Intern, Quality Assurance

Revolution Medicines is a clinical‑stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS‑addicted cancers. The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding Revolutionaries in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

• Support the Quality Assurance (QA) team in maintaining compliance with internal procedures, regulatory requirements, and quality standards.
• Assist with the review, organization, and maintenance of quality documentation, including SOPs, training records, and quality records.
• Participate in quality system activities such as deviations, CAPAs, change controls, and document control processes.
• Collaborate cross‑functionally with Manufacturing, R&D, and other teams to support quality initiatives and continuous improvement efforts.
• Gain hands‑on experience in a regulated biotech/pharmaceutical environment while developing a foundational understanding of GMP and quality systems.

• Currently pursuing a Bachelor’s or Master’s degree in Life Sciences, Engineering, Chemistry, Biology, Biotechnology, or a related field.
• Strong attention to detail with the ability to follow written procedures and maintain accurate records.
• Basic understanding of quality principles or regulated environments (academic coursework acceptable).
• Proficiency with Microsoft Office (Word, Excel, PowerPoint); ability to learn electronic quality management systems (eQMS).
• Strong written and verbal communication skills.
• Ability to work independently as well as collaboratively in a team environment.

• Prior internship, coursework, or laboratory experience in GMP, GxP, QA, QC, or manufacturing environments.
• Familiarity with FDA regulations, ICH guidelines, or ISO standards.
• Experience with document control systems, quality databases, or data analysis tools.
• Demonstrated interest in quality assurance, regulatory affairs, or compliance‑focused career paths.

Base pay salary range for this intern 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 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 is one part of the overall total rewards program at Rev Med, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.

Base Pay Salary Range

$67,000 — $81,000 USD

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.

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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 email address.

If you believe you’ve been contacted by someone impersonating a Revolution Medicines recruiter, please report it to so we can share these impersonations with our IT team for tracking and awareness.