As complaint handling specialist for medical devices you are responsible for the structured investigation of claimed products.
You will do device inspection and root cause analyses on these claimed products and based on your findings initiate corrective actions if necessary.
Moreover you analyze engineering data, test certificates, risk evaluations, etc. and compile trendings. Your results are then documented in English in the international Stryker database.
You successfully completed your studies in a technical field (ideally mechanical engineering, quality management or medical technology) or alternatively you have completed your technical apprenticeship above-average and have already gained some work experience in a regulated environment.
Ideally, you already have first experiences in complaint handling of medical devices (post market vigilance) and have had experience with the implementation of corrective actions (CAPA).
You have a distinctive passion for technical matters, are an analytical thinker and like to work independently but also in interdisciplinary teams.
Very good written and spoken English complete your profile. German and/or French is a plus.