Intern, Quality Assurance
About The Position
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: 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.
Requirements
- 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.
Nice To Haves
- 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.
Responsibilities
- 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.
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What This Job Offers
Career Level
Intern
Number of Employees
251-500 employees
