Responsibilities:

1. 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

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Anforderungen an den Bewerber:

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

Ergänzende Informationen:

Stellenangebotsbeschreibung:

ISO 13485 Medical Device Quality Management System, Administrative ManagementIn 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!