Beschreibung
For our customer in Solothurn we are looking for a project for a Sterility Assurance Specialist 100% (f/m)
Main Activities:
Know and follow all laws and policies that apply to ones job, and maintain the highest levels of professionalism, ethics and compliance at all timesDiligently participate in our client's compliance program-related activities as denoted by your supervisor or our client's Chief Compliance OfficerResponsible for managing the EU reprocessing cleaning programWork with PD to ensure initial product concepts will fit into the Synthes Sterility Assurance (SA) systemProvides SA oversight to ensure the adequacy of these activities and documentation in terms of regulatory compliance and technical soundness throughout the European manufacturing system. This should be accomplished by working closely with Product Development (PD).Work with PD to ensure timely and complete adoptions and validations of all new products with regard to sterilization and cleaningTrain PD personnel in basic sterilization and in sterilization procedures if applicableCorrespond with customers with special requests regarding the sterilization/cleaning programEnsures compliance to the applicable Medical Device Directive (MDD), ISO 13485 and FDA (QSR) regulations as they apply to sterilization and reprocessing cleaningKnowledge of the Robert-Koch- Institute guidelines, ISO 15883, ISO 17665, and ISO 17664 are required and knowledge of AAMI standards/reports a plusOthers responsibilities as given by Sterility Assurance EURequirements:
At least 5 years of experience with reprocessing (eg hospital, CSSD, etc)Open to understand reprocessing in different countriesKnowledgeable in applicable Medical Device Directive (MDD), ISO13485, ISO 14971, ISO 9001 and FDA (QSR) regulationsWell versed in government regulations and industry guidelines for sterilization (ie ISO/EN/AAMI standards: Robert-Koch-Institute Guidelines, ISO 15883, ISO 17665, ISO 17664)This position requires a high level of written and oral communication skills Working knowledge of applicable software, particularly Microsoft Office applicationsExcellent organizational skills and multi-tasking abilitiesVocational qualification plus at least 5 years practical experience and supplementary on-going professional training or Qualification from college or higher education plus 3 years practical experienceAre you interested in this position? Then we are looking forward to receiving your application. Please contact me if you have any further queries
