Managing change execution and change Coordination in the area of Global External Manufacturing with internal stakeholders (e.g. Quality Management) and external contract manufacturers
Responsible for the efficient implementation of changes within the company and also at the the contract manufacturer
Responsible for compliance application of the change and the corresponding KPIs
Responsible for maintenance and preparation of the regulatory correct documentation, for example Change Request/Change
Notification, Design Master Record, Design History File etc
Planning and implementation of projects and work packages from product care projects with minimal supervision
Being a proactive member of the squad
Identification of process improvements in the working area (e.g. change process)
Profile
B.Sc. degree in Engineering, Natural Science or related disciplines or apprenticeship with high degree of subject matter expertise
Initial Project management experience
Work experience in change management or in project and process management
Practical experience in a regulated GxP environment, ideally in medical devices/IVD industry (ISO 13485, FDA 21 CFR 820, IVDR/MDR)
First professional experience in document management within a regulated environment
Good knowledge in SAP or comparable ERP system
Very good user skills in MS Office and Google applications
Very good communication skills in German (B1) and English (C1) (spoken and written) are required
Team player, independent and reliable way of working is expected
Benefits
Fascinating, innovative environment in an international atmosphere