What are the responsibilities and job description for the Computer System Validation (CSV) Specialist (contract) position at Capgemini?
The Computer System Validation (CSV) Specialist ensures all computerized systems in regulated industries meet stringent regulatory requirements for functionality, security, and data integrity. The role includes creating validation plans, conducting testing, documenting results, managing deviations, ensuring regulatory compliance, and providing ongoing system support. Based in Nashville, TN, this position is open to Canadian citizens eligible for a TN visa.
Visa Requirements
System Validation:
Education:
Visa Requirements
- Canadian citizens may apply; TN visa required.
System Validation:
- Ensure all computerized systems perform consistently as intended throughout their lifecycle.
- Validate system functionality, security, and data integrity in compliance with regulatory standards such as FDA, GxP, and 21 CFR Part 11.
- Develop and execute validation plans, including risk assessments, test protocols, and acceptance criteria.
- Conduct and document Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
- Create and maintain detailed validation documentation, including protocols, test scripts, validation reports, and system lifecycle documents.
- Ensure all validation activities are traceable, auditable, and meet regulatory compliance requirements.
- Identify, document, and manage validation deviations.
- Develop and implement corrective and preventive actions (CAPAs) to resolve issues and improve processes.
- Provide continuous support for validated systems to ensure they remain compliant, secure, and operational.
- Periodically review and revalidate systems as necessary to address changes in regulatory requirements or system modifications.
- Work with cross-functional teams, including IT, quality assurance, and operations, to implement and maintain validated systems.
- Provide training and guidance to end-users on validated systems and their compliance requirements.
Education:
- Bachelor’s degree in Computer Science, Life Sciences, Engineering, or a related discipline.
- Experience in computer system validation within regulated industries such as pharmaceuticals, medical devices, or biotechnology.
- Familiarity with regulatory standards, including FDA, GxP, 21 CFR Part 11, and ISO.
- Strong understanding of validation principles, system lifecycle management, and risk-based approaches.
- Proficiency in writing validation documentation, test protocols, and reports.
- Knowledge of data integrity principles and best practices.
- Strong problem-solving and organizational skills.
- Core Expertise: Computer system validation, risk-based validation, regulatory compliance.
- Industry Knowledge: FDA, GxP, 21 CFR Part 11, ISO standards.
- Soft Skills: Documentation, collaboration, training, problem-solving.
- Tools: Validation management tools, test execution software.
Salary : $25 - $40