[Skip to main content](#main-content) [OpenNash Jobs](https://jobs.opennash.com/) [Hiring report](/reports/hiring/) · [All Revolution Medicines jobs](https://jobs.opennash.com/companies/revolution-medicines/) · [Search jobs](/search/) Revolution Medicines · Redwood City, CA # Associate Director, Analytical Development & QC Redwood City, CA Director $186,000 — $233,000 Executive & Management Listed on Revolution Medicines’s official careers site. Posted August 14, 2026. Check that it is still open and apply there. [Apply on Revolution Medicines’s careers site →](https://www.revmed.com/careers-list/?gh_jid=7806462003) [OpenNash Jobs](https://jobs.opennash.com/) / [Revolution Medicines](https://jobs.opennash.com/companies/revolution-medicines/) / Associate Director, Analytical Development & QC ## Job description Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide. Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients. ### The Opportunity Associate Director QC will be responsible for oversight of the Quality Control testing at contract labs for drug substance, drug product, and stability programs across commercial and development portfolios. Partner cross-functionally within PDM (drug substance, drug product, CMC Regulatory Affairs) and QA to manage method transfers, validations, and data oversight aligned with development and production timelines. Key responsibilities include vendor oversight, data review, external audits, and management of GMP-related exceptions (e.g., deviations, CAPAs, OOS/OOT, change controls). Oversees designation of critical quality attributes, specification setting, and trending of method and product performance. Provides direction on method transfers and validations, ensuring compliance with regulatory standards and laboratory control requirements. ### Responsibilities Lead and/or coordinate QC activities of late phase and commercial programs, including but not limited to commercial launch readiness, in-process control test, final release test, PAI readiness and inspection as needed. Oversee and manage outsourced commercial QC activities at CDMOs and/or contract testing labs (CTLs). Manage quality events related to commercial QC testing such as lab investigation (e.g., OOS/OOT), deviations, change controls (e.g., CBE 30/CBE 0) and CAPAs. Author and/or review commercial QC related documents, including methods, protocols, reports and memos. Manage commercial phase reference materials including monitoring retest date, facilitating qualification/requalification, and tracking inventory. Collaborate with cross functional teams including CMC RA, DS, DP, Supply Chain and Quality Assurance to timely achieve project goals. Coach, mentor, and engage team to ensure business goals and development plans are met. Establish and monitor operational metrics to track performance and identify trends Monitor emerging regulatory requirements and assess organizational impact. Lead remediation efforts for identified gaps and drive continuous improvement initiatives. Excellent interpersonal, negotiation, and influencing skills with the ability to manage multiple priorities and lead change across all organizational levels. ### Required Experience, Skills and Education Bachelor’s degree in a scientific discipline with 15+ years of experience in pharmaceutical QC operations across development and commercial stages. Alternatively, a Master’s degree with 12+ years or a PhD with 10+ years is acceptable. Solid understanding of relevant global and regional regulatory guidelines (FDA, EU, and ICH, etc.) as applicable to QbD, commercial process validation, commercial product launch, commercial manufacture sampling and testing, and post-approval quality control requirements. Work experience and knowledge of global regulatory submissions (IND, IMPD, NDA and MAA, etc.). Extensive knowledge and understanding of cGMP guidelines and practices, as well as related / best industry practices. Strong problem-solving skills with sound technically driven decision-making ability. ### Preferred Skills Small molecule experience is required; biologics experience is highly preferred. Effective written and verbal communication skills and interpersonal skills. 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. #LI-CT1 #LI-Hybrid The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training. Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities. Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status. Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact privacy@revmed.com. Base Pay Salary Range $186,000 — $233,000 USD We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message. Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address. If you believe you’ve been contacted by someone impersonating a Revolution Medicines recruiter, please report it to careers@revmed.com so we can share these impersonations with our IT team for tracking and awareness. ## At a glance - Posted by the employer: Aug 14, 2026 - First seen by OpenNash: Oct 11, 2026 - Last checked: Oct 18, 2026 - Listed for: 65 days - Location: Redwood City, CA - Pay: $186,000 — $233,000[Apply on Revolution Medicines’s careers site →](https://www.revmed.com/careers-list/?gh_jid=7806462003) ## More jobs at Revolution Medicines ### [Associate Director, Business Operations](https://jobs.opennash.com/companies/revolution-medicines/jobs/d85f602743a306104a91/) Redwood City, CA ### [Associate Director, Customer Master & Identity Products](https://jobs.opennash.com/companies/revolution-medicines/jobs/37a5794d18866a0603d0/) Redwood City, CA ### [Associate Director, Digital Experience Platform Lead](https://jobs.opennash.com/companies/revolution-medicines/jobs/4638a6f80a419320300e/) Redwood City, CA ### [Associate Director, Global Ergonomics & Occupational Health](https://jobs.opennash.com/companies/revolution-medicines/jobs/e44b6d870870d03a17c7/) Redwood City, CA ### [Associate Director, Portfolio Management](https://jobs.opennash.com/companies/revolution-medicines/jobs/b63a9f8b831af10b4887/) Redwood City, CA ## Similar jobs at other companies ### [Analytical Network Strategy Senior Director](https://jobs.opennash.com/companies/gsk/jobs/54b934bbdb070f43af72/) GSK · Durham, North Carolina, United States of America ### [Analytical Development Scientist (HPLC)](https://jobs.opennash.com/companies/thermo-fisher-scientific/jobs/79b7d54f975cbd327d38/) Thermo Fisher Scientific · Bedford, Massachusetts, United States of America ### [FSP - Scientist - Analytical Development Testing](https://jobs.opennash.com/companies/thermo-fisher-scientific/jobs/1bf17854c3367410973e/) Thermo Fisher Scientific · San Diego, California, United States of America ### [Associate Director, Small Molecule Analytical Development](https://jobs.opennash.com/companies/biogen-idec/jobs/2be95b759ec920951b58/) Biogen · Cambridge, MA ### [Associate Director, Antisense Oligonucleotide Analytical Development](https://jobs.opennash.com/companies/biogen-idec/jobs/f9ad952af06d434944ea/) Biogen · Cambridge, MA OpenNash lists jobs from employers’ own careers sites and does not handle applications. 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