Gitte Hassan

Gitte Hassan possesses extensive experience in quality assurance and compliance within the pharmaceutical industry, currently serving as Director of QP Development and Compliance Global QA at Ferring Pharmaceuticals since January 2014. Prior to this role, Gitte worked as a QC Specialist and QP at LEO Pharma from January 2010 to December 2013, focusing on the release of raw materials and active pharmaceutical ingredients for both sterile and non-sterile production. Gitte's career in quality assurance began at Genmab, where responsibilities included the release of drug substances and products for clinical trials, management of deviations, audit processes, and regulatory documentation review from May 2008 to December 2009. Gitte holds a Master of Science degree in Pharmacy from Danmarks Farmaceutiske Universitet, obtained between 1987 and 1995.