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Validation Software Facilitator

Illinois  ‐ Onsite
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Keywords

Description

Responsibilities
Provide for the Computerized System Life Cycle Compliance for validated and non-validated computerized systems, web and mobile applications, and websites.
Review and Approval of SLC Deliverables
Validation Master Plan (creation and updates)
Computerized System Periodic Reviews per the Validation Master Plan
21 CFR Part compliance
Quality Assurance Library activities (physical library maintenance activities.)

SKILLS:

Must have experience in Pharma and with the GxP regulations
Start date
n.a
From
Synectics
Published at
16.09.2014
Project ID:
775272
Contract type
Freelance
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