Quality Engineer

• 09 July 2026 • 100% • Indeterminate duration • Avenue des Trois-Lacs 26c, 1400 Yverdon-les-Bains *Symbios is a Swiss medical technology company and the leader in custom-made orthopedic implants for the hip and knee. Since its creation and relying today on 30 years of experience, Symbios has been a pioneer in the technology of custom-made implant manufacturing and has constantly improved it, thus becoming the company with the most expertise in this field worldwide.* *It employs around 270 employees 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, while respecting 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 sizing quality control at Symbios through sampling and exploiting the mastery of manufacturing processes to the best • Ensure compliance with 13485:2016 standards and 2017/745 (MDR-EU) and all other applicable ones. Be an autonomous auditor • Take charge of and coordinate investigation, correction, corrective, and preventive actions through non-conformity and CAPA processes. • Initiate, follow, 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 necessity of 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 in learning new software • Skills in Data Science, data processing, statistical analysis • Skills in programming Python, R, or other • Perfect mastery of French spoken and written, and intermediate level of English (spoken and written) • Work autonomously with a strong spirit of initiative, while collaborating closely with other departments to coordinate actions and projects. • Be a problem-solving expert, able to evaluate 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.