Beschreibung
Task:- Will need to work on the remediation of the quality system, not only as consultant, but hands-on.
- Support/train the project members onsite
Requirements (Must have):
- Relevant work experience in Quality Management /Regulatory Affairs . It should be a generalist in Quality Management
- Experience in the implementation of international regulatory processes, quality management, in compliance with DIN EN ISO 13485 and CFR 820.
- Need to have knowledge within Medical Devices or equivalent area (Pharma, Lifescience,..)
- Production-knowledge is important as well.
- CAPA Management will be part of the responsibilities and is a must have experience!
- Strong knowledge in MS Office
- Initiative, independently working manner and strong communication skills.
- Very good English and German-knowledge (spoken and written) is a must.
Beginn: 12.05.2014
Dauer: 31.12.2014
Branche: Medizin/Healthcare