Job Description
In this position, you will work across multiple tasks within our growing Quality Team.
Support site production, operations, maintenance, calibration and quality teams
Serve as the quality representative during any product or process investigation and during external/internal audits
Prepare, execute, review and lead validations, technical studies, test method validations and other studies/reports
Lead various projects related to manufacturing activities
Support the risk management process and associated documentation applicable to STAAR Surgical AG
Initiate and lead project teams on Corrective Action/Preventive Action (CAPA) projects
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 vacation
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
If you want to contribute to the Evolution in visual freedom and become part of our passionate team, write us an email to send us your full application to: jobs.ag@staar.com .
For more information, please reach out to our HR Team (032 33288 88) or visit us online at www.staar.com .
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