- 3-7 years of hands-on experience in computer system validation and understanding of CSV lifecycle & regulatory expectations.
- Validation experience in pharmaceutical, life sciences with regulatory and compliance environment
- Knowledge of 21 CFR part 11, EU Annex 11 and GAMP
- Experience in facing audits such as USFDA, WHO, EU, GLP/ GMP, and other inspection bodies is preferable.
: The role primarily involves:
- Identifying the vulnerabilities, performing risk assessment, and implementing the procedures for computerized system for effective mitigation controls.
- Manage and support for validation of Computer system, both new implementation and for existing including plans, protocols, and reports.
- Executing periodic validation/verification of computerized system.
- Ensuring overall compliance and maintaining the lifecycle documentation for GxP computerized systems as per valuable documentation practices.
- Assisting the IT-administrator in managing his/her roles and responsibilities.
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📌 System Engineer (Delhi)
🏢 SHRIRAM INSTITUTE FOR INDUSTRIAL RESEARCH
📍 Delhi
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