Scientist II, Drug Product

Role: Scientist II supporting drug product development within Pharmaceutical Development & Manufacturing for Revolution Medicines' small molecule oncology pipeline. Responsibilities: design and execute formulation and process development activities for solid oral dosage forms across clinical stages; oversee outsourced manufacturing at CDMOs; contribute to regulatory CMC documentation; collaborate cross-functionally with teams including Analytical, Quality, Regulatory, and Clinical; support scale-up, tech transfer, and troubleshooting; travel up to 20% to external sites. Requirements: Ph.D. with 3+ years or Bachelor's/Master's with relevant industry experience; expertise in small molecule formulation and process development; experience managing external manufacturing partners; knowledge of global regulatory frameworks (FDA, EMA, ICH); strong technical writing and problem-solving skills. Preferred: advanced degree in Pharmaceutical Science, Chemistry, or Chemical Engineering. High-Value: small molecule solid oral drugs, early to late-stage clinical development, CMC regulatory contributions, GMP compliance, cross-functional collaboration, international regulatory knowledge, and external partner oversight. Work setup: onsite in Redwood City, CA, with travel to CRO/CDMO sites.