Anders Bo Andersen

With over 40 years of engineering experience where-of the last 24 years in the biotech and pharmaceutical industry, I specialize in GMP, GDP, and GAMP compliance within aseptic production and cleanroom automation. My experience spans global project management and lead engineering, from documentation to large-scale biotech greenfield facilities. Entering the pharma industry with a degree in Electronics from the Air Force, I joined Flexicon where I was working in R&D developing table top and lab-size filling machines and peristaltic pumps for pharma. At Getinge Group, I established the Danish Life Science Project Department, overseeing GMP projects from conceptual design to qualification. Currently in NNE (Novo Nordisk Engineering), I serve as a Senior Specialist focusing on automated solutions for drug substance manufacturing and engineering across multiple large-scale pharma projects with focus on reducing operator impact on products through a high level of automation. Until recently, I held the chairmanship of NNE’s global Fill Finish Community of Interest, and have been involved in Bio Phorum Operational Group (BPOG) technology track for defining the requirements for future aseptic filling operations.