Description

Are you from a technical background or do you come from the vice? Do you have knowledge of the MDR and ISO 13485? Do you enjoy working in a team and across departments? Do you like to take on responsibility? Would you like to ensure the regulatory saleability of stoma® products? … then we look forward to receiving your application!

Become part of our motivated team and apply as Head of Quality Management/QMBs m/f/d

  • Further development of the QM system and business processes according to Regulation 2017/745 MDR, ISO 13485 and 21 CFR 820
  • Planning, organization and execution of internal and external audits
  • Communication with authorities and notified bodies
  • responsible for management processes (CAPA, risk management, etc.)
  • Participation in the creation and maintenance of technical documentation
  • close cooperation with management and specialist departments
  • Support for Regulatory Affairs

  • Completed technical training with appropriate further training in the field of QM or a comparable degree
  • Experience in quality management for medical devices
  • good knowledge of English
  • committed, independent and structured way of working
  • team player and reliable

The succession to this responsible position is being planned with foresight: close cooperation with the current Head of Quality Management ensures that you are optimally prepared for your new role.

  • Full-time
  • Regulatory Affairs
  • Stoma / Storz am Mark GmbH
  • independent and varied area of responsibility
  • open communication, pleasant working atmosphere and short decision-making processes
  • performance-related salary
  • voluntary social benefits
  • company pension scheme
  • BusinessBike
  • flexible working hours

What makes us special s are particularly important to us. As an employer, we are committed to our employees and would be delighted if you could enrich us with your skills as part of the large stoma® team.