Director of Medical Affairs for Cardiometabolic Health in Primary Care, focusing on strategic planning, medical education, and scientific exchange within the German healthcare system.

The Qualified Person (QP) is responsible for certifying that each batch of a medicinal product meets all required provisions when released from a manufacturing facility, ensuring compliance with GMP, marketing authorization, and current regulations. This role involves continuous quality and regulatory monitoring, analysis of corporate standards, participation in regulatory updates, and oversight of imported products.

This role focuses on Health Technology Assessment (HTA) strategy management within the pharmaceutical industry, specifically for the German and Austrian markets. The primary responsibilities involve developing strategies to translate evidence from clinical studies into added benefit for drug evaluations, managing the creation of dossiers according to regulatory requirements (AMNOG, EU-HTA), and coordinating with internal and external stakeholders. While the role mentions 'Digitalization/AI' as an area for process improvement, AI/ML is not the core craft of this position.