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Scientist II, Process Chemistry

Revolution Medicines

Redwood City, CAHybridPosted 12 days ago$132,000 - $166,000/year
Full TimeEntry LevelManufacturing & CMCBiotechnology
Original posting ↗

Summary

We are seeking a gifted experimentalist to join our team as a laboratory-based process chemist to own development workstreams for a small-molecule drug substance. You will independently design and execute experiments, solve complex chemistry problems, and develop robust processes suitable for scale-up and technology transfer. This is a hands-on individual contributor role with responsibility for scientific recommendations and delivery of assigned development objectives.

Job description

The Opportunity

We are seeking a gifted experimentalist to join our team as a laboratory-based process chemist to own development workstreams for a small-molecule drug substance. You will independently design and execute experiments, solve complex chemistry problems, and develop robust processes suitable for scale-up and technology transfer. This is a hands-on individual contributor role with responsibility for scientific recommendations and delivery of assigned development objectives.

  • Own the development of reactions, process steps, or development workstreams, setting experimental approaches and coordinating work to meet agreed project objectives.
  • Design and execute experiments to evaluate alternative routes and optimize reactions, workup, isolation, and crystallization conditions.
  • Investigate complex reaction behavior and impurity formation using mechanistic reasoning, experimental design, comparison of analytical data, and understanding relevant scientific literature.
  • Develop robust processes by defining parameter sensitivity, reproducibility, impurity control, solubility limits, and other practical requirements for manufacturing.
  • Plan and execute laboratory studies and translate results into recommendations for process implementation at large-scale.
  • Prepare technology transfer procedures and work with external contract development and manufacturing organizations (CDMOs) to resolve implementation issues.
  • Author process development reports and technical content supporting regulatory documentation; maintain complete electronic laboratory records.
  • Provide scientific guidance to research associates, present recommendations to project teams, and identify and address laboratory and process safety risks.

Required Skills, Experience and Education

  • PhD in organic chemistry and at least 2 years of related experience, which may include postdoctoral research.
  • Demonstrated ability to independently design and execute process development studies and solve complex synthetic chemistry problems.
  • Strong hands-on skills in multistep synthesis, reaction optimization, isolation, and characterization using NMR, chromatography, and mass spectrometry.
  • Ability to connect experimental results with process robustness, scale-up considerations, and project objectives.
  • Experience taking responsibility for a defined scientific workstream and providing technical guidance to colleagues.
  • Clear scientific writing, effective collaboration, and proficiency with electronic laboratory notebooks, data analysis tools, and ChemDraw.

Preferred Skills

  • Industry experience in pharmaceutical process development, laboratory scale-up, crystallization, or technology transfer to CDMOs.
  • Experience with design of experiments, automated laboratory reactors, cGMP manufacturing, or drug substance regulatory documentation.

Requirements

  • PhD in organic chemistry
  • At least 2 years of related experience, which may include postdoctoral research
  • Demonstrated ability to independently design and execute process development studies and solve complex synthetic chemistry problems
  • Strong hands-on skills in multistep synthesis, reaction optimization, isolation, and characterization using NMR, chromatography, and mass spectrometry
  • Ability to connect experimental results with process robustness, scale-up considerations, and project objectives
  • Experience taking responsibility for a defined scientific workstream and providing technical guidance to colleagues
  • Clear scientific writing, effective collaboration, and proficiency with electronic laboratory notebooks, data analysis tools, and ChemDraw
  • Industry experience in pharmaceutical process development, laboratory scale-up, crystallization, or technology transfer to CDMOs
  • Experience with design of experiments, automated laboratory reactors, cGMP manufacturing, or drug substance regulatory documentation

Benefits

  • Equity Awards
  • Strong Benefits
  • Learning And Development Opportunities

Company overview

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies for RAS-addicted cancers. The company is pioneering a new class of therapeutics that target oncogenic RAS mutations, which are among the most common drivers of human cancers. Revolution Medicines employs a unique approach to drug discovery, leveraging deep insights into RAS biology to develop small molecule inhibitors that can address previously undruggable targets. Their pipeline includes multiple clinical-stage candidates designed to inhibit various RAS pathway mutations, with a particular focus on KRAS G12C and other RAS variants. The company's scientific platform combines structural biology, medicinal chemistry, and computational approaches to design highly selective inhibitors. Revolution Medicines aims to transform cancer treatment by developing therapies that can overcome resistance mechanisms and provide durable clinical benefits for patients with RAS-driven malignancies. Their research represents a significant advancement in the field of targeted cancer therapy, addressing one of the most challenging areas in oncology drug development.

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