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- Management of Validation projects among several sites of the group
- Design of new system requirements and processes
- Issue of validation documents
- Issue of SOP dedicated to Computerized system management and validation
- Supervising the execution of tests in collaboration with business key use
- Degree in Engineering, Chemistry, or related field
- 6-12 months of experience in Computer system Validation or Pharmaceutical Quality Assurance
- Excellent knowledge of written and spoken English
- Able to work independently and collaborate effectively with higher functions and other sites
- Good team working skills and interpersonal relationships
- Ability to work under stressful conditions and meet deadlines
Global Computer System Validation Specialist - Firenze - ManpowerGroup

Descrizione
Job Title:
Global CSV Specialist
About the Role:
We are seeking a highly skilled Global CSV Specialist to join our team at Talent Solutions, part of Manpower Group, supporting an important pharmaceutical client based in Florence.
The successful candidate will be a key resource within the Global CSV team inside the Global Quality Assurance department, working collaboratively with CSV and QA representatives from company affiliates worldwide.
In this role, you will have the opportunity to work on various projects, including managing validation projects across multiple sites, designing new system requirements, and supervising test execution.
Key Responsibilities:
Requirements:
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Validation Specialist
CSV Life Science Group- Toscana
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Product Validation Specialist
Powersoft- Firenze
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Product Validation Specialist
Powersoft- Florence
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Equipment Validation Specialist
Capgemini- Firenze
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Validation Specialist - 202
TN Italy- Firenze
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Validation Specialist
Productlife Group- Firenze
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Validation Specialist - 202
Permanent contract ProductLife Group- Florence
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CQV & Process Validation Specialist - Pharma Industry
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