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

Ihr ZEISS Recruiting Team: