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Business Analyst/Business Application Expert Healthcare (CSV, GxP, Sof
Eingestellt von Randstad (Schweiz) AG
Gesuchte Skills: Support
Projektbeschreibung
RANDSTAD PROFESSIONALS is currently looking for an experienced BUSINESS ANALYST/BUSINESS APPLICATION EXPERT for a great contract in Switzerland. The successful candidate will start in January 2018 and will get an initial 8 months contract with option for extension.
In order to be shortlisted for this role, you will have at least 3 years experience in the Pharma/Healthcare/Medical Device sector. Very good level of German is Mandatory.
JOB DESCRIPTION:
- 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
- Understanding of GxP/Regulatory requirements
- Independent management and tracking of TLM related projects
- Define and maintain task and KPI driven reporting
- Support CSV activities and awareness of the SD life cycle
- Understand and execute System Change Control following applicable policies and procedures
- Advanced skills with personal productivity applications (MS Word, MS Excel, flowcharting tools and Lifecycle Documentation)
EDUCATION
- Master and/or Bachelor Degree in Computer Science, Life Science OR equivalent through experience
- +3 Years of experience with projects in the pharmaceutical industry or Medical Device
- Ability to work in Matrix-organized organization/virtual teams
- Excellent communication skills in BOTH GERMAN AND ENGLISH
If your experience fits to the above description, feel free to send your application to (see below)
I am looking forward to hearing from you
In order to be shortlisted for this role, you will have at least 3 years experience in the Pharma/Healthcare/Medical Device sector. Very good level of German is Mandatory.
JOB DESCRIPTION:
- 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
- Understanding of GxP/Regulatory requirements
- Independent management and tracking of TLM related projects
- Define and maintain task and KPI driven reporting
- Support CSV activities and awareness of the SD life cycle
- Understand and execute System Change Control following applicable policies and procedures
- Advanced skills with personal productivity applications (MS Word, MS Excel, flowcharting tools and Lifecycle Documentation)
EDUCATION
- Master and/or Bachelor Degree in Computer Science, Life Science OR equivalent through experience
- +3 Years of experience with projects in the pharmaceutical industry or Medical Device
- Ability to work in Matrix-organized organization/virtual teams
- Excellent communication skills in BOTH GERMAN AND ENGLISH
If your experience fits to the above description, feel free to send your application to (see below)
I am looking forward to hearing from you
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges