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Business Analyst: Pharmaceutical, J&J, German, GxP, TLM, CSV
Eingestellt von Sentinel IT LLP
Gesuchte Skills: Support
Projektbeschreibung
Business Analyst: Pharmaceutical, J&J, GERMAN, GxP, TLM, CSV
A world renowned Johnson & Johnson owned company in Switzerland is seeking a Business Analyst who speaks fluent English and German. The successful candidate will have a very strong pharmaceutical background (ideally with J&J experience).
Primary Tasks and Responsibilities:
*Focus on improvements on the overall application landscape in alignment with the strategic and tactical guidelines
*Oversee and manage the application portfolio and roadmaps in alignment with line manager
*Maintain high level of quality, related to regulatory and compliance policies and guidelines
*Independent management and tracking of TLM related projects
*Define and maintain task and KPI driven reporting
*Support computerized system validation activities and understand the SD life cycle
*Understand and execute System Change Control following applicable policies and procedures
*Understanding of GxP/Regulatory requirements
*Advanced skills with personal productivity applications such as MS Word, MS Excel, flowcharting tools and Lifecycle Documentation
*Master and/or Bachelor Degree in Computer Science, Life Science OR equivalent through experience
*+3 Years of experience with projects in the pharmaceutical industry
*Ability to work in Matrix-organized organization/virtual teams
*Excellent communication skills in both German and English
A world renowned Johnson & Johnson owned company in Switzerland is seeking a Business Analyst who speaks fluent English and German. The successful candidate will have a very strong pharmaceutical background (ideally with J&J experience).
Primary Tasks and Responsibilities:
*Focus on improvements on the overall application landscape in alignment with the strategic and tactical guidelines
*Oversee and manage the application portfolio and roadmaps in alignment with line manager
*Maintain high level of quality, related to regulatory and compliance policies and guidelines
*Independent management and tracking of TLM related projects
*Define and maintain task and KPI driven reporting
*Support computerized system validation activities and understand the SD life cycle
*Understand and execute System Change Control following applicable policies and procedures
*Understanding of GxP/Regulatory requirements
*Advanced skills with personal productivity applications such as MS Word, MS Excel, flowcharting tools and Lifecycle Documentation
*Master and/or Bachelor Degree in Computer Science, Life Science OR equivalent through experience
*+3 Years of experience with projects in the pharmaceutical industry
*Ability to work in Matrix-organized organization/virtual teams
*Excellent communication skills in both German and English
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges