Overview In this role you drive regulatory execution for North America, translating category strategies into market actions and securing timely approvals. You partner with cross-functional teams and health authorities to enable business growth while ensuring compliance. You'll lead regional regulatory delivery, lifecycle management, and risk oversight, influencing policy and innovation. This is a collaborative, impact-focused position at the cluster level with a clear pathway to shape Perrigo's self-care portfolio. Compensation / BenefitsHybrid workingTotal rewardsCareer development opportunitiesInclusive equal opportunity employerIndustry recognition (Forbes list) ResponsibilitiesDefine regional regulatory execution priorities aligned to Category strategiesTranslate regulatory strategies into actionable market plans with market insightsLead engagement with FDA and Health Canada in collaboration with Cluster HeadCoordinate with commercial, medical, quality, and policy teams to support growthEnsure submission readiness and regulatory delivery performancePartner with LCM & Regulatory Operations for post-launch lifecycle activitiesMaintain relationships with health authorities and participate in industry forumsSupport innovation pipelines and inform portfolio decisions with regulatory inputAssist business development, licensing, and M&A activitiesProvide market-specific feasibility and timing assessmentsAct as regulatory business partner to commercial teamsEnsure compliance with regulatory requirements and governance for submissions and labelingOversee regulatory vigilance and safety reporting in alignment with Global Patient SafetyLead team development and cross-functional collaboration across Regulatory, R&D, Commercial, Quality, and Medical Key requirementsDegree in Regulatory Affairs, Life Sciences, Pharmacy, or a related field12+ years of progressive regulatory affairs experience in consumer health or pharmaceuticalsProven experience leading regulatory strategy execution and market-level deliveryStrong experience with North America regulatory frameworks (FDA/Health Canada)Proven ability to be the primary regulatory interface with health authorities and manage complex submissionsStrategic partnering with cross-functional teamsStrong communication and stakeholder managementLeadership and people developmentRegulatory strategy developmentHealth authority engagement (FDA, Health Canada)Regulatory submissions and negotiations
Not specified in the original listing.
Not specified in the original listing.
