...Health & Safety Management (NEBOSH IDip or equivalent).GWO Basic Safety, HUET+CA-EBS, and Bi-Deltoid certifications.Offshore Medical Certificate required.🚀 Bonus: The project is offshore, heading to t...
- Oxford Global Resources
- Brussel
- 6 uren geleden
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...health care professionals to provide accurate, relevant and balanced data when needed. The Medical Advisor will develop the country medical affairs plan for 2026 and provides strategic input to intern...
- Planet Pharma
- Luik
- 6 uren geleden
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...Medical Affairs / Writing.We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, relig...
- Akkodis
- Henegouwen
- 1 week geleden
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...medical device or drug-device combination sector.Strong knowledge of international regulatory frameworks:21 CFR Part 4 / Part 820EU MDR, including Article 117ISO 13485Excellent scientific and technica...
- Akkodis
- West-Vlaanderen
- 1 week geleden
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...medical device or drug-device combination sector.Strong knowledge of international regulatory frameworks:21 CFR Part 4 / Part 820EU MDR, including Article 117ISO 13485Excellent scientific and technica...
- Akkodis
- Waals-Brabant
- 1 week geleden
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...medical device or drug-device combination sector.Strong knowledge of international regulatory frameworks:21 CFR Part 4 / Part 820EU MDR, including Article 117ISO 13485Excellent scientific and technica...
...medical device or drug-device combination sector.Strong knowledge of international regulatory frameworks:21 CFR Part 4 / Part 820EU MDR, including Article 117ISO 13485Excellent scientific and technica...
- Akkodis
- Oost-Vlaanderen
- 1 week geleden
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- meer...
...medical device or drug-device combination sector.Strong knowledge of international regulatory frameworks:21 CFR Part 4 / Part 820EU MDR, including Article 117ISO 13485Excellent scientific and technica...
- Akkodis
- Henegouwen
- 1 week geleden
- Favorieten
- meer...
...medical device or drug-device combination sector.Strong knowledge of international regulatory frameworks:21 CFR Part 4 / Part 820EU MDR, including Article 117ISO 13485Excellent scientific and technica...
...medical device or drug-device combination sector.Strong knowledge of international regulatory frameworks:21 CFR Part 4 / Part 820EU MDR, including Article 117ISO 13485Excellent scientific and technica...
- Akkodis
- Oost-Vlaanderen
- 1 week geleden
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...medical device or drug-device combination sector.Strong knowledge of international regulatory frameworks:21 CFR Part 4 / Part 820EU MDR, including Article 117ISO 13485Excellent scientific and technica...
- Akkodis
- West-Vlaanderen
- 1 week geleden
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- meer...
...medical device or drug-device combination sector.Strong knowledge of international regulatory frameworks:21 CFR Part 4 / Part 820EU MDR, including Article 117ISO 13485Excellent scientific and technica...
- Akkodis
- Henegouwen
- 1 week geleden
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- meer...
...medical device or drug-device combination sector.Strong knowledge of international regulatory frameworks:21 CFR Part 4 / Part 820EU MDR, including Article 117ISO 13485Excellent scientific and technica...
- doctoranytime Belgium
- Brussel
- 6 uren geleden
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...healthcare in Europe and Latin America. More specifically Doctoranytime's tools aim to facilitate the access to healthcare for patients and simplify the daily life of practitioners. Doctoranytime seem...
...Health Commission, etc.Required Qualifications:At least 7 years of Information Technology experience.Minimum 3 years’ experience in operating in a pharmaceutical / life sciences / medical device / hea...