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 the Computer System Validation (CSV) QA subject matter expert and provide guidance on the interpretation and application of global GxP regulations and guidance related to computerized systems, electronic records, electronic signatures, and data integrity, including FDA 21 CFR Part 11, EU Annex 11, and GAMP principles.
Provide Quality Assurance oversight of CSV activities for internal and external GxP computerized systems, ensuring validation activities are conducted in compliance with regulatory requirements and company Software Development Life Cycle (SDLC) standards.
Implement and promote best practices for data governance and data integrity, ensuring computerized systems meet GxP compliance requirements throughout their lifecycle.
Lead and provide oversight for Data Integrity and Computer System Validation programs and activities.
Review and approve CSV documentation, including validation plans, requirements, risk assessments, test protocols, validation reports, and system retirement documentation.
Review and approve GxP change controls, deviations, CAPAs, and other quality records to ensure compliance with quality and regulatory requirements.
Lead supplier audits, assessments, qualification, and requalification activities for electronic system vendors and service providers.
Support the development, implementation, and continuous improvement of computerized system policies, procedures, validation methodologies, and quality processes.
Collaborate cross-functionally to identify compliance risks, process gaps, and opportunities for improvement, and drive implementation of effective solutions.
Provide guidance, education, and training to cross-functional teams on risk-based validation approaches and GxP system deployment.
Support inspection readiness initiatives and represent Quality Assurance during partner audits, customer audits, and regulatory inspections.
Monitor evolving regulatory expectations and industry trends related to computerized systems validation, data integrity, and digital quality systems.

Required Skills, Experience and Education:

Bachelor’s degree in computer science, Information Systems, Engineering, Life Sciences, or a related discipline, or equivalent combination of education and experience.
Minimum 8 years of Quality Assurance experience in the pharmaceutical, biotechnology, or life sciences industry supporting GxP computerized systems.
Extensive experience in Computerized Systems Validation (CSV) and/or Computer Software Assurance (CSA) with strong knowledge of GAMP 5, SDLC, and risk-based validation methodologies.
Expert knowledge of FDA 21 CFR Part 11, EU Annex 11, Data Integrity, and ALCOA+ principles, including electronic records and electronic signatures compliance requirements.
Broad experience with GxP computerized systems and the ability to author, review, and approve validation deliverables, risk assessments, testing documentation, and compliance-related records throughout the system lifecycle.

Preferred Skills:

Experience supporting regulatory inspections, internal audits, and supplier/vendor audits.
Familiarity with cloud-based/SaaS platforms, vendor qualification, and third-party risk management.
Excellent analytical, problem-solving, and cross-functional collaboration skills.

#LI-Hybrid #LI-JC1

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 working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.

Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.

Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.

Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact privacy@revmed.com.

Base Pay Salary Range

$164,000—$205,000 USD

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Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address.

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Senior Manager, GxP Electronic System Validation QA