Director, Supply Chain Business Systems

Revolution Medicines•Redwood City, CA

1d•Onsite

About The Position

Revolution Medicines is a global, commercial-stage oncology company dedicated to discovering, developing, and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide. Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency, and hold ourselves to a high standard of rigor—all in service of patients. The Opportunity: We are seeking a Director, Drug Supply Chain Business Systems to lead the systems and data capabilities that support the global movement of RevMed’s medicines from manufacturing through distribution. This role owns the roadmap for supply chain operations, packaging artwork, serialization, and product security, working closely with Supply Chain, Packaging, Quality, Regulatory, Security, and IT.

Requirements

Bachelor’s degree in information systems, supply chain, engineering, or a related field; advanced degree preferred.
10+ years of experience in business systems or supply chain technology, including significant experience in pharmaceuticals or another regulated life sciences environment.
Experience supporting a global supply chain across multiple regions, manufacturing sites, and distribution partners.
Experience with planning tools for clinical and commercial supply.
Demonstrated experience with pharmaceutical serialization systems, packaging line integration, aggregation, and partner data exchange.
Working knowledge of DSCSA and EU FMD requirements and experience supporting the systems used to meet them.
Experience with artwork management systems, packaging change processes, and product security capabilities.
Experience evaluating or deploying AI and automation in business processes, with sound judgment about data quality, oversight, and measurable value.
Working knowledge of 21 CFR Part 11, EU Annex 11, GAMP 5, and risk-based validation approaches.

Nice To Haves

Experience with Tracelink Serialization platform.
Experience with ERP systems such as Netsuite and SAP.
Familiarity with Veeva Development Cloud.

Responsibilities

Set the strategy and roadmap for global supply chain systems, including planning, inventory, order management, warehousing, distribution, artwork management, and serialization.
Lead serialization across packaging lines, enterprise systems, and external partners, including serial number management, aggregation, verification, and traceability data exchange.
Partner with Quality and Regulatory teams to support applicable U.S. Drug Supply Chain Security Act (DSCSA) and EU Falsified Medicines Directive (FMD) requirements.
Support artwork creation, review, approval, version control, and market-specific packaging changes.
Work with Quality and Security teams to strengthen counterfeit product prevention, product authentication, and investigations of suspect products.
Identify and implement AI opportunities that reduce manual work and improve decisions, such as inventory and demand analysis, exception triage, artwork review support, and detection of serialization data anomalies.
Measure results and maintain appropriate human review, data controls, and system oversight.
Lead system implementations and integrations, balancing global process consistency with local market requirements.
Maintain appropriate documentation, testing, change management, and data integrity.
Manage vendors, budgets, service performance, and teams.
Support continuity during product launches, recalls, and supply chain disruptions.