- Oxford Global Resources
- Limburg
- Andere
- 13 uur geleden
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...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...
- Oxford Global Resources
- Limburg
- Andere
- 13 uur geleden
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- meer...
...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...
- Oxford Global Resources
- Limburg
- Andere
- 13 uur geleden
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- meer...
...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...
- Oxford Global Resources
- Limburg
- INT
- 1 week geleden
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...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...
...manager en een klein team. Toezicht houden op documentbeheerprocessen en ervoor zorgen dat deze voldoen aan wereldwijde en internationale normen. KPI's van het kwaliteitsmanagementsysteem (QMS) bijhou...
- Oxford Global Resources
- Noord-Brabant
- 1 week geleden
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...Regulatory Affairs Specialist who will be responsible for the end-to-end regulatory management of a portfolio of pharmaceutical products, including the preparation, submission, and maintenance of lice...
- Oxford Global Resources
- Limburg
- 1 week geleden
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...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...
- Oxford Global Resources
- Noord-Brabant
- INT
- 1 week geleden
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- meer...
...Regulatory Affairs Specialist who will be responsible for the end-to-end regulatory management of a portfolio of pharmaceutical products, including the preparation, submission, and maintenance of lice...
- Oxford Global Resources
- Limburg
- INT
- 1 week geleden
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- meer...
...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...
- Oxford Global Resources
- Noord-Brabant
- 1 week geleden
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- meer...
...Regulatory Affairs Specialist who will be responsible for the end-to-end regulatory management of a portfolio of pharmaceutical products, including the preparation, submission, and maintenance of lice...
- Oxford Global Resources
- Limburg
- 1 week geleden
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- meer...
...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...
- Oxford Global Resources
- Limburg
- INT
- 1 week geleden
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- meer...
...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...
- Oxford Global Resources
- Noord-Brabant
- INT
- 1 week geleden
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- meer...
...Regulatory Affairs Specialist who will be responsible for the end-to-end regulatory management of a portfolio of pharmaceutical products, including the preparation, submission, and maintenance of lice...
- Sysmex Netherlands & Belgium
- Noord-Brabant
- 14 uur geleden
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...Regulatory Affairs/Quality assurance. Op termijn bestaat de kans om te evolueren tot eindverantwoordelijke Je rapporteert aan de Head of Total Quality Management.Je draagt bij aan een veilige werkomge...
...Affairs (CMA) Specialist Interventional reports to the EMEA CMA Clinical Manager and is responsible for supporting the safe and effective use of the Interventional portfolio. Controleer alle bijbehore...