27.04.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGRegulatory affairs - Supporting the wider company in the maintenance and updating of documentation in accordance with relevant requirements - Ensuring product compliance to all relevant rules and guidelines Qualifications - Completed studies in natural science/engineering (e.g. medical technology, polymer
Später ansehen27.04.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGResponsibilities - Technical project support for the development and further development of medical electrical devices/systems in the field of Wound Care - Life cycle management in compliance with regulatory rules and internal processes, including preparation of technical documentation - Support in the process
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