Global Regulatory Product Planning Senior Manager - Obesity

Global Regulatory Product Planning Senior Manager – Obesity 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. The 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. Key Responsibilities Serve 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, 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. Basic Qualifications Doctorate degree and 2 years of directly related experience. Master’s degree and 6 years of directly related experience. Bachelor’s degree and 8 years of directly related experience. Associate’s degree and 10 years of directly related experience. High school diploma / GED and 12 years of directly related experience. Minimum of 2 years of experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources. Managerial experience may run concurrently with the required technical experience referenced above. Preferred 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 complex, matrixed organizations. Demonstrated ability to coordinate and align activities across multiple indications, functions, regions, and stakeholders. Experience supporting regulatory governance, business planning, portfolio planning, or strategic program management activities. Experience presenting complex information, risks, and recommendations to senior leaders and governance bodies. Proven ability to identify, assess, and mitigate risks while balancing competing priorities and evolving business needs. Experience driving organizational readiness for major regulatory milestones, health authority interactions, and business‑critical deliverables. Strong strategic thinking and problem‑solving skills with the ability to translate complex information into actionable plans and recommendations. Demonstrated ability to establish new processes, operating models, or planning frameworks within a rapidly evolving environment. Demonstrated ability to influence without direct authority and build productive relationships across regulatory and cross‑functional teams. Excellent organizational skills with a proven ability to manage multiple priorities in a fast‑paced environment. Strong written, verbal, and presentation skills. Experience utilizing planning, reporting, and visualization tools to communicate status, risks, dependencies, resource demands, and key performance indicators. Demonstrated ability to lead cross‑functional initiatives and drive organizational alignment to achieve business objectives. Salary Range 142,579.00USD – 192,901.00USD (U.S.) Equal Opportunity Employer Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. #J-18808-Ljbffr Amgen Inc. (IR)