Associate Director, CMC Regulatory

OpenKrill; United States; Remote; USD 177,000 - 221,000; Full time

Job summary

Revolution Medicines seeks an Associate Director, CMC Regulatory to lead global CMC regulatory strategies supporting clinical development, regulatory submissions, and lifecycle management of the company’s oncology portfolio. You will chair cross‑functional teams, prepare CMC sections for IND/NDA/MAA submissions, and ensure compliance with GMP requirements worldwide.

The role requires strong experience in CMC regulatory affairs, excellent communication, and the ability to drive timelines in a

Qualifications

• BA/BS in Pharmaceutical Science, Chemistry, Chemical Engineering, or closely related field.
• 10+ years of pharmaceutical/biotech drug development experience with 5+ years in global CMC regulatory affairs.
• Experience in CMC global submissions (IND, IMPD/CTA, NDA, MAA, etc.) (US, EU, APAC, LATAM).
• Knowledge of US and international GMP quality regulations.
• Experience with CMC development of NCEs (small molecules).
• Ability to prioritize multiple projects in a dynamic, global environment.

Responsibilities

• Develop, lead and implement global CMC regulatory strategies to support clinical development, registration, and post‑marketing activities.
• Lead the preparation and maintenance of CMC/quality sections for regulatory submissions (IND, IMPD/CTA, NDA, MAA, etc.).
• Serve as the CMC regulatory representative on project teams and support development and lifecycle management of products.
• Collaborate with regulatory teams, CMC SMEs and CROs to identify regional CMC requirements and drive submission timelines.
• Provide regulatory assessment and guidance on CMC changes, deviations and investigations.
• Contribute to internal process improvements and SOP development to support globalization of RevMed’s products.

Skills

Communication skills

Cross-functional collaboration

Project management

Regulatory strategy

Regulatory submissions

Education

BA/BS in Pharmaceutical Science or related field

Advanced degree (MSc/PhD) desirable

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:

As part of our expanding organization, we seek a strategic and hands‑on Associate Director, CMC Regulatory who will be responsible for executing CMC regulatory strategies to support clinical development, marketing authorizations, and lifecycle management of RevMed’s pipeline compounds/products.

Responsibilities:

• Develop, lead and implement global CMC regulatory strategies to support the clinical development, registration, and post-marketing activities.
• Lead the preparation and maintenance of the CMC / quality sections for regulatory submissions including initial submission of IND, IMPD/CTA, NDA, MAA and amendments to Health Authorities (HAs), and preparation of responses to queries from HAs.
• Serve as the CMC regulatory representative on project teams and provide CMC regulatory support for the development of the investigational product(s) and marketed products and ensure applicable regulatory requirements are appropriately met.
• Collaborate with corporate regulatory team, CMC SMEs and/or CROs to identify regional/country-specific CMC requirements to support global applications, and to drive the CMC submission timelines in order to meet business objectives.
• Provide regulatory assessment and guidance on CMC related change controls, deviations, and investigations throughout product life cycle.
• Lead and/or contribute to internal process improvements, SOP development, and organizational initiatives to support globalization of RevMed’s products.Maintain knowledge of global competitive landscape, regulatory environment, regulations and CMC guidance, providing interpretation to internal stakeholders.

Required Skills, Experience, and Education:

• BA/BS degree in Pharmaceutical Science, Chemistry, Chemical Engineering, or closely related field.
• 10+ years of pharmaceutical / biotech drug development experience with 5 + years of experience of global CMC regulatory affairs.
• Experience in CMC related global submissions (IND, IMPD/CTA, NDA, MAA, etc.) (US, EU, APAC, LATAM).
• Solid knowledge of US and international GMP quality regulations, current industry practices, and experience with interpretation and application to development projects and marketed product regulatory issues.
• Working experience and content knowledge in CMC development of NCEs (small molecules) or equivalent.
• Demonstrated experience in effective collaboration with internal and external stakeholders.
• Ability to prioritize and manage multiple projects simultaneously in a dynamic company environment.
• Ability to operate effectively in a fast-paced, matrixed, global environment.
• Effective written and verbal communication skills and excellent interpersonal skills.

Preferred Skills:

• Advanced degree (MSc or PhD degree) in Pharmaceutical Science, Chemistry, Chemical Engineering, or closely related field is desirable.
• Experience in accelerated development program.
• Self‑driven, proactive, and able to operate independently while fostering collaboration across departments.

#LI-CT1 #LI-RemoteThe 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 [e-mail].

Base Pay Salary Range$177,000-$221,000 USD