What are the responsibilities and job description for the Regulatory Affairs Director position at 3DISC?
Job Description:
This role will require you to oversee the development and implementation of design control processes and ensure compliance with FDA and international regulations. You will be responsible for maintaining a Quality Management System and conducting internal audits to identify areas for improvement.
The ideal candidate will have a strong background in medical device quality management and regulatory affairs, as well as experience in CAPA, remediation projects, and internal audits.
This role is an exciting opportunity to join a global leader in the medical device industry and contribute to the development of cutting-edge intraoral scanners.
