Director, Data Management

vor 3 Wochen


Dresden, Deutschland Arevipharma GmbH Vollzeit

For our Regulatory Affairs team , we are looking for a Head of Regulatory Affairs (m/f/d) Aufgaben Leadership Oversee and manage the Regulatory Affairs team, providing both functional and disciplinary leadership for on-site and remote employees, as well as team members across different locations and affiliates. Responsibilities Lead all regulatory processes and ensure compliance with applicable standards. Drive continuous improvement, optimization, and digitalization initiatives within the Regulatory Affairs department. Independently manage regulatory projects, consolidating data from various departments to produce regulatory reports and dossier sections. Prepare and update active substance dossiers (including QOS) following Qualifikation Candidate Profile Completed university degree (preferably as a pharmacist or chemist), ideally with a Ph.D. and a Masters in Drug Regulatory Affairs. Minimum of 5 years of experience in Drug Regulatory Affairs. Demonstrated experience in team and personnel management. Proficient in English and German (fluency required); additional languages such as French or Spanish are an advantage. Benefits Finanzielle Unterstützung Bei uns erhalten Sie verschiedene steuerbegünstigte Leistungen sowie Zuschüsse etwa zum Kita-Beitrag. Betriebliche Altersvorsorge Damit Sie im Alter abgesichert sind, zahlen wir einen höheren Zuschuss als gesetzlich vorgeschrieben. Weiterbildung Wir fördern Ihre Neugier und geben Ihnen die Möglichkeit, sich zu verschiedenen Themen weiterzubilden. Und: Getränke erhalten Sie kostenlos. Flexible Arbeitszeiten Wo möglich, können Sie Ihren Arbeitsalltag gerne flexibel gestalten.



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