Nextkidney SA(www. com) is a Swiss international operating company developing Medical Devices located in Lausanne, with its head office in The Netherlands and subsidiary in Singapore. We are a fast growing innovative company developing and commercializing world’s first portable hemodialysis device. We do business in Europe, Asia, Middle East and US. You will collaborate with organizations and companies all over the world and be part of an open modern working atmosphere where business and professional human values meet. Our company

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create a better life for Dialysis patients all over the world!We are looking for a colleague in our System Department:Your

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You actively participate in performance testing for Quality Controls (QC), Design Verification activities, equipment management, and stock management activities. Key responsibilities and accountabilities :Incoming inspection:Execute test protocols in laboratory environment. Report test results and nonconformities in a timely manner. Stock management and delivery. Support the follow-up and documentation of stock moves (e. , inventory check). Support the preparation of delivery orders. Laboratory equipment management. Track the

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status of the equipment and ensure their conformity in time. Execute the equipment

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protocol, including, as applicable, sending the equipment to supplier. Maintain the corresponding documentation. Contribute to establishing work instructions/protocols, and support process improvement. System test :Execute verification test protocols as part of Design Verification. Execute characterization protocols as part of the Design and Development. Specific responsibilities :QC related tasks may be assigned (e. , contribute to investigations in the frame root cause analysis, interacting with Supplier and logistic partners). Knowledge, skills and abilities :Technical know-how for executing protocols, performing simple measurements such as weights and pressures. Familiar with quality control and quality assurance. Strong organizational skills and attention to detail. Good written written and oral communication skills. Knowledge of laboratory environment standard behaviors and

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. Attention to detail and accuracy in conducting tests. Collaborate with cross-functional teams to address and resolve quality-related issues, contributing to effective root cause analysis and corrective actions. Fluent in English, and preferably also in French. Education and experience :Technical experience in laboratory environment with relevant educational background. Experience with contributing to and executing work instructions/protocols. Experience in the field of quality in medical or another regulated industry in compliance with regulations (e. , ISO 13485, ISO 9001). Experience in the field of quality control, ideally in medical technology is a plus. Start of the

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as soon as possibleActivity rate :80-100%

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Participation to innovative projects being part of a team of experts. Access to latest technologies. A dynamic working environment where collaboration is one of the key elementsTo apply :Please send your cover letter toWrite an emailalong with your resumé. Important remarksFor this particular position, please note that only candidates possessing a Swiss passport or those fromUE-27/AELEliving in Switzerland and having a permit B will be considered for reasons of long waiting in obtaining work permits for the other candidates.

status of the equipment and ensure their conformity in time. Execute the equipment