Regulatory Affairs and Drug Safety Associate | Mitarbeiter:in (w/m/x) für Arzneimittelzulassung und -Sicherheit

Job Summary

This role focuses on managing regulatory processes for parallel and re-imported pharmaceuticals across the DACH region (Germany, Austria, and Switzerland). As a key member of the team, you will be responsible for preparing, submitting, and maintaining marketing authorization documents with relevant health authorities. Your daily tasks include ensuring the regulatory compliance of packaging materials, labeling, and product information, as well as communicating directly with regulatory bodies. Additionally, you will monitor legislative changes affecting the portfolio and support the pharmacovigilance department with research activities. This position is ideal for professionals seeking a secure, modern workplace in a family-run company that offers a structured onboarding process, flexible working hours, and opportunities for professional development. The blend of independent responsibility and collaborative teamwork makes this a unique opportunity in the pharmaceutical sector.