Your Role
1. purpose of the job is to contribute and support maintenance and effectiveness of CZM’s Quality Management System in compliance with regulatory requirements, quality strategy and business needs
2. executing governance as well as taking on a moderating role about internal QMS requirements
3. the function drives best practice sharing across the organization and ensures best fit of the QMS for business
Your Profile
4. Bachelor or Master’s degree, preferably in scientific/technical studies or business administration or equivalent work experience in combination with another degree
5. at least 5 years proven experience in Quality Management or Regulatory Affairs in the medical device industry
6. strong knowledge of statutory and regulatory requirements that apply to medical device industry (e.g. ISO 13485, MDR)
7. methodological and task-specific qualifications (e.g. internal auditor)
8. knowledge on implementing management and internal control systems including their monitoring
9. conceptual strength, open "out-of-the-box" thinking and experience in the coordination of cross-disciplinary collaboration
10. working knowledge of collaborative tools (e.g. SharePoint, Teams, etc.)
11. passion for management systems, cross-department intercultural teamwork and the willingness to travel
12. strong communication, networking and analytical skills as well as the ability to handle conflicts
13. a high level of commitment and outstanding initiative; objectivity in your work Very good written and spoken English
Your ZEISS Recruiting Team:
Marina Löw