Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide.
Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients.
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Lead day-to-day operations to provide analytical support for API process R&D and manufacturing, formulation development and drug product manufacturing, and participate in cross-functional project team meetings.
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Contribute to analytical development strategy for multiple projects.
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Demonstrate technical expertise on analytical technologies and act as a subject matter expert for Analytical Development function.
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Select appropriate analytical techniques and coach and/or manage the contract lab counter parts to perform analytical method development/validation/transfer to support development and manufacturing of API and drug product.
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Critically review data from contract partners (CDMOs and/or CTLs).
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Manage stability testing programs assigned.
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Prepare, review, and/or approve study protocols, study reports, and CMC regulatory submission document.
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Collaborate with cross functional teams including but not limited to Medicinal Chemistry, DMPK, Toxicology, QA, Pharmaceutical Development, Process R&D, Project Management and Regulatory to timely achieve project goals.
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Master’s degree with 10+ years or PhD with 8+ years of relevant industrial experience in analytical development.
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Extensive experience leading analytical activities independently in small molecule drug development.
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Experience managing projects at CROs/CDMOs.
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Work experience and knowledge of regulatory submission (IND, IMPD, and / or NDA).
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Effective written and verbal communication skills and interpersonal skills.
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Extensive knowledge and understanding of current ICH guidelines, GMP guidelines, and related industry practices.
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Strong problem-solving skills with sound technically driven decision-making ability.
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Excellent scientific and business communication skills (verbal, written and technical), strong interpersonal/collaboration skills and planning skills.
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Ability to think critically and creatively and be able to work independently to determine appropriate resources for resolution of problems.
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Ability to multi-task and thrive in a fast-paced innovative environment.
We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.
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 @revmed.com email address.
If you believe you’ve been contacted by someone impersonating a Revolution Medicines recruiter, please report it to careers@revmed.com so we can share these impersonations with our IT team for tracking and awareness.
