ISO 13485 Medical Device Quality Management System, Administrative Management

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

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

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!