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Technical Document Writer/Tester
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Engineering, Library
Projektbeschreibung
Harvey Nash is looking for a Technical Document Writer/Tester/Validation Specialist for a 9 month project in Switzerland.
The role is for a candidate for the creation of technical specifications, gathering of reference data, software testing and validation.
You are responsible for
- Validation according to CSV 5.0
- Testing
- Gathering of reference data
- Test case creation
- Creation of technical documentation
- Statistical evaluation/analysis
- Other tasks in terms of REMIS project
Requirements
- Experience in specifying, configuring, testing and documenting of systems and applications
- Testing experience
- Validation, CSV 5.0 knowledge
- Good technical understanding with good networked thinking
- German and English fluent
- Statistical evaluation/analysis know how would be advantageous
- Degree in informatics or engineering
- 2-5 years of project related experience in pharma manufacturing
- You are self-reliant, resilient, flexible and open minded
- Esp. experience with PMM and with the tools involved for maintaining a project (Perform, Clarity, Project Library, etc.) is a big plus; project Experience
- Good communication skills
- Experience in Manufacturing Execution Systems (MES)
- Experience in Manufacturing Intelligence Solution (MIS)
Are you available immediately, have experience working within a Life Science company? Please send your complete CV (Word documents preferred) to (see below) For further details feel free to call me. I am looking forward to receiving your application.
The role is for a candidate for the creation of technical specifications, gathering of reference data, software testing and validation.
You are responsible for
- Validation according to CSV 5.0
- Testing
- Gathering of reference data
- Test case creation
- Creation of technical documentation
- Statistical evaluation/analysis
- Other tasks in terms of REMIS project
Requirements
- Experience in specifying, configuring, testing and documenting of systems and applications
- Testing experience
- Validation, CSV 5.0 knowledge
- Good technical understanding with good networked thinking
- German and English fluent
- Statistical evaluation/analysis know how would be advantageous
- Degree in informatics or engineering
- 2-5 years of project related experience in pharma manufacturing
- You are self-reliant, resilient, flexible and open minded
- Esp. experience with PMM and with the tools involved for maintaining a project (Perform, Clarity, Project Library, etc.) is a big plus; project Experience
- Good communication skills
- Experience in Manufacturing Execution Systems (MES)
- Experience in Manufacturing Intelligence Solution (MIS)
Are you available immediately, have experience working within a Life Science company? Please send your complete CV (Word documents preferred) to (see below) For further details feel free to call me. I am looking forward to receiving your application.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Ingenieurwesen/Technik