Director Public Policy - Science and FDA Policy

Director of Policy & Government Affairs – Science and FDA Policy As the Director of Policy & Government Affairs for Science and FDA Policy, you will lead Regeneron’s science and FDA policy portfolio, developing, shaping and influencing government and multinational organization policy related to the scientific research and development of biopharmaceutical medicine and cell and gene therapy across the product lifecycle. The role focuses on product approval standards and pathways, scientific ethics and integrity, clinical trial activity, evidence development, manufacturing and CMC criteria, biosimilars, and other relevant science policy issues. Key Responsibilities Engage with internal subject‑matter experts and leaders to understand Regeneron’s business and corporate interests, recognize policy risks and opportunities, and determine short and long‑term policy objectives to navigate competing interests. Communicate policy positions and initiatives to internal and external audiences through various channels, and organize and participate in events, conferences, and forums to promote Regeneron’s agenda. Represent the PP&GA team at key stakeholder meetings and engage external partners to identify collaboration opportunities for shared policy priorities. Engage with industry associations, advocacy groups, and other external stakeholders to build coalitions and advance shared policy objectives. Develop and advance strategic public policy positions and initiatives that align with Regeneron’s business objectives. Monitor and analyze legislative and regulatory developments at the federal, state, local, and international levels to assess potential impact on Regeneron. Develop and execute strategic advocacy plans, including crafting and vetting legislative and regulatory proposals to advance company priorities and mitigate risks. Provide expert advice and guidance on policy and regulatory matters to internal stakeholders. Qualifications Bachelor’s degree (required); advanced degree in Public Policy, Political Science, Law, or related field with a science background strongly preferred. Minimum of 12 years of relevant experience in science and regulatory policy, preferably with substantial at‑US FDA experience. Proven record of successfully crafting and influencing public policy and navigating complex and highly technical issues. Strong understanding of the biopharmaceutical industry, including regulatory and legislative processes. Benefits Health and wellness programs (medical, dental, vision, life, disability insurance). Fitness center access, 401(k) with company match, family support benefits, equity awards, annual bonuses. Paid time off and paid leaves (e.g., military and parental leave). EEO Statement Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief, sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation for known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company’s business. #J-18808-Ljbffr Regeneron Pharmaceuticals, Inc (USA)