Manager, Drug Product, Packaging

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Manager, Drug Product, Packaging

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 rigorall in service of patients.

The Opportunity:

Lead and oversee packaging technical transfers, packaging-line and equipment qualification activities, and packaging lifecycle management for assigned commercial products and CMO sites. This includes transfer planning and execution; packaging process, component, equipment, and line-readiness assessments; qualification and validation strategy; ongoing performance monitoring; and implementation of post-approval packaging changes, process improvements, and supply-continuity initiatives throughout the product lifecycle.

The successful candidate will serve as the primary packaging technical person for assigned CMOs, partnering cross-functionally with Quality, Supply Chain, Regulatory, Manufacturing, and external partners to manage packaging performance, investigate issues, drive continuous improvement, and maintain a state of inspection readiness.

  • Serve as the primary technical person for assigned commercial CMOs, providing day-to-day oversight of packaging operations, technical performance, and compliance.

  • Assess CMO packaging-site capability, capacity, infrastructure, and readiness to support commercial demand and future product needs.

  • Evaluate and define requirements for primary packaging components, packaging lines, inspection systems, serialization, automation, and other site-specific equipment.

  • Manage packaging technical transfers, including transfer planning, site and line readiness, process implementation, execution support, and post-transfer monitoring.

  • Manage packaging equipment and process qualification, validation, PPQ, and continued process verification (CPV) activities.

  • Manage packaging lifecycle activities, including post-approval changes, component or equipment changes, line improvements, process optimization, and supply-continuity initiatives.

  • Manage packaging-related deviations, complaints, nonconformances, investigations, root-cause analyses, CAPAs, and change controls.

  • Partner with Quality, Supply Chain, Regulatory, and CMO teams to maintain cGMP compliance, drive continuous improvement, manage documentation, and prepare for audits and inspections.

  • Support APQRs by authoring appropriate packaging sections.

Required Experience, Skills and Education:

  • Bachelor's or master's degree in Packaging Engineering, Packaging Science, or a closely related engineering discipline.

  • Approximately 68 years of relevant pharmaceutical, biotechnology, medical device, or similarly regulated industry experience.

  • Demonstrated commercial packaging experience, including responsibility for packaging operations, packaging engineering, or technical support.

  • Experience managing or providing technical oversight to external CMOs, contract packagers, or commercial packaging sites.

  • Strong knowledge of primary packaging systems, packaging equipment, line qualification, validation, PPQ, and Continuous Process Verification (CPV).

  • Working knowledge of cGMP requirements and quality systems, including deviations, CAPA, complaints, change control, and technical documentation.

  • Demonstrated ability to assess packaging-site capability, capacity, equipment needs, and operational risks.

  • Strong communication, technical writing, project-management, and cross-functional collaboration skills; willingness to travel to CMO sites as needed.

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