Senior GMP QA Lead for Small Molecule DS/DPI

Revolution Medicines; San Francisco (CA); On-site; USD 180,000 - 240,000; Full time

Job summary

Revolution Medicines, Inc. in San Francisco, CA, seeks an Associate Director for GMP Quality Assurance to oversee DS/DPI batches, ensure GMP compliance, and support CMC submissions. You will partner with Technical Operations and CDMOs to maintain quality and inspection readiness for clinical and commercial programs.

Ideal candidates bring 10+ years in GMP quality, strong risk assessment and leadership, and experience with DS/DPI manufacturing, validation, and regulatory filings.

Qualifications

• 10+ years in GMP quality.
• Experience with DS/DPI manufacturing.
• Experience with regulatory filings and submissions.

Responsibilities

• Oversee DS/DPI batches to ensure GMP compliance.
• Partner with Technical Operations and CDMOs to maintain quality and inspection readiness.
• Support CMC submissions and regulatory filings for clinical and commercial programs.

Skills

GMP quality

Risk assessment

Leadership

DS/DPI manufacturing

Regulatory filings

Job description

Revolution Medicines, a late-stage clinical oncology company, seeks an Associate Director for GMP Quality Assurance to oversee DS/DPI batches, ensure GMP compliance, and support CMC submissions. You will partner with Technical Operations and CDMOs to maintain quality and inspection readiness for clinical and commercial programs.

Ideal candidates bring 10+ years in GMP quality, strong risk assessment and leadership, and experience with DS/DPI manufacturing, validation, and regulatory filings.