Orbe, Vaud, Switzerland
Career objectives Manage a Quality, R&D department or large-scale projects within a well-known Medical Device company. Act as representative in front of customers, partners, competent authorities and other external parties. Promote Quality and Good Practices in the whole company; actively contribute to objectives achievements; Provide benefits of skills and experience previously acquired. Skills summary Manage R&D, Quality Assurance & Regulatory departments. Acting as Site Manager following an acquisition, manage transfer of activities and integration of products. Manage complex projects since early phases of the development up to Medical Device launch in the market. Establish, maintain and improve full Integrated Management System and more specifically in the Medical Device field (ISO 13485, 21 CFR part 820). Conduct improvement projects by applying recognized methods. Leadership confirmed in international, multidisciplinary and multicultural organizations.