Tasks
* Checking and creating various QMS documents
* Officialization of the documents
* Maintenance of the document training matrix
* Training and advising employees on QM issues (filing the Q system, training, document control, documentation review, test plan creation, etc.)
* Review and approval of simplified qualification documentation
* Accompanying, processing and evaluating error messages
* Collaboration on various projects
Profile
* Basic technical or commercial training with a flair for business management or technical matters
* Knowledge of quality management (ISO 9001 or ISO 13485), ideally further training in quality management (SAQ, NDS)
* Very good written and spoken German and English skills
* Sound knowledge of MS Office
* Experience in medical technology or pharmaceuticals an advantage
* High quality awareness and appropriate working methods
* Stamina, resilience and flexibility
* Enjoy working in a team and also repetitive tasks
We offer you an exciting challenge in the growth-oriented medical technology market. As a committed and proactive personality, you can play a formative role in the future of our dynamic company. Have we aroused your interest? Then we look forward to receiving your complete online application with CV, letter of motivation, references and diplomas.
For further information, please contact Mr. Richard Büchi, Director Human Resources ,
If you have any technical questions, please contact Ms. Anna Kohler, CO-Director Quality Management & Regulatory Affairs, tel