Job Role - CSV Engineer
Job Location - Raritan NJ (Hybrid)
Job Details:
- 10 years experience in Computer System Validation or Quality management or Business Analysis in GxP application area
- Responsible to Author Validation Deliverables which includes - Validation / Compliance Plan Report RTM Data Flow Map Change Controls etc.
- Developing validation strategy for projects
- Providing audit support and support Application Lifecycle Management
- Managing/guiding/overseeing periodic checks
- Ability to guide cross-functional teams and mentor junior staff
- Broad experience in Computer System Validation (CSV) and testing
- Acquainted with Good Clinical Practices (GCP) regulatory requirements and FDA 21 CFR Part 11
- Clear written and verbal communication especially for technical documentation
- Acquainted with both the agile and waterfall software development methodology
- Solid understanding of the fundamentals of iterative and incremental software development
- Proficiency in tools like JIRA qTest SNOW and/or other validation tracking systems
- Skilled in project planning execution and minimal rework strategies
- Capable of risk identification and mitigation especially in regulated environments
- Strong Analytical and Problem solving
Job Role - CSV Engineer Job Location - Raritan NJ (Hybrid) Job Details: 10 years experience in Computer System Validation or Quality management or Business Analysis in GxP application area Responsible to Author Validation Deliverables which includes - Validation / Compliance Plan Report RTM Da...
Job Role - CSV Engineer
Job Location - Raritan NJ (Hybrid)
Job Details:
- 10 years experience in Computer System Validation or Quality management or Business Analysis in GxP application area
- Responsible to Author Validation Deliverables which includes - Validation / Compliance Plan Report RTM Data Flow Map Change Controls etc.
- Developing validation strategy for projects
- Providing audit support and support Application Lifecycle Management
- Managing/guiding/overseeing periodic checks
- Ability to guide cross-functional teams and mentor junior staff
- Broad experience in Computer System Validation (CSV) and testing
- Acquainted with Good Clinical Practices (GCP) regulatory requirements and FDA 21 CFR Part 11
- Clear written and verbal communication especially for technical documentation
- Acquainted with both the agile and waterfall software development methodology
- Solid understanding of the fundamentals of iterative and incremental software development
- Proficiency in tools like JIRA qTest SNOW and/or other validation tracking systems
- Skilled in project planning execution and minimal rework strategies
- Capable of risk identification and mitigation especially in regulated environments
- Strong Analytical and Problem solving
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