Torben has +20 years of experience in the pharmaceutical industry with focus on project management and validation of several inspection and assembly lines as well as packaging lines for the Packaging of Finished Goods.
Furthermore Torben has an extensive experience to the medical device industry within ISO 13485:2016 with focus at the risk management assessment within ISO14971:2019 and MDR approval of class 2 products.
As a person Torben is thorough, responsible, conscientious, broad minded and humorous and is seeking practical and simple solutions to professional challenges.
• Project management
• Writing URS
• Writing commissioning/validation documentation
• Performing commissioning/validation tests.
Packaging line for pens
• URS.
• Process FMEA.
• Risk Assessment.
• Design Qualification.
• Commissioning and validation
Novo Nordisk A/S, – 2023-present.
QMS implementation
• QMS system implementation
• Documentation package.
SPT Vilecon, Denmark – 2022-2023
