Quality Engineer
We are seeking a Quality Engineer for one of our clients in the Canton of Neuchatel.
This role offers the opportunity to work in a dynamic and friendly environment in the medical devices sector.
This is an open-ended temporary contract requiring fluency in French.
Your Responsibilities:
1. Provide adequate Quality support to productions and open projects/initiatives.
2. Initiate, disposition, approve, and investigate Non-Conformances according to plans and regulatory requirements.
3. Perform quality activities for validation of new processes/products according to procedures and within defined timelines.
4. Write protocols and reports for validation documentation.
5. Perform risk analysis activities (PFMEA) according to procedures and within defined timelines.
6. Organize meetings for risk analysis activities and write risk management documentation.
7. Maintain knowledge and adherence to GMP rules on site.
8. Support QC and laboratory departments.
9. Evaluate and address quality issues in compliance with regulations.
10. Participate in internal and third-party audits/inspections.
11. Support complaint investigations if required.
12. Manage CAPA according to plans and procedures.
13. Support process improvement projects.
Your Profile:
1. Bachelor's Degree in Engineering, Life Science, or related technical discipline.
2. Experience in Medical Device manufacturing environment preferred.
3. Fluency in French and English.
4. Knowledge of Medical device standards and regulations.
5. Excellent communication, organizational, negotiation, and interpersonal skills.
6. Analytical problem-solving skills.
7. Proficiency in Agile, Oracle, EtQ, Minitab, Microsoft Office tools, and statistical techniques.