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Head of Quality and Regulatory Affairs
- Medicaroid Europe GmbH
- Hibrid • Düsseldorf
- Teljes munkaidő • Kötött munkarend • Alkalmazotti jogviszony
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1-3 év tapasztalat • Angol középfok
Főbb feladatok- Cover the PRRC role when requested from the needs of the company (e.g. during the absence of the current PRRC)
- Develop and execute regulatory strategies for products and services
- Provide regulatory expertise for complex or unique issues and challenges regarding registration and compliance activities.
Március 16. -
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1-3 év tapasztalat • Angol középfok
Főbb feladatok- Provide direct line management for >10 CP Delivery Managers embedded across drug programs and AI/ML model development initiatives
- Build delivery capability through coaching, role clarity, performance management, and career development
Március 13. -
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- Teljes munkaidő • Kötött munkarend • Alkalmazotti jogviszony
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5-10 év tapasztalat • Angol középfok
Főbb feladatokAssociate Principal Scientist Dietary Supplements - Global Are you driven by advancing scientific innovation in nutrition and health? As Associate Principal Scientist Dietary Supplements – Global, you will lead the end?to?end science translation and research agenda for our Dietary Supplements...
Március 12. -
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1-3 év tapasztalat • Angol középfok • Német középfok
Főbb feladatokManagement of safety operations incl. corresponding service providers, creation and maintenance of reporting rules (in collaboration with the department Global Safety Application Management) and license partner obligations with respective compliance outputs (e.g. KPIs, PSMF)...
Március 09. -
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1-3 év tapasztalat • Angol középfok • Német középfok
Főbb feladatok- Global pharmacovigilance product responsibility for the medicinal products
- Monitoring of the benefit-risk profile
- Signal management: signal detection, signal validation, signal evaluation
- Risk management: preparation of risk management plans, supervision of risk minimization measures
Március 09. -
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1-3 év tapasztalat • Angol középfok
Főbb feladatok- Planning, writing, reviewing and submitting manuscripts on clinical drug trials in humans for peer-reviewed journals and abstracts for scientific conferences
- Data visualization of data from clinical drug trials
- Supporting preparation of posters and conference presentations
Március 05. -
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