Judith Kairies is experienced within regulatory affairs and quality assurance in the life science industry. She has worked with pharma, medical devices and in vitro diagnostics, as well as healthcare.
Judith’s career started as a certified biomedical laboratory engineer where she worked in different clinical laboratories but mostly within clinical chemistry. She went on to complete a master within bio-entrepreneurship at Karolinska Institutet and to work as a consultant within regulatory affairs placed at AstraZeneca. Following her passion for diagnostics, Judith finally switched to PlantVision AB where she works as a regulatory affairs and quality assurance consultant within medical devices and in vitro diagnostics and where she specializes within EU’s in vitro diagnostic regulation (IVDR). Since she started at PlantVision AB, Judith also provides courses and organizes events within the subject.
An example of events Judith has organized is Swedish Labtech’s IVDR summit 2021. Next to working at PlantVision AB Judith has also been active as a board member in associations such as Biotech-Hanse and Apotekarsocieteten. Today Judith has the position of Teamlead at PlantVision AB, where she is responsible for a team of consultants active within regulatory affairs and quality assurance in the in vitro diagnostic industry.
