companys R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The companys RAS(ON) inhibitors daraxonrasib (RMC-6236) a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291) a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805) a RAS(ON) G12D-selective inhibitor; and RMC-5127 a RAS(ON) G12V-selective inhibitor are currently in clinical development. As a new member of the Revolution Medicines team you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity:

• Provide strategic and operational leadership to scale and globalize the Quality Management System (QMS) establishing a harmonized flexible framework that supports international growth and regulatory compliance.

• Lead oversight and expansion of core quality systems across global sites including document control GxP training quality events supplier management audits and batch release.

• Partner with regional teams (including Japan Europe & other global regions) to integrate local regulatory requirements into the global QMS while maintaining global consistency.

• Establish and govern global quality procedures including policies SOPs and standardized processes to ensure compliance and operational efficiency.

• Ensure inspection readiness and lead support for global health authority inspections regulatory submissions and product launches.

• Oversee global quality metrics compliance monitoring and management review processes; drive proactive identification escalation and mitigation of quality risks.

• Provide governance for electronic quality and validated GxP systems (e.g. Veeva Vault Quality) ensuring they effectively support global operations.

• Collaborate cross-functionally to build and sustain a scalable quality infrastructure aligned with organizational growth and global expansion.

• Champion a culture of continuous improvement and quality excellence across the enterprise.

Required Skills Experience and Education:

• Bachelors degree in Life Sciences Pharmacy Chemistry or a related discipline (advanced degree preferred).

• Minimum of 10 years of experience in Quality within the pharmaceutical or biotechnology industry including leadership of global quality systems.

• Demonstrated experience establishing leading and maintaining a global Quality Management System (QMS) across multiple regions.

• Proven ability to influence and align senior stakeholders and executive leadership on quality strategy and risk-based decision making.

• Deep knowledge of global GxP regulations and experience ensuring compliance across international markets (e.g. FDA EMA PMDA).

• Proven track record supporting global regulatory filings approvals inspections and post-market quality obligations.

Preferred Skills:

• Experience building or transforming global QMS in a growing organization.

• Prior interaction with FDA EMA PMDA and other global health authorities.

• Experience supporting commercial product launches and lifecycle management.

  #LI-Hybrid #LI-JC1

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