Revolution Medicines

Scientist I, Drug Product

Revolution Medicines$119K — $149K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Degree in Pharmaceutical Science, Chemistry, Chemical Engineering, or related field
  • Ph.D. with 0-2 years of experience or bachelor's/master's with relevant experience
  • Academic or research background in drug product development
  • Knowledge of solid oral dosage forms and formulation principles
  • Familiarity with small molecule drug product concepts
  • Basic understanding of CMC principles and global regulatory guidelines
  • Strong communication and problem-solving skills

Responsibilities

  • Contribute to drug product development for new chemical entities from early to late-stage clinical development
  • Design and execute development activities for solid oral dosage forms
  • Support outsourced GMP drug product manufacturing at CDMOs
  • Conduct experiments, analyze data, and present findings
  • Work independently to troubleshoot technical challenges
  • Author CMC documentation for regulatory submissions
  • Collaborate with cross-functional teams to align development strategy
  • Travel up to 20% to support CDMO site operations

Benefits

  • Competitive cash compensation
  • Robust equity awards
  • Strong benefits program
  • Significant learning and development opportunities
Full Job Description
The Opportunity: The successful candidate will contribute to formulation and process development activities from early-stage through late-stage clinical/commercial development, working closely with cross-functional partners and CDMOs to ensure robust, scalable, and compliant drug product manufacturing processes. Key Responsibilities: • Contribute to drug product development activities for new chemical entities (NCEs) from early development through late-stage clinical development, with exposure to commercialization activities. • Design and execute drug product development and manufacturing activities for solid oral dosage forms, including: • Preformulation and formulation development • Manufacturing process development • Process scale-up, technology transfer, and process optimization • Process validation and commercial manufacturing support • Support outsourced development and GMP drug product manufacturing activities at CDMOs including manufacturing oversight and troubleshooting. • Design and execute experiments, analyze and interpret data and present results and conclusions to project teams. • Work independently with limited supervision to conduct appropriate research and troubleshoot technical challenges, escalating complex issues as needed. • Author and contribute to CMC documentation for regulatory submissions (e.g., INDs, NDAs, MAAs) and internal technical reports. • Collaborate cross-functionally within CMC team (Clinical Supply, Analytical Development/QC, Quality Assurance, Drug Substance, Regulatory Affairs, and Project Management) and at enterprise level research/clinical/commercial teams to support aligned development strategy and execution. • Travel up to 20% to CRO/CDMO sites to support and oversee development and manufacturing operations. Required Skills, Experience and Education: • A degree in Pharmaceutical Science, Chemistry, Chemical Engineering, or closely related field is desirable. • D. with 0-2 years of experience or a bachelor's/master's degree with appropriate experience in the pharmaceutical/biotech industry settings. • Academic or research experience relevant to drug product development, formulation, pharmaceutical sciences, or small molecule development is preferred. • Knowledge of solid oral dosage forms, formulation principles, and pharmaceutical manufacturing processes gained through graduate research, coursework, internships, or related training is desirable. • Familiarity with formulation and process development concepts for small molecule drug products is preferred. • Basic understanding of pharmaceutical development, CMC principles, and global regulatory guidelines, including ICH guidelines, is desirable. • Exposure to working in multidisciplinary or collaborative research environments, including interactions with internal or external scientific partners, is a plus. • Strong scientific, technical writing, communication, and problem-solving skills. • Demonstrated ability to analyze experimental data, draw scientifically sound conclusions, and communicate results effectively. • Ability to learn quickly, manage multiple priorities, and work effectively in a fast-paced, innovation-driven, collaborative environment. Preferred Skills: • Ph.D. degree in Pharmaceutical Science, Chemistry, Chemical Engineering, or closely related field is desirable. 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. Base Pay Salary Range $119,000-$149,000 USD 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 [email protected] so we can share these impersonations with our IT team for tracking and awareness.

About Revolution Medicines

Revolution Medicines is a clinical-stage precision oncology company focused on developing targeted therapies to inhibit elusive frontier targets within notorious growth and survival pathways, with particular emphasis on RAS and mTOR signaling pathways. The company's proprietary platform enables the discovery and development of small molecules that bind covalently to proteins. Revolution Medicines was founded in 2014 and is headquartered in South San Francisco, California.
Learn more about Revolution Medicines
Size
201 employees
Market Cap
$2.1 billion
Industry
Net Income
-$108.1 million
Revenue
$42.9 million
NASDAQ

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