Senior Associate Director, QC & Analytical Development

Revolution Medicines; Redwood City, Northern (CA, KY); Hybrid; USD 186,000 - 233,000; Full time

Job summary

Revolution Medicines is seeking an Associate Director of Analytical Development & QC in Redwood City, CA. This role leads QC testing for late-stage and commercial programs, manages method transfers, and coordinates with CMC RA, DS, DP, Supply Chain and QA to maintain regulatory compliance and testing quality.

Responsibilities include vendor oversight at CDMOs/CTLs, handling deviations and CAPAs, and driving continuous improvement to support launches and product quality.

Qualifications

• Bachelor’s degree in a scientific discipline with 15+ years of experience in pharmaceutical QC operations across development and commercial stages.
• Alternative: Master’s degree with 12+ years or PhD with 10+ years accepted.

Responsibilities

• Lead and oversee QC activities of late-phase and commercial programs, including launch readiness and in-process control testing.
• Oversee outsourced QC activities at CDMOs and contract testing labs (CTLs).
• Manage quality events such as deviations, CAPAs, OOS/OOT, and change controls.
• Author and review commercial QC related documents, including methods, protocols, reports and memos.
• Collaborate with CMC RA, DS, DP, Supply Chain and QA to achieve project goals.

Job description

Revolution Medicines is seeking an Associate Director of Analytical Development & QC in Redwood City, CA. This role leads QC testing for late-stage and commercial programs, manages method transfers, and coordinates with CMC RA, DS, DP, Supply Chain and QA to maintain regulatory compliance and testing quality.

Responsibilities include vendor oversight at CDMOs/CTLs, handling deviations and CAPAs, and driving continuous improvement to support launches and product quality.