23.09.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGInitiatives - Lead the divisional Regulatory Affairs department, comprising a team of six members - Evaluate and define the proper regulatory strategy approach for each product - Manage, coordinate and contribute to the post-market surveillance, labeling, regulatory product documentation, conformity
Später ansehen23.09.24 | 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
Später ansehen23.09.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGInitiatives - Lead the divisional Regulatory Affairs department, comprising a team of six members - Evaluate and define the proper regulatory strategy approach for each product - Manage, coordinate and contribute to the post-market surveillance, labeling, regulatory product documentation, conformity
Später ansehen23.09.24 | 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
Später ansehen23.09.24 | 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
Später ansehen23.09.24 | 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
Später ansehen23.09.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGInitiatives - Lead the divisional Regulatory Affairs department, comprising a team of six members - Evaluate and define the proper regulatory strategy approach for each product - Manage, coordinate and contribute to the post-market surveillance, labeling, regulatory product documentation, conformity
Später ansehen23.09.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGInitiatives - Lead the divisional Regulatory Affairs department, comprising a team of six members - Evaluate and define the proper regulatory strategy approach for each product - Manage, coordinate and contribute to the post-market surveillance, labeling, regulatory product documentation, conformity
Später ansehen23.09.24 | 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
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