Are you ready to go further?

At HARTMANN you get to make a difference. Our healthcare products and solutions make an impact in millions of people’s lives around the world on a daily basis – in hospitals, in clinics, and at home. We believe that health can empower people to make a positive difference in the world, and this is something worth going further for.

Join our team as a

Manager Global Quality Audits (f/m/d) - Temporary 2 years -



As part of the Global Audits Management Team, we offer you an exciting and responsible task in a globally active functional area. We offer our employees the opportunity to get involved in interesting tasks in a modern working environment and to grow and develop professionally. If you also bring along enthusiasm for our meaningful product portfolio, we should get to know each other.


Your area of responsibility:   


  • Independent planning and execution of worldwide internal audits and enforcement of quality standards
  • Planning and execution of the global audit program of the HARTMANN Group, in close collaboration with the international HARTMANN auditors team
  • Continuous development of the very well-established global audit management process 
  • Support in deriving and coordinating immediate actions, corrective actions, remedial actions resulting from global audits (Audit CAPAs)
  • Analysis of quality problems within the HARTMANN Group and development of proposals for sustainable improvement within the HARTMANN Group 
  • Analysis of processes, i.e., identification and documentation of risks, deficiencies, and potential for improvement in the area of global audits, at the units of the HARTMANN Group
  • Ensuring continuous improvement of products, processes, and production as well as compliance with existing and new global quality and regulatory requirements
  • Further development of global quality management and quality assurance systems and overarching standards for the HARTMANN Group


What we look for:


  • Bachelor or master’s degree (MBA) in business administration, IT, or comparable qualification 
  • Several years of professional experience in a comparable role in a global industrial company
  • Very good knowledge of current regulatory & cGMP requirements (EU MDR and US FDA, 21 CFR Part 820) as well as ISO 9001 & ISO 13485 standards and ISO 19011 certification desirable 
  • Strong analytical thinking and a high problem-solving competence    
  • Excellent communication and argumentation skills and stakeholder management skills
  • Team-oriented and independent work as well as a high sense of responsibility
  • Business fluent in German and English




  • Well-developed infrastructure e.g. parking bays, canteen, well-equipped workspaces
  • Furnished apartment for the first six months, if distance to place of residence > 60 km
  • Flexible working conditions, e.g. flexitime or mobile working on a daily basis
  • Diverse development opportunities - national and international
  • Feedback conversations and resulting training opportunities 
  • Various health and fitness offers, e.g. yoga during lunch break, cooperation with fitness studios, company doctor, massage offers


Please send in your application documents via our online platform to Adele Frommholz.