26.03.24 | Vollzeit | Grenzach-Wyhlen | naturenergie hochrhein AGUmsetzung von Maßnahmen in Zusammenarbeit mit den Betriebsteams Erstellung & Ergänzung von relevanter Dokumentation Begleitung von Schulungen, Übungen, Test & Audits im Themengebiet Sonderaufgaben, z. B. im Gebiet des Arbeitsschutzes Du bringst mit Eine abgeschlossene Ausbildung, Studium
Später ansehen09.05.24 | Vollzeit | | Schweiz | Frankreich | Michael Page InternationalRelated to compliance topics (CAPA, audit readiness) - Supports Quality Management system activities, such as CAPA, quality plans and audits - Participates in internal/external audits and inspections, and ensures that company procedures, processes and documentation meet the requirements of the Quality
Später ansehen09.05.24 | Vollzeit | | Schweiz | Frankreich | Michael Page InternationalCompliance - Develop, enhance, and document processes - Ensure timely, accurate submissions by external advisors - Document tax registration and filing across entities - Implement relevant tax tech solutions for efficiency and transparency - Manage all aspects of tax audits - Collaborate closely
Später ansehen09.05.24 | Vollzeit | | Schweiz | Frankreich | Michael Page InternationalProcesses management - - Support in post-market surveillance activities - - Medical device data management, creation and maintenance of associated documentation - - Support in QMS improvements and audits - - Ensure regulatory compliance and process optimization - - Cross-functional collaboration and advice
Später ansehen09.05.24 | Vollzeit | | Schweiz | Frankreich | Michael Page InternationalAnd invoicing. - Manage office supplies and coordinate the logistics of corporate events. - Assist in organizing sporting events and member assemblies. - Collaborate with internal and external contacts, such as auditors and financial advisors. - Ensure adherence to the association's regulations and internal
Später ansehen09.05.24 | Vollzeit | | Schweiz | Frankreich | Michael Page InternationalInitiatives to streamline and optimize the regulatory process and procedures - Contributes to the creation of regulatory strategy and plans to support the development and commercialization of new products - Participates in internal/external audits and inspections, and ensures that company procedures
Später ansehen09.05.24 | Vollzeit | | Schweiz | Frankreich | Michael Page International& external audits; - Ensure strong collaboration with other teams, and supporting them in QA/RA trainings. Anforderungsprofil - Minimum 3 years of experience within the medical device industry; - Strong knowledge of ISO 13485, ISO 14971, 21 CFR, MDR; - Experience with submitting technical files for Europe
Später ansehen09.05.24 | Vollzeit | | Schweiz | Frankreich | Michael Page InternationalWith FDA requirements - Coordinate the responses to questions raised by FDA - Review of product labelling - Participate in audits and inspections, ensuring compliance with FDA requirements - Stay up-to-date with relevant regulations, guidelines, and industry trends, and provide strategic regulatory
Später ansehen23.04.24 | Teilzeit | | Schweiz | CSL ViforExcellence (Green Belt, Black Belt, o.ä.) - Erfahrung in der Erstellung von Registrierungsdossiers - Erfahrung mit GMP Audits - Erfahrung mit spezifischen digitalen Tools (SAP, MES, PowerBi, Digital Twin, etc.) About CSL Vifor CSL Vifor aims to become the global leader in iron deficiency and nephrology. The
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