| Computer System Validation (Pharma) - (Ver detalles de Oferta) |
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| Amaris Consulting | Madrid, Community of Madrid, es | 2026-04-13 - |
| Develop and maintain system-specific SOPs and SLC documentation. Manage validation status throughout system lifecycle and post-operation phases. Experience with LeVA system life cycle documentation (VP, URS, FS, RA, Testing Reports, AAP). - Amaris Consulting |
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| Computer system validation consultant - (Ver detalles de Oferta) |
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| Rephine | Madrid, Community of Madrid, es | 2026-04-11 - |
| Your Role:
As a CSV L2 Consultant, you will take an active role in delivering high-impact validation projects, with a focus on ERP systems and other critical computerized systems in regulated environments. Who We're Looking For:
Are you passionate about consulting in the Pharma and Life Sciences sec - Rephine |
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| Computer system validation (pharma) - (Ver detalles de Oferta) |
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| Amaris Consulting | Madrid, Community of Madrid, es | 2026-04-12 - |
| WHAT WOULD YOU NEED?
+3 years of senior experience in IT validation within Gx P environments
Proven expertise in Veeva Conformance and Validation Testing and W3 C Validation
Strong knowledge of pharma industry regulations and Gx P compliance
Experience with Le VA system life cycle documentation (VP - Amaris Consulting |
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| Computer System Validation (CSV) Lead - (Ver detalles de Oferta) |
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| Discover International | es | 2026-03-10 - |
| Computer System Validation within Life Sciences. Computer System Validation (CSV) Lead. Experience validating enterprise applications, digital platforms or data systems. - Discover International |
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| Computer System Validation (Pharma) - (Ver detalles de Oferta) |
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| Amaris Consulting | Madrid, Community of Madrid, es | 2026-04-10 - |
| WHAT WOULD YOU NEED? ??
~+3 years of senior experience in IT validation within GxP environments
~ Proven expertise in Veeva Conformance and Validation Testing and W3C Validation
~ Strong knowledge of pharma industry regulations and GxP compliance
~ Experience with LeVA system life cycle docum - Amaris Consulting |
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| Computer System Validation (CSV) Lead - Spain - (Ver detalles de Oferta) |
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| Discover International | es | 2026-03-10 - |
| Computer System Validation (CSV) Lead. Computer System Validation within Life Sciences. Lead validation activities for digital platforms and enterprise systems. - Discover International |
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| Computer system validation (pharma) - (Ver detalles de Oferta) |
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| Amaris Consulting | Madrid, Community of Madrid, es | 2026-04-12 - |
| Lead validation activities for global testing applications (BI-AS-ODIN, BI-IT-INMATION)
Ensure compliance with validation planning and applicable BI standards before system operation
Develop and maintain system-specific SOPs and SLC documentation
Manage validation status throughout system lifecycle - Amaris Consulting |
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| Computer System Validation (CSV) Lead - Discover International - (Ver detalles de Oferta) |
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| Discover International | es | 2026-03-10 - |
| Computer System Validation (CSV) Lead. Computer System Validation within Life Sciences. Experience validating enterprise applications, digital platforms or data systems. - Discover International |
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| Computer System Validation (Pharma) - (Ver detalles de Oferta) |
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| Amaris Consulting | Madrid, Community of Madrid, es | 2026-04-11 - |
| WHAT WILL YOU DO? &##128072;
Lead validation activities for global testing applications (BI-AS-ODIN, BI-IT-INMATION)
Ensure compliance with validation planning and applicable BI standards before system operation
Develop and maintain system-specific SOPs and SLC documentation
Manage validation status - Amaris Consulting |
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| Computer System Validation (Pharma) - (Ver detalles de Oferta) |
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| Amaris Consulting | Madrid, Community of Madrid, es | 2026-04-06 - |
| Experience with LeVA system life cycle documentation (VP, URS, FS, RA, Testing Reports, AAP). Degree in Business Administration, Computer Science or comparable professional experience. Ensure compliance with validation planning and applicable BI standards before system operation. - Amaris Consulting |
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| Computer System Validation (Pharma) - (Ver detalles de Oferta) |
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| Amaris Consulting | Madrid, Community of Madrid, es | 2026-03-15 - |
| Develop and maintain system-specific SOPs and SLC documentation. Manage validation status throughout system lifecycle and post-operation phases. Experience with LeVA system life cycle documentation (VP, URS, FS, RA, Testing Reports, AAP). - Amaris Consulting |
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| Computer System Validation (Pharma) - (Ver detalles de Oferta) |
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| Amaris Consulting | es | 2026-02-27 - |
| Experience with LeVA system life cycle documentation (VP, URS, FS, RA, Testing Reports, AAP). Degree in Business Administration, Computer Science or comparable professional experience. Ensure compliance with validation planning and applicable BI standards before system operation. - Amaris Consulting |
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| Computer System Validation (Pharma) - Amaris Consulting - (Ver detalles de Oferta) |
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| Amaris Consulting | es | 2026-04-01 - |
| Degree in Business Administration, Computer Science or comparable professional experience. Ensure compliance with validation planning and applicable BI standards before system operation. Develop and maintain system-specific SOPs and SLC documentation. - Amaris Consulting |
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Inscribirse
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| Computer System Validation (Pharma) - (Ver detalles de Oferta) |
 |
| Amaris Consulting | es | 2026-03-10 - |
| Degree in Business Administration, Computer Science or comparable professional experience. Ensure compliance with validation planning and applicable BI standards before system operation. Develop and maintain system-specific SOPs and SLC documentation. - Amaris Consulting |
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Inscribirse
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| Computer System Validation (Pharma) - (Ver detalles de Oferta) |
 |
| Amaris Consulting | es | 2026-04-01 - |
| Experience with LeVA system life cycle documentation (VP, URS, FS, RA, Testing Reports, AAP). Degree in Business Administration, Computer Science or comparable professional experience. Ensure compliance with validation planning and applicable BI standards before system operation. - Amaris Consulting |
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Inscribirse
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