Full-Time

Senior Scientist I

Analytical Development

Confirmed live in the last 24 hours

Revolution Medicines

Revolution Medicines

201-500 employees

Specializes in precision oncology therapies

Biotechnology

Senior

San Carlos, CA, USA

Required Skills
Communications
Quality Assurance (QA)
Requirements
  • Ph.D. with a min of 8 years industry experience or MS degree with a min of 11 years of relevant industrial experience in analytical development.
  • Technical knowledge of analytical technologies including HPLC/UPLC, XRPD, LCMS, DSC, DVS and Dissolution.
  • Experience managing projects at CROs/CDMOs.
  • Work experience and knowledge of regulatory submission (IND, IMPD, and / or NDA).
  • Knowledge and understanding of current ICH guidelines, GMP guidelines, and related industry practices.
  • Strong problem-solving skills with sound technically driven decision-making ability.
  • Excellent scientific and business communication skills (verbal, written and technical), strong interpersonal/collaboration skills and planning skills.
  • Ability to think critically and creatively and be able to work independently to determine appropriate resources for resolution of problems.
  • Ability to multi-task and thrive in a fast-paced innovative environment.
Responsibilities
  • Provide support and oversight to analytical development activities, such as method development, method validation and testing, at contract partner sites to ensure outsourced activities are executed successfully and meet the objectives.
  • Provide analytical support for API process R&D and manufacturing, formulation development and drug product manufacturing, and participate in cross-functional project team meetings.
  • Critically review data packages associated with method validations, release testing, and other characterization testing for drug substances and drug products.
  • Collaborate with cross functional teams in the establishment of control strategy and setting specifications for drug substances and drug products.
  • Prepare, review, and/or approve study protocols, study reports, and CMC regulatory submission document.
  • Communicate technical findings to colleagues and collaborators within formal and informal settings, including cross-functional project team meetings.
  • 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.

### Welcome to Revolution Medicines, crafting the future of oncology with precision. Our focus is on advancing RAS(ON) inhibitors and RAS Companion inhibitors, marked by the remarkable journey of our lead product, RMC-4630, through its clinical phases. Supported by a team of passionate oncology experts, we are steadfast in our mission to develop treatments that precisely target oncogenic mutations, promising a brighter, healthier tomorrow for patients everywhere. ###

Company Stage

IPO

Total Funding

$1.3B

Headquarters

Redwood City, California

Founded

2014

Growth & Insights
Headcount

6 month growth

21%

1 year growth

48%

2 year growth

100%