Associate Director, Strategic Sourcing and Supplier Management

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s 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: Serve as Revolution Medicines’ business operations lead interface between internal PDM functions and Contract Research Development Manufacturing Organization (CRDMOs) for drug product manufacturing and packaging. Manage CRDMO requests for proposals, proposal review, negotiation, RevMed governance approval, legal review, purchase order issuance and invoice approval. Lead preparation and execution of CRDMOs business reviews with SSSM leadership, PDM senior management, and business counterparts. Ensure projects/programs meet desired results, compliance, speed, quality, and cost. Support contract negotiations in close collaboration with SSSM leadership and cross-functional teams (e.g., Subject Matter Experts (SMEs), Finance, and Legal) to ensure best terms and conditions. Support development and implementation of outsourcing strategies for PDM. Support the selection process for CRDMOs in collaboration with SSSM leadership and technical SMEs. Support cross-functional CRDMO management activities, covering all aspects such as business needs identification, contracting, vendor qualification and set-up, compliant delivery of services, and discontinuation. Work with SSSM leadership, PDM senior management, and cross-functional teams to assess and manage supplier performance through use of personal influence, internal business review meetings, and/or joint governance meetings. Identify and deliver on cost savings opportunities. Required Skills, Experience and Education: B.Sc. in Supply Chain, Engineering, Business, Life Sciences, or related field plus 8+ years of experience in pharmaceutical strategic sourcing and/or commercial supply chain. Experience working with domestic and international drug product CRDMOs. Experience managing tactical/operational projects. Working knowledge of and experience in drug product manufacturing, packaging and distribution, regulatory, QA, and cGMP requirements for pharmaceutical products. Working knowledge of drug development. Working knowledge of pharma end-to-end supply chain. Strong negotiation skills. Solid project management, facilitation, and problem-solving skills. Solid organizational and time management skills. Effective, open, and transparent communication skills (verbal and written). Capable of working on multiple projects/tasks and able to meet timelines. Self-starter with a high-level of comfort with ambiguity and complexity and the ability to multi-task while consistently delivering quality results. Team-oriented, progressive thinker who enjoys participating in an innovative and creative work environment. Preferred Skills: Experience developing, negotiating, and executing clinical or commercial supply and/or quality agreements. Experience in drug product manufacturing and packaging operations. Experience with Project Management software (i.e. Smartsheet) and ERP systems (i.e. NetSuite). Experience leading Technical Transfers. Experience working with Ex-US suppliers. #LI-CT1 #LI-Hybrid The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual workin…