Description
AMGEN is hiring three EU Regulatory Affairs Managers to join the EU Oncology or General Medicine teams in Portugal and the United Kingdom. The role manages EU licenses and regulatory submissions for investigational and marketed medicinal products, develops regional regulatory strategies, supports product development and label negotiations, conducts regulatory research, and anticipates regulatory risks. Candidates need a degree, prior experience in a similar role, hands-on EU registration and clinical-trial experience, knowledge of EU medicinal-product legislation, strong communication skills, and basic AI-tool proficiency. Flexible work arrangements and healthcare benefits are offered.
