Senior Director of Regulatory Affairs - North America

We have an exciting new role within our Global Perrigo Scientific Office. As the newly appointed Senior Director of Regulatory Affairs - North America, your role will sit within the Cluster Regulatory Affairs pillar, where you will be responsible for in-market execution and regulatory delivery. Category Regulatory Affairs owns ideation-to-launch strategy, regulatory pathways, and global dossier expectations; this role provides market input and executes the agreed strategy locally. LCM & Regulatory Operations owns regulatory classification governance, post-launch lifecycle activities (non-innovation), and operational processes and systems; and this role sets market priorities and delivery expectations. Final submission sign-off is owned by Markets in partnership with Category Regulatory Affairs; this role leads readiness, execution, and regulatory recommendation. Degree in Regulatory Affairs, Life Sciences, Pharmacy, or a related field. 15+ years of progressive regulatory affairs experience within consumer health, pharmaceuticals, or adjacent sectors Demonstrated experience in leading regulatory strategy execution and delivery at market or regional level, including health authority interactions. Strong experience with North America regulatory frameworks (e.g., FDA and/or Health Canada), or equivalent regional expertise where applicable. Proven ability to act as the primary regulatory interface with health authorities, including managing complex submissions, negotiations, and issue resolution. Strong business acumen with the ability to partner effectively with commercial and cross-functional stakeholders to enable growth. #J-18808-Ljbffr Perrigo Company plc