Quality Engineer

Quality Engineer Symbios is a Swiss medical technology company, and the leader in custom orthopedic implants for the hip and knee. Since its creation and relying on 30 years of experience, Symbios has been a pioneer in the technology of custom implant manufacturing and has constantly improved it, becoming the company with the greatest expertise in this field worldwide. It employs around 270 collaborators across Europe, including more than 200 based at its headquarters in Yverdon-les-Bains. For our Quality Engineering department, we are currently looking to fill a position of Quality Engineer Mission Ensure the quality of products, the conformity of manufacturing processes and patient safety, in compliance with regulatory requirements (ISO 13485, MDR 2017/745). Define, deploy and maintain high-performance and economically optimized quality control methods and equipment, support production and supplier management, analyze data to drive continuous improvement, and actively contribute to Symbios' overall performance. Responsibilities Develop quality control methods for Symbios' needs. Manage, qualify control equipment and validate control methods Optimize part control to reduce Symbios' costs. Notably by dimensioning quality control at Symbios through sampling and making the best use of manufacturing process control Ensure compliance with standards 13485:2016 and 2017/745 (MDR-EU) and all other applicable standards. Be an autonomous auditor Take charge of and coordinate investigation, correction, corrective and preventive actions through non-conformity and CAPA processes. Initiate, monitor and implement changes through the Change Control process Qualify suppliers and initial product series (FAI - First Article Inspection) Participate in process validations, guarantee methodology and efficiency Collect and analyze production data to conclude on the need for actions necessary for continuous improvement Participate in technological monitoring Support engineering during the introduction of new products into production to ensure mastery and compliance Sought profile HES engineer training (or equivalent) in mechanical engineering or microtechnology 3 to 5 years of experience in an engineer role in the Medtech industry. Good mastery of Microsoft Office tools, Power BI and ease of learning new software Data Science skills, data processing, statistical analysis Programming skills, R or other Perfect mastery of French spoken and written, and intermediate level of English (spoken and written) Work autonomously with a strong sense of initiative, while collaborating closely with other departments to coordinate actions and projects. Be a problem-solving expert, able to assess risks, propose relevant solutions and make informed decisions in the interest of the company. If this challenge interests you, we look forward to receiving your complete application file with CV, diplomas and work certificates. jpid929d62fjm jit0728jm jiy26jm