Pharmacy Intern

Responsibilities

• Independently manage sub-projects within the European technical regulatory affairs (RA-CMC) area
• Support European and global teams with technical registration tasks
• Assist employees with regulatory submissions or authority inquiries in current global registration projects
• Handle sub-tasks in clinical study registration projects in collaboration with Clinical Research Organizations (CROs)
• Review and track the success of submissions, inform colleagues of study status, and help ensure compliance
• Conduct research on scientific and technical literature

Requirements

• Completed 2nd State Examination in Pharmacy (2. Staatsexamen in Pharmazie)
• Fluency in both German and English
• Proficiency in MS Office (Word, Excel, PowerPoint)
• Independent and team-oriented working style
• Strong communication skills
• Interest in regulatory and scientific subject matter

Preferred Qualifications

• Prior experience in the pharmaceutical industry is a plus

About the Company

Daiichi Sankyo is a global healthcare company dedicated to improving lives through innovative medicines. With a legacy dating back to 1899, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders to shape a healthier, more hopeful future for patients worldwide.