15.05.24 | Vollzeit | Ludwigshafen am Rhein | PAUL HARTMANN AGProspective clinical trials, real-world data, and evidence synthesis. As part of our dynamic team, you will play a key role in contributing to protocol development, evidence synthesis, clinical risk prediction (including machinge learning modeling) and various kind of quantitative research. This role offers
Später ansehen15.05.24 | Vollzeit | Mainz | PAUL HARTMANN AGRegulation 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 and mobile working Attractive
Später ansehen15.05.24 | Vollzeit | Ludwigshafen am Rhein | PAUL HARTMANN AGControl, biocompatibility, clinical evaluation, risk management, sterilization, CE conformity, FDA, etc.) Fluent in English and German Benefits Flexible working conditions, such as flexible working hours and mobile working Attractive ways of combining work and family life, e.G. childcare subsidy 30 days
Später ansehen15.05.24 | Vollzeit | Obrigheim (Pfalz), Heidesheim | PAUL HARTMANN AGControl, biocompatibility, clinical evaluation, risk management, sterilization, CE conformity, FDA, etc.) Fluent in English and German Benefits Flexible working conditions, such as flexible working hours and mobile working Attractive ways of combining work and family life, e.G. childcare subsidy 30 days
Später ansehen15.05.24 | Vollzeit | Mainz | PAUL HARTMANN AGControl, biocompatibility, clinical evaluation, risk management, sterilization, CE conformity, FDA, etc.) Fluent in English and German Benefits Flexible working conditions, such as flexible working hours and mobile working Attractive ways of combining work and family life, e.G. childcare subsidy 30 days
Später ansehen15.05.24 | Vollzeit | Obrigheim (Pfalz), Heidesheim | PAUL HARTMANN AGRegulation 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 and mobile working Attractive
Später ansehen15.05.24 | Vollzeit | Obrigheim (Pfalz), Heidesheim | PAUL HARTMANN AGProspective clinical trials, real-world data, and evidence synthesis. As part of our dynamic team, you will play a key role in contributing to protocol development, evidence synthesis, clinical risk prediction (including machinge learning modeling) and various kind of quantitative research. This role offers
Später ansehen15.05.24 | Vollzeit | Mainz | PAUL HARTMANN AGProspective clinical trials, real-world data, and evidence synthesis. As part of our dynamic team, you will play a key role in contributing to protocol development, evidence synthesis, clinical risk prediction (including machinge learning modeling) and various kind of quantitative research. This role offers
Später ansehen15.05.24 | Vollzeit | Gierstädt | Chiesi GmbHUnd auch einmal etwas riskiert. Mit Power gehen wir die Themen an, das bedeutet für uns, mit Spaß bei der Arbeit, mit gebührendem Stolz auf Erreichtes und mit dem Herz am richtigen Fleck. Wir behalten die progressive Weitsicht, sehen Neues als Chance und schauen dabei nach links und nach rechts und reißen
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