27.04.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGOf the medical device's regulation and the associated subject areas (e.g., application, design control, biocompatibility, clinical evaluation, risk management, sterilization, CE conformity, FDA, etc.) - Fluent in English and German Benefits - Flexible working conditions, such as flexible working hours
Später ansehen27.04.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGAdministration or similar - Likely to have at least 5 years' experience in a similar international role in the Med Tech - Pharma sector - Capability of reading scientific publications and understanding of the strength of reported clinical evidence - Successfully managed HTA processes in our core markets - Deep
Später ansehen27.04.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGUnderstanding of electronic, software, manufacturing processes, statistical methods, etc. - Advantageous Knowledge of Medical Devices Regulation and the associated specialist areas (e.g. application, biocompatibility, clinical evaluation, risk management, sterilisation, CE conformity, FDA, etc.) - Fluent
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