CSV Engineer
Job in
Bloomfield, Greene County, Indiana, 47424, USA
Listed on 2026-07-16
Listing for:
Creative Solutions Services, LLC
Full Time
position Listed on 2026-07-16
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering
Job Description & How to Apply Below
Job Summary:
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
- 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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