...Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical device manufacturing or a rela...
- Hologic
- Vlaams-Brabant
- 1 dag geleden
- Favorieten
- 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...
...medical prescription, notarial deeds...)Intelligent apps...Your tasksProvide technical analysis based on business requirementsTake part in workload estimationDevelopment of front end and/or back end a...
- SGS Group Belgium
- Antwerpen
- Andere
- 2 maanden geleden
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- meer...
...Medical Devices Regulation (MDR), ISO 13485, MDSAP, UK Medical Devices Regulation, in overeenstemming met vastgestelde procedures en beoordelingsplannen. Deze audits kunnen zowel fysiek onderzoek ter ...
- Vivid Resourcing
- Antwerpen
- 1 maand geleden
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- meer...
...medical Sector | Antwerp RegionAre you a creative mechanical engineer with a passion for innovation and precision design?I’m currently supporting a leading biomedical organization in the Antwerp regio...
...medical prescription, notarial deeds...)Intelligent apps...Your tasksProvide technical analysis based on business requirementsTake part in workload estimationDevelopment of front end and/or back end a...
- Hologic
- Vlaams-Brabant
- 1 dag geleden
- Favorieten
- 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...
...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...
...Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical device manufacturing or a rela...
...Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical device manufacturing or a rela...
- Hologic
- Vlaams-Brabant
- 1 week geleden
- Favorieten
- meer...
...Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical device manufacturing or a rela...
- Vivid Resourcing
- Vlaams-Brabant
- 1 maand geleden
- Favorieten
- meer...
Supply Chain & Procurement Transformation Expert – FreelanceFor a medical device customer in Louvain-La-Neuve are looking for a Senior Supply Chain and Procurement Expert to join on a long term, freel...
- Vivid Resourcing
- Oost-Vlaanderen
- IT / Computing / Software
- 1 week geleden
- Favorieten
- meer...
...medical, regulated, or data-sensitive environments (not required but a plus) Experience with MicroServices, event-based architecture, or scalable backend systems Nice to have: Knowledge of medical dat...
- Hologic
- Vlaams-Brabant
- 1 dag geleden
- Favorieten
- 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
- 1 dag geleden
- Favorieten
- meer...
...Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical device manufacturing or a rela...