Job Description

In this position, you will work across multiple tasks within our growing Quality Team.

• Support site production, operations, and quality teams
• Serve as the quality representative during any product or process investigation and during external and internal audits
• Prepare and execute validations, technical studies, test method validations and other studies/reports
• Initiate and lead project teams on Corrective Action/Preventive Action (CAPA) projects
• Interface with external auditors (Notified body) during audits at the Nidau and Brügg sites; participate in the preparation and completion of corrective action plans
• Perform risk analysis, determine root cause and recommend corrective action

Your profile

• Bachelor’s degree in Quality, mechanical, life sciences or industrial engineering
• Minimum five years’ experience or advanced degree with three years of experience in quality engineering, in the medical device or pharmaceutical industries
• Excellent English skills, both spoken and written. All other languages are an asset
• Proficient IT Skills (e.g. MS Office, eQMS, etc.)
• Very flexible and adaptable to change with ability to work under pressure
• Responsible, team oriented and well-organized personality

The right decision: working at STAAR Surgical

STAAR Surgical offers you the ideal environment to develop your career and to progress professionally and personally, within a multicultural and international company. We also offer the following benefits:

• 40 working hours a week
• Modern working spaces
• Minimum 25 days of vacations
• Modern cafeteria spaces
• Monthly contribution to health insurance costs
• Training and development plans
• Free parking spaces as well as very good connections to public transportation
• Regular social company events such as summer party/winter party