Job ad: QA Documentation and System Coordinator

QA Documentation and System Coordinator

Do you want to be part of a newly established cross functional team, that truly make a difference in paving the way for and lead the transition to EU Medical Devices Regulation (MDR) for our entire product portfolio?

As our new QA Document & System Coordinator, you will have a center position working closely with other highly specialised colleagues, in orchestrating the entire cycle of obtaining EU MDR approval of our products via submissions and Technical Files Audits.

Your responsibilities in the role:

• Owner of the documentation structure for the submission
• Establish and maintain documentation structures to support on-time MDR submissions
• Documentation reviews of documentation ready for submission.