You manage the electronic document system and support the global quality management system, ensuring effective communication and leadership across various projects and teams.
Anforderungen
- •Bachelor's degree in chemistry or engineering
- •Knowledge of FDA 21 CFR 820 and ISO 13485
- •Experience in global organizations
- •Experience in quality management for medical devices
- •Auditor training is a plus
- •Project management skills are an advantage
- •Very good English skills required
Deine Aufgaben
- •Serve as System Owner for ConSense.
- •Support global rollout of e-QMS modules.
- •Review and approve global QM documents.
- •Prepare and execute the Global Management Review.
- •Act as global interface for local QM organizations.
- •Lead global projects and indirect project teams.
Deine Vorteile
Exciting global position
Opportunity to shape quality systems
Numerous social benefits
Minimum annual salary based on group IV
Compensation based on local conditions