Job Description

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 scientists in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity:

Playing an important role as engineering support within the Drug Product team and working closely with Scientists and Process Engineers within the group. A successful candidate will be responsible for supporting clinical-stage and late-stage process developments as well as supporting preparation for Process Performance Qualification of Revolution Medicines’ compounds.

• Work closely with Scientists and Process Engineers within Drug Product group to support the transition of drug product manufacturing from clinical stage development through late-stage development and Process Performance Qualification (PPQ).

• Support formulation and process development and optimization studies conducted according to the principles of Quality by Design (QbD), using tools such as OFAT (one factor at a time) experiments and DOE (Design of Experiments).

• Review protocols, manufacturing batch records, and development, campaign, and technical reports for clinical-stage and late-stage manufacturing.

• Analyze data and perform statistical analysis to support process development and optimization, process capability, and process range justification.

• Build and maintain databases to manage and track experimental data and results for multiple programs.

• Conduct literature reviews and stay updated on the latest advancements in drug product development and manufacturing.

Required Skills, Experience and Education:

• Working towards a BS or MS or Ph. D in Chemical Engineering, Pharmaceutical Sciences, or related discipline.

• Strong problem-solving skills with sound technically driven decision-making ability.

• Effective written and verbal communication skills and interpersonal skills.

• Ability to review and interpret technical documents and protocols.

• Strong organizational skills and attention to detail.

• Ability to work collaboratively in a team environment.

• Able to complete a 10-12 consecutive week internship between June and August 2025.

Preferred Skills:

• Proficiency in statistical analysis software (JMP).

• Knowledge of Quality by Design (QbD) principles and tools such as OFAT and DOE.

• Familiarity with regulatory requirements and guidelines in the pharmaceutical industry.

The base salary range for this temporary position is $32.75 to $35.00 for candidates based at our headquarters in Redwood City, CA. The range displayed on each job posting is intended to be the minimum and maximum salary for the position in Redwood City and will be adjusted for the local market a candidate is based. Our salary ranges are determined by role, level, and location. Individual pay is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.

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 the 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.