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.agstaar.com. For more information, please reach out to our HR Team (032 33288 88) or visit us online at www.staar.com. jid9f6e90aa jit0310a