Global Regulatory Submission Planning Sr. Manager– Obesity

Career CategoryRegulatoryJob DescriptionJoin Amgen’s Mission of Serving PatientsAt Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.Global Regulatory Product Planning Senior Manager – ObesityWhat you will doLet’s do this. Let’s change the world. The Regulatory Science and Patient Safety organization is seeking a Global Regulatory Product Planning Senior Manager to support a key strategic asset within the Obesity and Related Conditions Therapeutic Area, spanning multiple indications and global regulatory activities.  This role serves as the integrated regulatory planning lead for the product, driving alignment, visibility, and execution readiness across multiple indications and all global regulatory activities.  The individual will be responsible for maintaining a comprehensive view of regulatory priorities, milestones, risks, and dependencies to support predictable regulatory execution throughout the product lifecycle. Operating within the Regulatory Business Performance Team, this role partners closely with Global Regulatory Leads (GRLs), regional regulatory leads, regulatory functional representatives, and cross-functional stakeholders to ensure the organization is prepared to meet critical regulatory objectives. This position is responsible for integrating regulatory activities across indications, functions, and regions, proactively identifying risks, and driving organizational readiness for key regulatory milestones and decisions.    As a foundational role within Amgen's growing Obesity business, the Senior Manager will help establish planning processes and execution disciplines that enable regulatory excellence at scale. This individual will provide leadership visibility into emerging risks, resource considerations, and milestone readiness while fostering alignment across a complex and evolving global regulatory environment.Key ResponsibilitiesServe as the regulatory product planning lead for a key obesity asset, maintaining an integrated view of regulatory priorities, milestones, dependencies, and risks across multiple indications.Develop and maintain a comprehensive Regulatory Product Plan that aligns regulatory objectives and activities, health authority interactions, development milestones, and major business priorities.Partner with Global Regulatory Leads (GRLs), regional regulatory leads, and regulatory functional representatives to drive alignment on key deliverables, timelines, risks, and execution strategies.Establish and maintain visibility into critical regulatory milestones, ensuring leadership has a clear understanding of readiness, risks, dependencies, and potential impacts to regulatory objectives.Facilitate regulatory planning forums to support decision-making, issue resolution, and proactive management of emerging regulatory challenges.Identify, assess, and proactively manage risks that could affect regulatory execution, working with stakeholders to develop and implement mitigation strategies.Coordinate regulatory readiness activities in support of key program milestones, major health authority interactions, and submission-related deliverables.Drive integration across indications, regulatory disciplines, regions, and cross-functional partners to ensure consistent planning and execution across the product.Partner with the Global Filing Team, Regulatory Operations, and other stakeholders to ensure alignment between strategic regulatory priorities and operational execution plans.Support resource and workload planning discussions by providing insight into upcoming regulatory demands, key deliverables, and organizational capacity considerations.Develop and maintain regulatory planning metrics, dashboards, and reporting tools that provide actionable insights to leadership.What we expect of youWe are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a leader with these qualifications.Basic Qualifications:Doctorate degree and 2 years of directly related experienceORMaster’s degree and 6 years of directly related experienceORBachelor’s degree and 8 years of directly related experienceORAssociate’s degree and 10 years of directly related experienceORHigh school diploma / GED and 12 years of directly related experienceIn addition to meeting at least one of the above requirements, you must have a minimum of 2 years of experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources.  Your managerial experience may run concurrently with the required technical experience referenced abovePreferred Qualifications:Experience supporting global regulatory activities within obesity, cardiometabolic, or related therapeutic areas.Strong understanding of global drug development and regulatory processes, including major regulatory milestones, health authority interactions, and submission requirements across key regions.Demonstrated understanding of end-to-end product development and commercialization processes and the interdependencies that influence regulatory execution.Experience developing and maintaining integrated plans within