[Hiring] Director, GxP Quality Governance and Partnerships @Revolution Medicines

Role Description

The Director, GxP Quality Governance & Partnerships will provide Quality leadership in establishing and managing Quality Agreements and related arrangements supporting Revolution Medicines’ expanding global development, manufacturing, and commercial operations.

• Lead the development, review, negotiation, and execution of Quality Agreements and related Quality arrangements supporting clinical development and global commercial operations.
• Manage agreements involving CMOs, CDMOs, contract laboratories, packaging and distribution partners, clinical collaborations, other GxP service providers, and intra-company arrangements.
• Establish clear Quality responsibilities, decision-making authority, oversight expectations, and communication requirements across internal and external partnerships.
• Collaborate with Legal, Strategic Sourcing, Regulatory Affairs, Supply Chain, Technical Operations, Clinical Operations, and other stakeholders to align Quality Agreements with business contracts, operational needs, and applicable regulatory requirements.
• Lead the resolution of complex agreement-related issues and negotiations, making timely, risk-based decisions and escalating significant risks or unresolved matters to the appropriate leadership or cross-functional teams.
• Develop and implement a risk-based Quality Agreement lifecycle management framework, including templates, workflows, tracking, periodic reviews, amendments, and renewals.
• Establish effective Quality governance practices for external partnerships, including accountability, communication channels, review mechanisms, and oversight of agreed Quality commitments.
• Partner with operational Quality teams to ensure agreements remain aligned with actual activities, regulatory expectations, and evolving partnership arrangements.
• Support new product launches, geographic expansion, and changes to development and commercial supply networks by establishing appropriate Quality arrangements.
• Identify and implement opportunities to improve processes, cross-functional collaboration, and efficiency in managing external Quality partnerships.
• Contribute to broader external partner Quality oversight, supplier management, and strategic compliance initiatives as organizational needs evolve.

Qualifications

• Bachelor’s degree in life sciences, technical, or related field with 12+ years of experience in the biotechnology, pharmaceutical, or medical device industry.

Requirements

• Experience supporting Quality Agreements or external Quality partnerships across multiple GxP disciplines.
• Experience working with global partners and regulatory requirements across the US, Europe, Japan, China, Canada, and other markets.
• Experience developing or improving agreement management processes, Quality governance frameworks, or external partner oversight programs.
• Experience supporting commercial product launches, geographic expansion, or complex business partnerships.
• Experience with supplier qualification, audits, or ongoing Quality oversight of external partners.
• Experience building scalable processes and programs in a rapidly growing organization.

Benefits

• Competitive cash compensation.
• Robust equity awards.
• Strong benefits.
• Significant learning and development opportunities.

Company Description

Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. The company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS.