System Technician

Next Kidney SA is a fast-growing innovative company developing and commercializing the world’s first portable hemodialysis device. We do business in Europe, Asia, and US. You will collaborate with investment funds (VC’s), foundations and companies all over the world and be part of an open modern working atmosphere where business and professional human values meet.

Our company mission: create a better life for Dialysis patients all over the world!

As a System Technician, you actively participate in performance testing for Quality Controls (QC), Design Verification activities, equipment management, and stock management activities.

• Execute test protocols in laboratory environment.
• Report test results and nonconformities in a timely manner.

• Support the follow-up and documentation of stock moves (e.g., inventory check).
• Support the preparation of delivery orders.

• Track the qualification status of the equipment and ensure its conformity in time.
• Execute the equipment qualification protocol, including, as applicable, sending the equipment to supplier.
• Maintain the corresponding documentation.
• Contribute to establishing work instructions/protocols, and support process improvement.

• Execute verification test protocols as part of Design Verification.
• Execute characterization protocols as part of the Design and Development.

QC related tasks may be assigned (e.g., contribute to investigations in the frame root cause analysis, interacting with Supplier and logistic partners).

• 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 and oral communication skills.
• Knowledge of laboratory environment standard behaviors and requirements.
• 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.

• 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.g., ISO 13485, ISO 9001).
• Experience in the field of quality control, ideally in medical technology is a plus.

As soon as possible.

80-100%.

• 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 elements

Please send your cover letter to ... along with your résumé.

For this particular position, please note that only candidates possessing a Swiss passport or those from UE-27/AELE.