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German-Speaking Startup Site Manager
- Grafton Recruitment
- Távmunka / Remote
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1-3 év tapasztalat • Angol felsőfok • Német felsőfok
Főbb feladatok- Manage regulatory submissions and site start-up activities for clinical trials in Germany
- Prepare and review site regulatory documentation, ensuring completeness and compliance
- Negotiate site contracts and budgets with clinical trial sites
Április 01. -
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1-3 év tapasztalat • Angol felsőfok
Főbb feladatokScientific oversight and coordination of preclinical and toxicology studies conducted in collaboration with CROs, academic partners, and scientific institutions - covering both GLP-regulated and exploratory/non‑GLP research...
Március 30. -
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- Teljes munkaidő • Kötött munkarend • Alkalmazotti jogviszony
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1-3 év tapasztalat • Angol középfok • Német anyanyelvi szint
Főbb feladatokLead Expert Quality Assurance, Deputy Responsible Person 40% 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...
Március 23. -
- Teljes munkaidő • Kötött munkarend • Alkalmazotti jogviszony
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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 • 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. -
Qualified Person (QP) - (m/w/d)
- Lilly
- Németország
- Teljes munkaidő • Kötött munkarend • Alkalmazotti jogviszony
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1-3 év tapasztalat • Angol felsőfok • Német felsőfok
Főbb feladatok- Confirms, certifies, and releases batches of products manufactured, ensuring all manufacturing steps have been performed in compliance with GMP, the marketing authorization of the relevant product, defined procedures, and current regulations.
- Confirms batches of products intended for clinical trials.
Március 10.
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Finance controller
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Manager
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Egészségügy, Gyógyszeripar
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Törzskönyvezés