Pharmacy Intern

Responsibilities

• Support regulatory tasks within the German subsidiary
• Gain knowledge in centralized European authorization procedures and MRP/DCP processes
• Independently handle sub-tasks in the national phase of centralized procedures, such as updating professional and patient information
• Manage information flow to relevant departments
• Maintain regulatory-relevant databases
• Participate in global regulatory projects, such as the introduction of new process workflows
• Conduct independent research on regulatory issues within the product portfolio at national and European levels

Requirements

• Successfully completed 2nd State Examination in Pharmacy
• Interest in national and European authorization procedures and legislation
• Interest in lifecycle management of originator medicinal products
• Independent, proactive, and team-oriented working style
• Very good communication skills in German and English
• Proficiency in MS Office (Word, Excel, PowerPoint)
• Willingness to work regularly on-site in Munich

About the Company

At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. We are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders.