Jessica Köhne, ClariMed UK Senior HF Consultant - 10+ years bilingual medical device usability expert
Jessica Köhne, ClariMed UK Senior HF Consultant - 10+ years bilingual medical device usability expert
Jessica Köhne, ClariMed UK Senior HF Consultant - 10+ years bilingual medical device usability expert

Jessica Köhne

Sr. Human Factors Consultant, Manager, Site Lead Leeds UK Office

Jessica Köhne is the Sr. Human Factors Consultant, Manager, Site Lead Leeds UK Office at ClariMed. With over 10 years of experience as an Exercise Scientist and Ergonomist, she is an expert in developing Human Factors (HF) engineering strategies and leading HF activities for medical devices, from early-stage development to market support. Jessica excels in planning and moderating usability studies, preparing HF documentation for health authority submissions, and promoting human-centered design across projects. She leverages her bilingual skills and versatile experience working with diverse stakeholders to bring safe, effective, and user-friendly medical technologies to market. Jessica's analytical approach and commitment to process improvement make her a valuable asset in guiding clients through product development and regulatory compliance.

Jessica Köhne is the Sr. Human Factors Consultant, Manager, Site Lead Leeds UK Office at ClariMed. With over 10 years of experience as an Exercise Scientist and Ergonomist, she is an expert in developing Human Factors (HF) engineering strategies and leading HF activities for medical devices, from early-stage development to market support. Jessica excels in planning and moderating usability studies, preparing HF documentation for health authority submissions, and promoting human-centered design across projects. She leverages her bilingual skills and versatile experience working with diverse stakeholders to bring safe, effective, and user-friendly medical technologies to market. Jessica's analytical approach and commitment to process improvement make her a valuable asset in guiding clients through product development and regulatory compliance.

Let's work together!

Contact us to discuss how we can advance your medical device development efforts together.

Let's work together!

Contact us to discuss how we can advance your medical device development efforts together.

Let's work together!

Contact us to discuss how we can advance your medical device development efforts together.