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.

The Opportunity:

• 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.

Required Skills, Experience and Education:

• 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.

Preferred Skills:

• 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. 

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