Executive Director of Regulatory Affairs - Obesity and Related Conditions (Thousand Oaks)

Career CategoryRegulatoryJob DescriptionJoin Amgen’s Mission of Serving Patients At 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. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity-related conditions.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.Executive Director of Regulatory Affairs & Obesity Related ConditionsWhat you will doLet’s do this. Let’s change the world. In this vital role as Executive Director of Regulatory Affairs, you will direct regulatory affairs activities within an assigned disease area, ensuring compliance with applicable laws and regulations. You will also provide strategic direction and leadership to the regulatory affairs team.The Executive Director of Regulatory Affairs is a product facing cross-indication regulatory integration role that leads a designated part of the Obesity and Related Conditions Global Regulatory Therapeutic Area in the Global Regulatory Affairs organization. This role ensures strategic coherence, alignment, and risk management across multiple products with concurrent indications and global filings.This role will report into the Vice President, Global Regulatory Affairs.Responsibilities:Lead, coach, and mentor staff to develop a high-performing regulatory organization grounded in continuous learning, with a strong focus on talent development, leadership capability, and a succession planning culture.Build strong alignment across global and regional teams ensuring clarity of purpose, priorities and coordinated executionGuide integrated cross-indication regulatory strategy across Obesity programs, ensuring alignment of development pathways, evidence generation, and global registration approachesProvide strategic regulatory expertise and guidance to therapeutic area commercialization teams and other governance bodiesAct as a trusted strategic partner to Global Regulatory Leaders (GRLs) providing guidance on complex regulatory decisions, risk management, and long-term strategyConduct management review and approval of Global Regulatory Strategic PlansConduct review and approval of key documents for regulatory submissionsAnticipate and translate the evolving regulatory landscape within therapeutic area into forward looking regulatory strategies and opportunitiesWork externally to influence regulatory legislative environment in line with Amgen policy priorities for the therapeutic areaOversee and participate in licensing/acquisition due diligence and other activities in partnership with Amgen licensing groupsCommunicate and ensure alignment of global functional and cross-functional goals and objectivesKnowledge and skills include:Demonstrated experience leading complex, multi-indication regulatory strategy integrationDemonstrated ability to lead teamsStrong communication skills - both oral and writtenAbility to understand and communicate scientific informationComprehensive understanding of regulatory activities and how they affect projects and processesDemonstrable ability to set organizational direction & champion change and continuous improvementProven ability to anticipate and mitigate against future strategic issues & uncertaintiesAbility to resolve conflicts and develop a course of action leading to a beneficial outcomeProven ability to drive enterprise-level alignment under high portfolio complexityWhat we expect of youWe are all different, yet we all use our unique contributions to serve patients. The executive candidate we seek is an experienced leader with the following qualifications.Basic Qualifications:Doctorate degree & 6 years of regulatory affairs experience ORMaster’s degree & 10 years of regulatory affairs experience ORBachelor’s degree & 12 years of regulatory affairs experience AND6 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resourcesPreferred Qualifications:Demonstrated leadership of regulatory strategy for programs in obesity, metabolic disorders, endocrinology, cardiovascular risk, or related therapeutic areas.They will also embody the Amgen leadership attributes which are:Inspire: Create a connected, inclusive, and inspiring work environment that empowers talent to thriveAccelerate: Enable speed that matches the urgency of patient needs by encouraging progress over perfectionIntegrate: Connect the dots to amplify the collective power of Amgen to drive results for patients, staff, and shareholdersAdapt: Lead through change by adapting to an ever-changing environment and defining a clear course of action to deliver resultsWhat you can expect of usAs we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is $255,302 - $345,408. Actual salary will vary based on several factors including, but not limited to, relevant skills, experience, and qualifications.In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.A discretionary annual bonus program, or for field sales representatives, a sales-based incentive planStock-based long-term incentivesAward-winning time-off plans and bi-annual company-wide shutdownsFlexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.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 with 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..Salary Range255,301.75USD -345,408.25 USDSummaryLocation: US - California - Thousand OaksType: Full time