Pharmaceuticals
Industry and technology expertise
The pharmaceutical industry places particularly high demands on quality, process reliability, and reproducibility. In my mandates, I have supported companies in the industrialization, scaling, and stabilization of technical solutions in regulated environments—with a particular focus on manufacturing processes, automation, and quality assurance. GMP, or “Good Manufacturing Practice”, which describes the principles and guidelines of good manufacturing practice, defines the requirements for quality assurance of production processes.
A key focus of the projects was the transfer of complex products and components into robust series production under cleanroom conditions. The projects presented here show how technological precision, regulatory requirements, and economic efficiency can be successfully combined.
Technology and competence areas in the pharmaceutical environment
Product and component industrialization
Transfer of products and assemblies into series-capable manufacturing processes, taking regulatory and quality requirements into account.
Key focus areas: Industrialization, process design, and scaling.
Project management
Management of complex development and industrialization projects in regulated environments.
Key focus areas: Schedule, cost, and quality management, as well as interface coordination.
Plastic injection molding technology & manufacturing
Development and manufacturing of plastic components for pharmaceutical applications.
Key focus areas: Tooling concepts, process stability, and series production.
Automation engineering
Planning and implementation of automated manufacturing and assembly processes to ensure quality, efficiency, and reproducibility.
Key focus areas: Automation solutions, process integration, and equipment qualification.
Cleanroom applications
Design and operation of manufacturing processes under cleanroom conditions.
Key focus areas: Qualification, process reliability, and compliance with regulatory requirements.
From practice:
