Director, Stability Programs & Regulatory Readiness

Revolution Medicines; San Francisco (CA); On-site; USD 211,000 - 264,000; Full time

Job summary

Revolution Medicines is seeking a Stability Program Lead in San Francisco, CA. This full-time position involves overseeing the management of outsourced stability studies and ensuring compliance with ICH and GMP guidelines. Candidates should hold a PhD in Chemistry or Pharmaceutical Sciences with extensive industry experience. A salary range of $211,000 - $264,000 is offered for onsite positions. This role requires strong leadership, project management, and communication skills, with a focus on supporting regulatory filings and improving stability processes.

Qualifications

• 12+ years of industry experience in required fields.
• Strong knowledge of GMP regulations and ICH guidelines.
• Extensive experience managing contract organizations.

Responsibilities

• Oversee and manage outsourced stability studies.
• Develop and implement strategic direction of stability programs.
• Compile study results and prepare reports for regulatory filings.

Skills

Stability management experience

Leadership skills

Project management skills

Communication skills

Problem-solving skills

Education

PhD in Chemistry or related discipline

MS with 15+ years of experience

BS with 18+ years of experience

Job description

Revolution Medicines is seeking a Stability Program Lead in San Francisco, CA. This full-time position involves overseeing the management of outsourced stability studies and ensuring compliance with ICH and GMP guidelines. Candidates should hold a PhD in Chemistry or Pharmaceutical Sciences with extensive industry experience. A salary range of $211,000 - $264,000 is offered for onsite positions. This role requires strong leadership, project management, and communication skills, with a focus on supporting regulatory filings and improving stability processes.