-
- Teljes munkaidő
-
1-3 év tapasztalat • Angol középfok
Főbb feladatokProviding strategic regulatory guidance developing global regulatory strategy, planning and execution of global investigational and marketed prescription drug submissions and managing lifecycle regulatory activities in alignment with the Therapeutic Area Lead under the direction of the Senior...
Március 19. -
Head of Quality and Regulatory Affairs
- Medicaroid Europe GmbH
- Hibrid • Düsseldorf
- Teljes munkaidő
-
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. -
- Teljes munkaidő
-
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. -
Design Quality Engineer – New Product Development
- Acrostak (Schweiz) AG
- Stegackerstrasse 14
- Teljes munkaidő
-
5-10 év tapasztalat • Nem kell nyelvtudás
Főbb feladatokDesign Quality Engineer – New Product Development About the Role Department: Quality Assurance Reports to: QMR / Head of Quality Acrostak is a global leader in health technology, committed to improving hundreds of thousands of lives worldwide and striving to make the world healthier and more...
Március 10. -
- Teljes munkaidő
-
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. -
- Teljes munkaidő
-
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. -
- Teljes munkaidő
-
3-5 év tapasztalat • Angol középfok • Német középfok
Főbb feladatokGlobal Scientific Manager - IBU Critical Care Become part of a vital chain and contribute to our common goal of making people’s lives better. Headquartered in Lachen, Switzerland, Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced...
Február 25.
-
Head
-
Of
-
Development
-
Egészségügy, Gyógyszeripar
-
Minőségbiztosítás