Quality Manager/Documentation Specialist
We are working with a Biotech start-up who design, develop and produce hardware/software solutions for the medical and pharmaceutical industries. Due to success and an increase workload, they now have a vacancy for a Quality Manager/Documentation Specialist to join them on a permanent basis at their offices near Zurich.
In this role you will be responsible for electronic document management system. You will be developing, maintaining and improving the ISO 9001 and ISO 13485 quality management system.
- Excellent experience and knowledge with ISO 9001 and ISO 13485 standards
- Previous experience working or managing a Quality Management System
- Experience in the Medical/Pharmaceutical industries
- Quality Management
For more information, please click apply and someone will be in touch to discuss in more detail.