18.04.24 | Vollzeit | Vaud | Randstad Schweiz AGPractices. - Ensure all analytical methodologies meet current pharmacopeial and regulatory requirements. Support filing of dossier variations - updates. - Draft - review response to queries and observation from Health Authorities. - Provide support during inspections and audits. - Participate in analytical
Später ansehen28.03.24 | Vollzeit | Lausanne | Randstad Schweiz AGContributing to the development of training materials on compliance topics. - Supporting various Quality Management System activities, including Corrective and Preventive Actions (CAPA), quality plans, and audits. Qualifications - Strong knowledge of EU Medical Device Regulation (EU) 2017/745, European
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