Backed by GV.
About the role
The Director, CMC Regulatory (post-approval) is responsible for providing strategic, hands-on and operational leadership for global post-approval submissions and CMC activities for Rasonque and other commercial products in RevMed’s portfolio. This role will lead complex global CMC lifecycle regulatory strategies across products and manufacturing sites, enabling timely execution of post-approval regulatory activities while improving submission efficiency, and simplifying regulatory processes. Found on 1752vc Careers, the job board for startup and VC roles.
What they're looking for
- Bachelor’s degree in Pharmaceutical Science, Chemistry, Chemical Engineering, or closely related scientific discipline
- Strong knowledge of US and international regulations, current industry practices, with a demonstrated ability to interpret and apply requirements for commercial products
- Strong project and team leadership capabilities, with the ability to prioritize effectively, manage multiple complex programs, and foster cross-functional collaboration
- Effective written and verbal communication skills and interpersonal skills
- A collaborative, high-energy team player who thrives in a fast-paced, dynamic environment and embraces innovation and continuous improvement
- Advanced degree (MS or Ph.D) in Pharmaceutical Science, Chemistry, Chemical Engineering, or closely related field
More about this role
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 Director, CMC Regulatory (post-approval) is responsible for providing strategic, hands-on and operational leadership for global post-approval submissions and CMC activities for Rasonque and other commercial products in RevMed’s portfolio. This role will lead complex global CMC lifecycle regulatory strategies across products and manufacturing sites, enabling timely execution of post-approval...
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