11.09.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGIn the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance - Ideally a strong interest in and knowledge of electronic regulatory document control and management systems and associated processes - Open and competent attitude
Später ansehen11.09.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGIn the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance - Ideally a strong interest in and knowledge of electronic regulatory document control and management systems and associated processes - Open and competent attitude
Später ansehen11.09.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGIn the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance - Ideally a strong interest in and knowledge of electronic regulatory document control and management systems and associated processes - Open and competent attitude
Später ansehen11.09.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGIn the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance - Ideally a strong interest in and knowledge of electronic regulatory document control and management systems and associated processes - Open and competent attitude
Später ansehen11.09.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGIn the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance - Ideally a strong interest in and knowledge of electronic regulatory document control and management systems and associated processes - Open and competent attitude
Später ansehen11.09.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGIn the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance - Ideally a strong interest in and knowledge of electronic regulatory document control and management systems and associated processes - Open and competent attitude
Später ansehen11.09.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGIn the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance - Ideally a strong interest in and knowledge of electronic regulatory document control and management systems and associated processes - Open and competent attitude
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