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:

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  Support the Quality Assurance (QA) team in maintaining compliance with internal procedures, regulatory requirements, and quality standards.

  
  


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  Assist with the review, organization, and maintenance of quality documentation, including SOPs, training records, and quality records.

  
  


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  Participate in quality system activities such as deviations, CAPAs, change controls, and document control processes.

  
  


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  Collaborate cross-functionally with Manufacturing, R&D, and other teams to support quality initiatives and continuous improvement efforts.

  
  


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  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:

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  Currently pursuing a Bachelor’s or Master’s degree in Life Sciences, Engineering, Chemistry, Biology, Biotechnology, or a related field.

  
  


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  Strong attention to detail with the ability to follow written procedures and maintain accurate records.

  
  


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  Basic understanding of quality principles or regulated environments (academic coursework acceptable).

  
  


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  Proficiency with Microsoft Office (Word, Excel, PowerPoint); ability to learn electronic quality management systems (eQMS).

  
  


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  Strong written and verbal communication skills.

  
  


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  Ability to work independently as well as collaboratively in a team environment.

  
  

Preferred Skills:

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  Prior internship, coursework, or laboratory experience in GMP, GxP, QA, QC, or manufacturing environments.

  
  


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  Familiarity with FDA regulations, ICH guidelines, or ISO standards.

  
  


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  Experience with document control systems, quality databases, or data analysis tools.

  
  


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  Demonstrated interest in quality assurance, regulatory affairs, or compliance-focused career paths. 

  
  

  #LI-Hybrid  #LI-AP1