Human Factor Engineer – pharmaceutical industry (f/m/x)

A minimum of 3 years of HF/usability professional experience or equivalent relevant experience in product development within a regulated environment; medical device experience is strongly preferred, Knowledge of FDA, ISO, IEC, AAMI, and other relevant usability standards and guidance, Strong knowledge of qualitative and quantitative research methods, Good knowledge of user-centered design practices, Experience coordinating with external consultancies, or part of an external consultancy, to conduct HF activities, Good technical writing skills, Ability to learn fast and strategically take initiative, able to work independently with minimal supervision, and a “can-do” attitude, Passion for learning, interacting with people and understanding their needs, Fluency in English, Residing in Poland required, Master’s degree in Human Factors, Usability Engineering, Biomedical Engineering, Cognitive Psychology, HCI, Anthropology or related field, Experience developing software as a medical device, digital health products and/or mobile applications within a QMS, Experience interacting with the FDA and other regulatory bodies in the context of new product approval submissions and/or audits