Louise has 15 years of experience within the biopharmaceutical industry. Starting with GMP Cell bank production and early Upstream process development in small scale bioreactors, gaining valuable experience in process development and GMP. She has 4 years of experience within Quality Assurance (QA), supporting operation/production with batch review, change management, deviations(SME), CAPA, releasing cell banks and in general supporting production compliance.
Louise has been instrumental in startup of a pharmaceutical company playing a key Project Manager role setting up the production facility, including, procedures, qualification FAT/SAT, IOQ, PQ according to SRV strategy. With her solid compliance mindset and structured approach, Louise often takes up a key role in supporting our clients.
