Director, GPS Quality & Compliance

Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Our Global Patient Safety (GPS) organization is seeking a Director, GPS Quality & Compliance to support our quality event management and inspection readiness programs. This role partners closely with the Senior Director, GPS leadership, Global Development Quality, and the QPPV Office, and operates as a functional leader who coordinates and delegates work across the team to ensure consistent, high-quality program delivery.  This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. When & where: •    Location: Warren, NJ (preferred), Armonk or Tarrytown, NY, or Cambridge, MA •    Work model: 4 days/week on-site •    Travel percentage: 20% with some fluctuation expected based on onsite audit/inspection support needs. Discover your role: •    Lead functional workstreams across quality event management and inspection programs, coordinating and delegating work across a team •    Serve as a trusted point of contact during GCP and GVP audits and inspections, guiding teams through preparation and real-time response •    Bring order to complexity by maintaining inspection readiness materials and translating regulatory frameworks into practical action •    Champion a culture of accountability and continuous improvement, acting as an escalation point when issues arise •    Turn data into direction, reviewing quality metrics and trend analyses to shape clear, actionable recommendations for senior leadership •    Communicate with confidence and clarity, presenting governance topics and quality insights to senior team members •    Lead through influence, coordinating across teams and functions regardless of formal reporting lines This role requires: •    A Bachelor's degree required; advanced degree preferred with a minimum of 12 years of pharmaceutical industry experience; Healthcare Professional background preferred •    Deep knowledge of global PV regulations, quality management systems, and inspection readiness frameworks (FDA CFR, GVP Modules) •    Demonstrated experience facilitating FDA and EMA/MHRA inspections (GCP and GVP), including direct experience as an inspection point of contact •    Proven track record overseeing QMP governance, metrics programs, and cross-functional quality oversight •    Experience managing relationships across GDQ, QPPV Office, Regulatory Affairs, and vendors •    People management experience preferred   Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all  qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.   Where necessary, we disclose salary ranges for roles in all countries in which we operate.  The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.