Executive Director, Quality Control

Revolution Medicines•Redwood City, CA

23h•$256,000 - $320,000•Hybrid

About The Position

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding Revolutionaries in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity: Playing a critical role as the QC group leader and QC subject matter expert (SME) within Analytical Development (AD) & Quality Control (QC), Pharmaceutical Development and Manufacturing (PDM) department, the position will be responsible for managing clinical and commercial Quality Control (QC) activities from early to late phase development, process validation, commercial launch in support of RevMed’s pipeline development. The candidate will also be responsible for post-approval QC related activities including commercial supplies, lifecycle management, regulatory submissions (e.g., CBE, PAS). Partner with senior leadership on QC-related strategic development and implement QC policies and practices. Lead the QC team, providing technical and strategic leadership for day-to-day QC activities supporting clinical and commercial programs. Responsibilities include preparation for commercial product launches, management of quality events (e.g., lab investigations for OOS/OOT, deviations, CAPAs). Direct key QC programs including stability, reference standard, raw material, QC quality systems, procedures, and documentation (e.g., SOPs), PAI readiness, and regulatory inspections. Manage the selection, oversight, and performance management of contract organizations (COs), ensuring the effective outsourcing and execution of clinical and commercial QC activities. Author, review, and approve QC-related documentation, including analytical methods, protocols, reports, and regulatory submissions. Partner with cross-functional teams such as CMC Regulatory Affairs, Drug Substance, Drug Product, Supply Chain, and Quality Assurance to ensure timely achievement of project milestones and objectives.

Requirements

BS, MS, or PhD in Chemistry, Pharmaceutical Science, or a related field.
20+ years of relevant industry experience in small molecule Analytical Development and Quality Control, with at least 8 years in a senior leadership role.
Deep knowledge of global and regional regulatory guidelines (FDA, EMA, ICH, USP etc.), particularly in areas such as method development/validation, process validation, product launches, commercial manufacturing, and post-approval QC requirements.
Extensive knowledge and expertise in cGMP compliance and quality control strategies, and industry best practices.
Strong analytical and critical thinking skills, with a solid ability to make risk based and data-driven decisions.
Excellent scientific, business, and technical communication skills, with strong cross-functional collaboration and strategic planning capabilities.
Proven ability to manage multiple priorities and thrive in a fast-paced, dynamic, and innovative environment.
Experience with global regulatory submissions, including IND, IMPD, NDA, MAA, and JNDA.

Nice To Haves

PhD in Chemistry.

Responsibilities

Manage clinical and commercial Quality Control (QC) activities from early to late phase development, process validation, commercial launch in support of RevMed’s pipeline development.
Responsible for post-approval QC related activities including commercial supplies, lifecycle management, regulatory submissions (e.g., CBE, PAS).
Partner with senior leadership on QC-related strategic development and implement QC policies and practices.
Lead the QC team, providing technical and strategic leadership for day-to-day QC activities supporting clinical and commercial programs.
Preparation for commercial product launches, management of quality events (e.g., lab investigations for OOS/OOT, deviations, CAPAs).
Direct key QC programs including stability, reference standard, raw material, QC quality systems, procedures, and documentation (e.g., SOPs), PAI readiness, and regulatory inspections.
Manage the selection, oversight, and performance management of contract organizations (COs), ensuring the effective outsourcing and execution of clinical and commercial QC activities.
Author, review, and approve QC-related documentation, including analytical methods, protocols, reports, and regulatory submissions.
Partner with cross-functional teams such as CMC Regulatory Affairs, Drug Substance, Drug Product, Supply Chain, and Quality Assurance to ensure timely achievement of project milestones and objectives.

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