CSV Engineer

Katalyst Talent Agency
Bloomfield, IN, United States
9 days ago
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Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Experience level
Expert
Experience required
7 years minimum
Working hours
Regular working hours

Tech stack

Audit Trail Data Integrity Requirements Traceability System Testing Iq/oq/pq Information Technology GXP

Job description

The CSV (Computer System Validation) Engineer will be responsible for ensuring that computerized systems used in a pharmaceutical/GMP-regulated environment are validated and compliant with regulatory standards, including 21 CFR Part 11. The role requires strong expertise in GAMP 5 methodology, validation lifecycle processes, and experience with automation and control systems. This is an onsite position based in Bloomfield, Indiana. Roles & Responsibilities:

  • Execute and manage computer system validation (CSV) activities in compliance with GAMP 5 and GMP regulations
  • Develop and review validation documentation including Validation Plans, URS (User Requirement Specifications), FS (Functional Specifications), DS (Design Specifications), and protocols (IQ/OQ/PQ)
  • Perform and oversee execution of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ)
  • Ensure compliance with 21 CFR Part 11 requirements, including electronic records, audit trails, and data integrity
  • Work with automation and control systems such as DeltaV, PI Historian, Rockwell PLC, HMI, or similar platforms
  • Apply risk-based validation approaches and V-model lifecycle principles
  • Maintain and manage validation documentation such as RTMs (Requirement Traceability Matrices), validation summary reports, and SOPs
  • Collaborate with cross-functional teams including Automation, Quality Assurance, and IT
  • Support internal and external audits by providing validation documentation and compliance evidence

Requirements

  • Bachelor’s degree in Engineering, Computer Science, Life Sciences, or a related field
  • Minimum of 7+ years of experience in Computer System Validation within a pharmaceutical or GMP-regulated environment
  • Strong knowledge of GAMP 5 methodology, V-model lifecycle, and risk-based validation approaches
  • Hands-on experience with automation and control systems (e.g., DeltaV, PI Historian, Rockwell PLC, HMI)
  • Proven experience supporting 21 CFR Part 11 compliance and data integrity requirements
  • Excellent documentation, communication, and stakeholder management skills

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