Manager quality engineering Jobs in Essingen

Your Role

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

executing governance as well as taking on a moderating role about internal QMS requirements

the function drives best practice sharing across the organization and ensures best fit of the QMS for business

Your Profile

Bachelor or Master’s degree, preferably in scientific / technical studies or business administration or equivalent work experience in combination with another degree

at least 5 years proven experience in Quality Management or Regulatory Affairs in the medical device industry

strong knowledge of statutory and regulatory requirements that apply to medical device industry (e.g. ISO 13485, MDR)

methodological and task-specific qualifications (e.g. internal auditor)

knowledge on implementing management and internal control systems including their monitoring

conceptual strength, open "out-of-the-box" thinking and experience in the coordination of cross-disciplinary collaboration

working knowledge of collaborative tools (e.g. SharePoint, Teams, etc.)

passion for management systems, cross-department intercultural teamwork and the willingness to travel

strong communication, networking and analytical skills as well as the ability to handle conflicts

a high level of commitment and outstanding initiative; objectivity in your work Very good written and spoken English

Your ZEISS Recruiting Team :

Marina Löw