Director, Supply Chain Business Systems
Revolution Medicines
Summary
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.
Job description
Key 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.
Required Skills, Experience and Education
- 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.
Preferred Skills
- Experience with Tracelink Serialization platform.
- Experience with ERP systems such as Netsuite and SAP.
- Familiarity with Veeva Development Cloud.
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.
- Experience with Tracelink Serialization platform.
- Experience with ERP systems such as Netsuite and SAP.
- Familiarity with Veeva Development Cloud.
Benefits
- Competitive cash compensation
- Equity awards
- Health benefits
- Learning and development opportunities
Company overview
Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies for RAS-addicted cancers. The company is pioneering a new class of therapeutics that target oncogenic RAS mutations, which are among the most common drivers of human cancers. Revolution Medicines employs a unique approach to drug discovery, leveraging deep insights into RAS biology to develop small molecule inhibitors that can address previously undruggable targets. Their pipeline includes multiple clinical-stage candidates designed to inhibit various RAS pathway mutations, with a particular focus on KRAS G12C and other RAS variants. The company's scientific platform combines structural biology, medicinal chemistry, and computational approaches to design highly selective inhibitors. Revolution Medicines aims to transform cancer treatment by developing therapies that can overcome resistance mechanisms and provide durable clinical benefits for patients with RAS-driven malignancies. Their research represents a significant advancement in the field of targeted cancer therapy, addressing one of the most challenging areas in oncology drug development.