Job Description
CSV Consultant (Computerized System Validation)
In this role you will:
- Collaborate with IT stakeholders for conducting Regulatory Risk Assessment of quality systems, solutions and services
- Review validation deliverables, including Requirements Specifications (URS/FS), Test Protocols, and Final Reports
- Provide quality support for projects and application and infrastructure changes
- Support audit and inspection readiness of regulated solutions
- Guide IT stakeholders on documents and records management
- Provide recommendations to close existing compliance gaps and improve processes
- Ensure compliance to SOPs, policies and procedures
- Conduct and coordinate periodic reviews of GxP applications
- Conduct Access Roster review, Audit Trail review processes and finalize review reports
Requirements:
- CSV experience
- Familiarity with FDA regulations 21 CFR Part 11, 21 CFR Part 820, GxP...
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