- British School Of Brussels
- Brussel / Vlaams-Brabant
- Andere
- 1 week geleden
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...medical conditions in students to all staff and update appropriately. Organise and implement first aid and other health/medical programmes for staff and sport/activity coaches. Work with teaching staf...
- Barry Callebaut
- België
- Human Resources
- 2 weken geleden
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.../or issues you will be an important advisor and support to an Operation Manager and his/her direct reports. About you Education: A bachelor's or master's degree in HSE, environmental science, safety, ...
- Hologic
- Vlaams-Brabant
- 2 weken geleden
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.../IVDR, CFR820, ISO 13485, Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical devi...
- Hologic
- Vlaams-Brabant
- 3 weken geleden
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- meer...
...medical device manufacturing or a related industry, with 5+ years in a Quality Auditing function preferred. Working knowledge of Medical Device Regulations/In Vitro Diagnostic Regulation, cGMP, CFR 82...
.../IVDR, CFR820, ISO 13485, Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical devi...
- Hologic
- Oost-Vlaanderen
- 3 weken geleden
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.../IVDR, CFR820, ISO 13485, Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical devi...
.../IVDR, CFR820, ISO 13485, Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical devi...
.../IVDR, CFR820, ISO 13485, Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical devi...
- Hologic
- Vlaams-Brabant
- 3 weken geleden
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- meer...
.../IVDR, CFR820, ISO 13485, Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical devi...
- neuroClues
- Waals-Brabant
- 3 weken geleden
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...medical device industry.Excellent analytical and problem-solving skills.Strong communication and interpersonal skills.Knowledge of FDA regulations and ISO 13485 quality standards.Ability to manage mul...
.../IVDR, CFR820, ISO 13485, Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical devi...
- Hologic
- Vlaams-Brabant
- 4 weken geleden
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- meer...
...medical device manufacturing or a related industry, with 5+ years in a Quality Auditing function preferred. Working knowledge of Medical Device Regulations/In Vitro Diagnostic Regulation, cGMP, CFR 82...
- Hologic
- Vlaams-Brabant
- 4 weken geleden
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- meer...
...medical device manufacturing or a related industry, with 5+ years in a Quality Auditing function preferred. Working knowledge of Medical Device Regulations/In Vitro Diagnostic Regulation, cGMP, CFR 82...
- Hologic
- Vlaams-Brabant
- 2 weken geleden
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- meer...
...medical device manufacturing or a related industry, with 5+ years in a Quality Auditing function preferred. Working knowledge of Medical Device Regulations/In Vitro Diagnostic Regulation, cGMP, CFR 82...
- Hologic
- Vlaams-Brabant
- 2 weken geleden
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- meer...
...medical device manufacturing or a related industry, with 5+ years in a Quality Auditing function preferred. Working knowledge of Medical Device Regulations/In Vitro Diagnostic Regulation, cGMP, CFR 82...