15.05.24 | Vollzeit | Lachen (SZ) | Estée Lauder AG LachenOf Safety, health, hazardous Materials, machinery Safety, or Environmental Affairs, preferably in manufacturing operations - Preferred certifications Specialist for Occupational Safety and Health (ASGS), NEBOSH International Diploma, Certified Safety Professional (CSP) or similar designations or working
Später ansehen16.05.24 | Vollzeit | Michael Page InternationalMain navigation Looking for advice? Language English Search Job title Location Sort by [Relevance_] Salary Min [Salary min] Salary Max [Salary max] Regulatory and Quality Assurance Specialist Switzerland Interim - Save Job - Added 03/04/2024 - You have experience in regulatory affairs - You
Später ansehen06.05.24 | Vollzeit | Courroux | Randstad Schweiz AGAnd Visio. Preferred, but not required skills include - Experience with eQMS (Trackwise or similar). - Experience as a QP or QP substitute. - Experience in regulatory Affairs
Später ansehen28.03.24 | Vollzeit | Lausanne | Randstad Schweiz AGAre you ready to dive into the world of Regulatory Affairs and Quality Assurance ? We're on the lookout for a RA & QA Compliance Specialist to join a dynamic team and medical device company ! We are seeking a qualified candidate for the role of Regulatory Affairs and Quality Assurance Specialist
Später ansehen08.03.24 | Vollzeit | careers.tecan.comLeading and organizing Task Forces resulting from investigations to initiate or accompany short-term corrective actions. - Assessing deviations regarding reporting obligations in cooperation with the Global Complaint Unit and Regulatory Affairs based on investigation results. - Implementing the Quality
Später ansehen03.11.19 | Vollzeit | Zürich | SygnumCompliance Officer to join our Executive Board. About you - Are you passionate about Compliance and Regulatory Affairs? - Are you passionate about finding solutions and inspiring others? - Are you passionate about blockchain and digital assets? - Are you keen to work in a dynamic, fast-moving
Später ansehen31.10.19 | Vollzeit | Bern | DecomplixYou bring - a technical background and enjoy writing technical documents; - professional experience in quality management or regulatory affairs in the Medtech industry; - detailed knowledge of ISO 13485 and the certification processes for medical devices in Europe, ideally for software-only products
Später ansehen28.10.19 | Vollzeit | Zürich | headcount AGOur client is a top 20 Pharma company with their headquarters in the German speaking region of Switzerland. They are currently recruiting three (Senior) Directors, heading up their Regulatory Affairs Strategy teams. These will be your tasks \ Oversee global/regional regulatory leads and staff
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