Symbios Orthopédie S.A.
Yverdon-les-Bains
11 hours ago
Quality Engineer
- 02 May 2026
- 100%
- Permanent position
- Yverdon-les-Bains
Job summary
Join Symbios as a Quality Engineer, ensuring product quality and regulatory compliance. Embrace a dynamic work environment with growth opportunities.
Tasks
- Develop quality control methods to meet Symbios' needs.
- Optimize part control processes to reduce costs effectively.
- Ensure compliance with ISO 13485 and MDR 2017/745 standards.
Skills
- Engineering degree in mechanical or microtechnology required.
- Proficient in Microsoft Office and Power BI for data analysis.
- Strong problem-solving skills with risk evaluation expertise.
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About the job
For our Quality Engineering department, we are currently looking to fill a position of
Quality Engineer
Mission
Ensure the quality of products, compliance of manufacturing processes, and patient safety, in accordance with regulatory requirements (ISO 13485, MDR 2017/745). Define, deploy and maintain effective and economically optimised quality control methods and equipment, support production and supplier management, analyse data to drive continuous improvement, and actively contribute to the overall performance of Symbios.
Responsibilities
- Develop quality control methods for Symbios' needs. Manage, qualify control equipment and validate control methods
- Optimise part control to reduce Symbios' costs. In particular by sizing quality control at Symbios by sampling and making the best use of manufacturing process control
- Ensure compliance with standards 13485:2016 and 2017/745 (MDR-EU) and any other applicable. Be an autonomous auditee / 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 first product series (FAI – First Article Inspection)
- Participate in process validations, be responsible for methodology and efficiency
- Collect and analyse production data to conclude on the need for actions necessary for continuous improvement
- Participate in technological watch
- Support engineering during the introduction of new products into production to ensure control and compliance
Profile sought
- HES engineer training (or equivalent) in mechanical or microtechnology engineering
- 3 to 5 years of experience in an engineering role in the Medtech industry.
- Good command of Microsoft Office office tools, Power BI and ease in learning new software
- Skills in Data Science, data processing, statistical analyses
- Skills in programming Python, R or other
- Perfect command of French spoken and written, and intermediate level of English (spoken and written)
- Work autonomously with a strong spirit of initiative, while closely collaborating with other departments to coordinate actions and projects.
- Be an expert problem solver, 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 cover letter, CV, diplomas and work certificates.