Liselotte Theorell

Liselotte Theorell has over 30 years of experience in the pharmaceutical and biotechnology industries. Liselotte began their career in 1985 as an Animal Technician at Kabi Vitrum. In 1987, they moved to Kabi as a Laboratory Engineer. In 1990, they were a Research Scientist at Kabi Pharmacia, where they were responsible for pre-clinical development of nutrition solutions. In 1994, they became Quality Assurance Manager at Pharmacia AB. From 2001 to 2008, they held the position of Quality Assurance Director at Biovitrum AB. In 2008, they became Quality Management Director at SentoClone AB, where they were responsible for GMP and GCP for Advanced Therapy Medicinal Products. From 2011 to 2014, they served as Director Quality Assurance & Regulatory Affairs at Moberg Pharma AB/Moberg Derma AB, working on both medical device products on the market and pharmaceutical projects in development. In 2014, they were the Chief Operating Officer at Cellaviva AB, a tissue establishment and biobank for stem cells. From 2016 to 2017, they were the Quality Assurance and Drug Safety Director at Pharmalink AB, where they were responsible for building quality systems. Finally, they were the Director Product Development and Quality Management at Xintela AB from 2017 to present.

Liselotte Theorell began their educational journey at Uppsala University in 1987, where they completed a field of study in Humanbiologlinjen, 80p and earned a motsv. Med kand. degree. Liselotte then moved on to Stockholm University in 1989, where they studied Kemi 40p. Lastly, they returned to Uppsala University without obtaining a degree.