Helps. Cares. Protects.

Join our team as a

Manager (f/m/d) Sterilization Validation - Temporary for 15 months - 

DEU-Heidenheim

 

As part of the global Sterility Assurance Team, an exciting and responsible task awaits you in a globally operating functional area. We enable our employees to get involved in interesting tasks in a modern working environment and to grow with them, as well as to develop professionally. If you are also enthusiastic about our meaningful product portfolio, we should definitely get to know each other.

 
Your area of responsibility:    

 

  • Ensuring compliance of sterilization processes and relevant technical documentation with corresponding national and international regulatory requirements
  • Preparation and implementation of Group-wide procedures and instructions for sterilization validation in compliance with current relevant national and international regulations and standards
  • Coordination and execution of sterilization process validations
  • Review and preparation of technical documentation related to sterilization processes 
  • Surveillance and auditing of internal sterilization processes of the HARTMANN Group as well as external sterilization service providers 
  • Support of the various departments (Production, R&D, Regulatory Affairs, Procurement) in projects, changes, deviations related to sterility and sterilization processes

    
What we look for:

 

  • Bachelor's or master’s degree in a scientific or technical field (medical engineering, process engineering, food technology, chemistry, pharmacy) or a comparable qualification.
  • Knowledge of the relevant European and international requirements and standards in the field of quality management and sterilization
  • Professional experience in quality management of medical devices, preferably in validation and surveillance of sterilization processes in an international company
  • Good conceptual and analytical skills for continuous improvement of processes
  • Strong communication and teamwork skills as well as a high sense of responsibility
  • Willingness to travel (worldwide)
  • Fluent in written and spoken English and German

 

Benefits:

 

  • 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. flextime or mobile working on a daily basis
  • Feedback conversations and resulting training opportunities
  • Diverse development opportunities - national and international

 

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

Helps. Cares. Protects.

Join our team as a

Manager (f/m/d) Sterilization Validation - Temporary for 15 months - 

DEU-Heidenheim

 

As part of the global Sterility Assurance Team, an exciting and responsible task awaits you in a globally operating functional area. We enable our employees to get involved in interesting tasks in a modern working environment and to grow with them, as well as to develop professionally. If you are also enthusiastic about our meaningful product portfolio, we should definitely get to know each other.

 
Your area of responsibility:    

 

  • Ensuring compliance of sterilization processes and relevant technical documentation with corresponding national and international regulatory requirements
  • Preparation and implementation of Group-wide procedures and instructions for sterilization validation in compliance with current relevant national and international regulations and standards
  • Coordination and execution of sterilization process validations
  • Review and preparation of technical documentation related to sterilization processes 
  • Surveillance and auditing of internal sterilization processes of the HARTMANN Group as well as external sterilization service providers 
  • Support of the various departments (Production, R&D, Regulatory Affairs, Procurement) in projects, changes, deviations related to sterility and sterilization processes

    
What we look for:

 

  • Bachelor's or master’s degree in a scientific or technical field (medical engineering, process engineering, food technology, chemistry, pharmacy) or a comparable qualification.
  • Knowledge of the relevant European and international requirements and standards in the field of quality management and sterilization
  • Professional experience in quality management of medical devices, preferably in validation and surveillance of sterilization processes in an international company
  • Good conceptual and analytical skills for continuous improvement of processes
  • Strong communication and teamwork skills as well as a high sense of responsibility
  • Willingness to travel (worldwide)
  • Fluent in written and spoken English and German

 

Benefits:

 

  • 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. flextime or mobile working on a daily basis
  • Feedback conversations and resulting training opportunities
  • Diverse development opportunities - national and international

 

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