Jeanette Roos has a diverse work experience in the pharmaceutical industry. Jeanette is currently working as a GMP GDP QA Director at Calliditas Therapeutics AB since February 2022. Prior to this, they worked at Octapharma AB for multiple roles. Jeanette was a Section Manager QA Systems & Suppliers from September 2019 to February 2022, where they were responsible for quality assurance and management within the organization. From March 2015 to September 2019, they served as a QA Manager, overseeing equipment, processes, aseptic work techniques, and cleanliness in pharmaceutical production. Jeanette also had the role of QA Manager - Change control from November 2014 to February 2015, where they coordinated and reviewed change control cases. Additionally, they worked as a Laboratory Engineer from November 2012 to November 2014, handling sample reception, sending samples for testing, and managing results and deviations. Jeanette also performed various analyses on products and was responsible for instrument and method maintenance during their tenure as a Laboratory Engineer from February 2011 to November 2012. In August 2017 to August 2018, Jeanette served as the Acting Section Manager QC Support at Octapharma AB.
Jeanette Roos has a Master's degree in Biomedical Sciences, General. Jeanette obtained this degree from both King's College London from 2009 to 2010 and Karolinska Institutet from 2006 to 2010.
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