Jolanta graduated in Chemistry from the University of Lodz, Poland in 1997. In 2005, she gained PhD degree in organometallic chemistry under the supervision of Prof. Dr. Heinz Berke at the Institute of Inorganic Chemistry, University of Zurich, Switzerland. In 2006, she started to work as a GMP Assistant/Document assessor at Fischer Clinical Services GmbH, Allschwil. Since 2007, she joined Werthenstein Chemie AG as Engineer Quality Assurance, where she was responsible for GMP and regulatory release of secondary packaged and labelled IMPs for use in clinical studies in the EU and non-EU countries. From 2009, she became Regulatory & Compliance Manager Quality Assurance at Werthenstein BioPharma GmbH, with main responsibilities of building a new compliance & regulatory team, execution of internal audit program and writing, review, and negotiation of technical and quality agreements with third parties and inter-sites. In 2011 she joined Merck Sharp & Dohme, where she gained experience as Quality Manager, Deputy of the Responsible Person. Between 2012 and 2015, she held a position of Quality Manager, Deputy of the Responsible Person at Covis Pharma, Switzerland. She gained extensive experience in GMP release of bulk and finished drug products produced at external contract manufacturing facilities, batch release of commercial medicinal products to the US market, release of international shipments of drug substance, bulk and finished drug products according to Good Distribution Practice requirements, and much more. In 2015, Jolanta became Head of Quality Assurance, Responsible Person/Swiss QP at AbbVie AG in Baar. She is responsible for creation and maintenance of an effective Quality Management System at AbbVie AG, continuous improvement of the QMS and management of quality and compliance risks.