ISO 13485 Medical Device Quality Management System, Administrative Management (Qualitätsmanager/in)

Responsibilities:

• Responsible for conducting ISO 13485 system audits, organizing internal audits, and management reviews. Dealing with customer audits, external audits, and liaising with third-party organizations. 1.
• Human resource management, human resource planning, performance evaluation, personnel system, employee training, and training on laws and regulations related to medical devices. Good communication skills, able to self motivate and motivate the team. 1.
• R&D project management, customer email processing, and daily operation management 2.
• Provide short-term business travel management guidance in Shenzhen, China

Ergänzende Informationen:

Anforderungen an den Bewerber: Erweiterte Kenntnisse: Büro- und Verwaltungsarbeiten, Qualitätsaudit, Qualitätsmanagement, Dokumentation (technisch), Personalplanung, Projektmanagement

In the initial phase, you work 2.5 days a week! Time: Every Monday, every Tuesday, 0.5 days randomly. After that, adjust the working hours and salary as the workload increases!