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Business Process Analyst - Controlled Document Systems (4433)
Eingestellt von iET SA
Gesuchte Skills: Client
Projektbeschreibung
Our client in Basel is implementing a new clinical data system. In order to upgrade and redesign associated procesess, we are looking for a BUSINESS PROCESS ANALYST - CONTROLLED DOCUMENT SYSTEMS (4433)
YOUR QUALIFICATIONS:
- 10+ Years supporting business process mapping and system implementations for Technical Operations and Development Sciences functions, preferably in Pharma
- Proven track record of being able to apply technologies to business functions to maximize process performance
- Ability to understand technical end-user groups who have a high Programming experience
- Famliar with modern clinical data analysis system/processes
- Work background within the pharma industry is an asset
- Working understanding of GxP guidelines
- Excellent understanding of MS Office applications (Word, Excel, Visio, Project, Powerpoint)
- Fluent in English, German would be an advantage
YOUR RESPONSIBILITIES:
- Work closely with the business and technical teams
- Write the URS and contributes to the functional specifications
- Ensure that there is integration between business processes and technology solutions
- Maintain connection between (current and newly defined) business processes workflows, URS & FS
- Interpret input on business processes and write definitions & requirements that can be translated into implementation specifications for the business process management sub stream
Are you ready for a new challenge and AVAILABLE IMMEDIATELY IN BASEL? We look forward to receiving your application in MS-Word. For any questions, please contact us.
YOUR QUALIFICATIONS:
- 10+ Years supporting business process mapping and system implementations for Technical Operations and Development Sciences functions, preferably in Pharma
- Proven track record of being able to apply technologies to business functions to maximize process performance
- Ability to understand technical end-user groups who have a high Programming experience
- Famliar with modern clinical data analysis system/processes
- Work background within the pharma industry is an asset
- Working understanding of GxP guidelines
- Excellent understanding of MS Office applications (Word, Excel, Visio, Project, Powerpoint)
- Fluent in English, German would be an advantage
YOUR RESPONSIBILITIES:
- Work closely with the business and technical teams
- Write the URS and contributes to the functional specifications
- Ensure that there is integration between business processes and technology solutions
- Maintain connection between (current and newly defined) business processes workflows, URS & FS
- Interpret input on business processes and write definitions & requirements that can be translated into implementation specifications for the business process management sub stream
Are you ready for a new challenge and AVAILABLE IMMEDIATELY IN BASEL? We look forward to receiving your application in MS-Word. For any questions, please contact us.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung