Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Senior Computer System Validation (CSV) IT Pharma
Eingestellt von Edelway
Gesuchte Skills: Support, Natural, Client
Projektbeschreibung
Edelway is a Swiss consultancy active in the field of Pharma and IT.
We are actively looking for a Senior Computer System Validation(CSV) consultant to join our global pharmaceutical client in Neuchâtel, Switzerland.
The Role:
* You'll support quality management and CSV activities on IT projects and programs.
* This will include conducting quality reviews of IT systems and processes, writing, reviewing and approving the required documentation and ensuring compliance with regulations, standards and clients' quality management systems.
* You will review technical writing; support PowerPoint presentation etc.
* With a keen eye for details, you'll identify errors or deficiencies in IT systems and processes and drive their continuous improvement.
* Writing, reviewing and implementing IT procedures, processes and working instructions will also be part of your role.
* You'll support testing, documentation and change management activities as well as risk assessments and risk mitigations.
Your profile:
* Educational background in IT, Business, Natural Sciences or Engineering
* At least 4 years of hands-on work experiences in quality management and CSV or another quality assurance area within the pharmaceutical industry
* Some experience Computer System Validation activities on GxP IT projects/systems
* Good knowledge of Microsoft Office tools (Word, Visio, Project, Excel, PowerPoint, SharePoint)
* Experiences in working on IT projects and programs within multicultural, global or virtual project teams
* Good business communication and presentation skills, fluency in English
If this sounds like your next challenge, send me your CV at (see below)
Keywords: CSV, validation, IT, system, GxP, compliance, regulations
We are actively looking for a Senior Computer System Validation(CSV) consultant to join our global pharmaceutical client in Neuchâtel, Switzerland.
The Role:
* You'll support quality management and CSV activities on IT projects and programs.
* This will include conducting quality reviews of IT systems and processes, writing, reviewing and approving the required documentation and ensuring compliance with regulations, standards and clients' quality management systems.
* You will review technical writing; support PowerPoint presentation etc.
* With a keen eye for details, you'll identify errors or deficiencies in IT systems and processes and drive their continuous improvement.
* Writing, reviewing and implementing IT procedures, processes and working instructions will also be part of your role.
* You'll support testing, documentation and change management activities as well as risk assessments and risk mitigations.
Your profile:
* Educational background in IT, Business, Natural Sciences or Engineering
* At least 4 years of hands-on work experiences in quality management and CSV or another quality assurance area within the pharmaceutical industry
* Some experience Computer System Validation activities on GxP IT projects/systems
* Good knowledge of Microsoft Office tools (Word, Visio, Project, Excel, PowerPoint, SharePoint)
* Experiences in working on IT projects and programs within multicultural, global or virtual project teams
* Good business communication and presentation skills, fluency in English
If this sounds like your next challenge, send me your CV at (see below)
Keywords: CSV, validation, IT, system, GxP, compliance, regulations
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
IT Entwicklung, Sonstiges