CSV Engineer

Computer System Validation (CSV) Engineer

We are seeking a Computer System Validation (CSV) Engineer with experience in Computer System Validation (CSV) within a GMP-regulated pharmaceutical or biotechnology environment. The ideal candidate will have expertise in GAMP 5, 21 CFR Part 11, validation lifecycle documentation, and QC laboratory or manufacturing systems validation, while collaborating with cross-functional teams to ensure regulatory compliance.

Roles & Responsibilities:

• Develop, execute, and maintain Computer System Validation (CSV) documentation and validation protocols for QC laboratory systems and manufacturing systems.
• Support the complete validation lifecycle, including preparation, execution, review, and approval of User Requirements Specifications (URS), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Risk Assessments, and Validation Reports.
• Perform risk assessments to identify and mitigate validation and compliance risks.
• Ensure compliance with GAMP 5, 21 CFR Part 11, GMP, and internal quality standards.
• Review validation documentation to ensure accuracy, completeness, and regulatory compliance.
• Collaborate with Quality Assurance (QA), Manufacturing, Engineering, and IT teams to support validation activities and system implementations.
• Provide validation support for QC laboratory systems and manufacturing equipment throughout their lifecycle.
• Assist with change control, deviation investigations, and periodic reviews related to validated systems.
• Maintain accurate validation records and ensure documentation is audit ready.
• Support internal and external regulatory inspections by providing validation documentation and technical expertise.

Requirements:

• Bachelor's degree in engineering, Computer Science, Life Sciences, Pharmacy, Biotechnology, or a related field.
• Experience in Computer System Validation (CSV) within a GMP-regulated pharmaceutical or biotechnology environment.
• Strong knowledge of GAMP 5, 21 CFR Part 11, and GMP regulations.
• Hands-on experience supporting QC laboratory systems and/or manufacturing equipment validation.
• Experience developing and reviewing validation lifecycle documentation, including URS, IQ, OQ, PQ, Risk Assessments, and Validation Reports.
• Experience working collaboratively with Quality Assurance (QA), Manufacturing, Engineering, and IT teams.
• Strong understanding of the CSV lifecycle, risk-based validation, and documentation best practices.
• Excellent technical writing, documentation, communication, and problem-solving skills.
• Ability to manage multiple validation activities while maintaining compliance with regulatory and quality requirements.