Pharmaziepraktikant*in im Bereich Medical & Scientific Affairs /Regulatory Classics & Compliance für Mai 2028

Prepare national variations for pharmaceutical quality and informational text changes, conduct competitive environment research, and ensure data completeness through internal quality control. Manage regulatory databases and document management systems while supporting temporary regulatory projects, presentation design, and service request responses. Utilize AI-assisted tools to enhance efficiency in these tasks. This entry-level position begins in 2028 for candidates completing their second section of the pharmaceutical state exam, offering a hybrid work model up to 60% within Germany. Join Sanofi's Drug Regulatory Affairs team to contribute to market access and maintain drug approvals across Germany, Switzerland, and Austria.