Validation Specialist (Pharma) 100%

Vertragsart:
Vor Ort
Start:
10.2016
Dauer:
5 Monate (Verlängerung möglich)
Von:
Pidas AG
Ort:
Basel
Eingestellt:
07.09.2016
Land:
flag_no Schweiz
Projekt-ID:
1198721

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For a project with one of the world's biggest pharmaceutical companies in Basel we are looking for a motivated

Senior Computer Systems Validation Specialist

Tasks:
• Supports a global project in the manufacturing area in terms of project documentation.
• Creates and reviews GxP documentation according to PMM process and document templates
• Leads document creation together with stakeholders on QA, business and IT side and ensures approval.
• Excellent ability to communicate to others not only what is being done and how, but also why.
• Support IT and Quality while discussing CSV strategy.

Requirements:
• Recognized expert-level knowledge of relevant methodologies, technologies, languages, standards and processes with 8+ years of experience.
• Has CONDOR access and experiences to create approval workflows.
• Has proven experience working with the PMM process.

Nice to haves:
• A plus is HP ALM knowledge (project will rely on HP ALM for testing and traceability matrix).

Please sent me your cv to: