Promotional Regulatory Affairs Specialist, Europe
Core
Manage the review process for promotional and advertising assets across Europe to ensure alignment with approved labels, regulatory requirements, and internal compliance standards.
Role type
Promotional Regulatory Affairs Specialist
Builds
Promotional and advertising materials for the Europe region
Domain
Life Sciences / Ophthalmology / Regulatory Compliance
Required skills
European regulatory market knowledge, cross-functional stakeholder management, process adoption, documentation discipline, GxP compliance, medical/legal/regulatory review, compliant alternative identification
Preferred skills
Veeva, PromoMats, MAP or MLR workflows, quality/process/project management, process improvement, SOPs, ophthalmology product knowledge
Technologies
Veeva, PromoMats, MAP
Responsibilities
Manage projects for promotional and advertising assets across Spain, France, Nordics, and UK/Ireland; Review promotional, marketing, medical, and scientific materials for compliance risks; Lead MAP meetings with cross-functional stakeholders; Apply written English, French, and Spanish to review documents; Drive process adoption and continuous improvement for promotional review workflows
Seniority
Mid-level, hands-on IC
