Dr. Carsten Heil

Having a broad knowledge in most life science topics, Carsten focuses on engineering excellence in regulated environment with a clear focus on efficiency, (cyber)security, agility and reg. compliance. In his career, he worked in both, consulting positions and line management for large, global medical device manufacturers Carsten understands the industry from overall regulations to detailed technical implementations. Besides processes and tools, Carsten has experience in development and production of medicinal products and medical devices, infrastructure for collection and processing of clinical data but also in implementation and validation of ERP and MES systems. Even if Carstens focus is on engineering, he covers all MD regulations but also regulations for pharm. production and logistics.