My career comprises 30 years of experience within the biopharmaceutical industry and includes work assignments in Asia, South America, USA and Europe. A common denominator for my work has been to ensure a holistic and broad perspective on biomanufacturing challenges from idea to established facilities. My key focus area is to ensure fully compliant and cost-effective production through optimal use of all relevant, available knowledge and technologies, as for instance single-use systems and continuous processing. I aim to combine my technology expertise with thorough business understanding supported by a great personal interest in stakeholder relations and change management – an approach that seems to have led to success for all parties, including the involved companies, the individual employees and not least the patients, whom it is my highest wish to help best possibly. I am highly motivated by sharing knowledge and experiences in how best to meet key objectives of the pharmaceutical industry, which is why I prioritise and appreciate being actively involved in international industry organisations such as ISPE and PDA. Furthermore, I am honoured to be appointed as member of scientific committees for various international conferences, as well as member of CMC Biologics Technical Advisory Committee, PDA Biotechnology Advisory Board and Advisory Board for Master studies at Copenhagen University on Industrial Drug Development and Regulatory Affairs.Specialties: - Biopharmaceutical Manufacturing - Design of Pharmaceutical Facilities - Validation of Pharmaceutical Processes and Facilities - Single-use Systems- Continuous Manufacturing - Strategic Customer Partnership - Business Development- Change Management- Stakeholder Relations - Recognised technical presenter at international conferences- Organising and facilitator at conferences - Establishing networks and partnerships