Associate Director, Drug Substance
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Job Location:
Redwood City, CA - USA
Monthly Salary:
Not Disclosed
Posted on:
08-11-2025
Vacancies:
1 Vacancy
Job Summary
Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The companys 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 Revolutionariesin a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.
The Opportunity:
Playing a critical role as a technical lead within the Drug Substance function the position will be responsible for process research and development and scale-up of manufacturing in support of Revolution Medicines pipeline compound development clinical programs and commercial readiness.
Responsibilities:
Responsible for developing chemical processes for the manufacture of drug substance intermediates and/or starting materials.
Manage sourcing and manufacture of raw materials intermediates and regulatory starting materials and be accountable to project team to meet aggressive timelines .
Lead and/or enable technology transfer process familiarization and manufacturing at CDMOs.
Participate in identification selection and management of CROs and CDMOs including management of redundant supply and geographic diversity.
Conduct process development and optimization studies according to the principles of quality by design (QbD) to enable regulatory starting materials designation establish control strategy and process characterization studies using tools such as design of experiment (DOE) studies
Propose and/or develop alternative chemistry for drug substance and intermediates including route evaluation and process optimization.
Write review and approve protocols manufacturing batch records and development and campaign reports.
Author review the relevant CMC sections of regulatory filings and patent applications.
Partner with analytical development pharmaceutical development and supply chain functions to design overall strategy for programs.
Communicate effectively within cross functional project teams.
Travel to CRO/CDMO for the oversight of development activities and manufacturing (up to approximately 15%).
Required Skills Experience and Education:
PhD with 8 or more years or minimum Masters degree with 10 years of relevant industrial experience in chemical / drug substance process research and development.
8 or more years of relevant industrial experience in chemical / drug substance process research and development.
Strong people management skills.
Hands-on proficiency in synthetic organic chemistry.
Knowledge of current ICH guidelines GMP and relevant industry practices.
Working experience and knowledge of regulatory submissions (IND IMPD NDA and MAA).
Previous experience managing projects at CROs/CDMOs.
Strong problem solving skills with sound technically driven decision-making ability.
Effective written and verbal communication skills and interpersonal skills.
An innovative team-player with high energy for our dynamic company environment.
Preferred Skills:
PhD (minimum Masters degree) in organic chemistry chemical engineering or related discipline. #LI-Hybrid #LI-CT1
The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role level and location. Individual base pay salary is determined by multiple factors including job-related skills experience market dynamics and relevant education or training.
Please note that base pay salary range is one part of the overall total rewards program at RevMed which includes competitive cash compensation robust equity awards strong benefits and significant learning and development opportunities.
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 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 ourCCPA additional information please contact.
Required Experience:
Director
Key Skills
- Program assessment
- FDA Regulations
- Manufacturing & Controls
- Program Evaluation
- budget forecast
- Research Experience
- Operations Management
- Research & Development
- Strategic Planning
- Contract Management
- Leadership Experience
- negotiation
