Chloé Beck is a detail-oriented and innovative Biomedical Engineer (M.Eng.) specializing in Quality Assurance, Regulatory Affairs, and Clinical Investigation. With over six years of experience, Chloé has held various roles, including validation manager at Geistlich and quality and engineering manager at ISS AG. Prior positions include regulatory affairs officer at Laboratoires Filorga, and several internships in biomedical engineering and regulatory affairs. Chloé seeks to further develop their career within a multicultural and proactive team environment.
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