> Markdown version of [/jobs/ext/3321918-csv-consultant](https://www.wearedevelopers.com/jobs/ext/3321918-csv-consultant). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # CSV Consultant - **Company:** Katalyst Talent Agency - **Location:** Rapid City, SD, United States - **Contract:** Permanent contract - **Skills:** Data Analysis, Bioinformatics, Computational Biology, Data Integrity, Python (Programming Language), System Testing, Automated Data Processing (ADP), Iq/oq/pq, GXP - **Published:** September 7, 2026 - **Apply:** https://www.indeed.com/viewjob?jk=d9b735ac62116369 ## About the Role * Computer System Validation (CSV) in Pharmaceutical/Biotechnology environments. * Validation of laboratory or scientific software in GxP environments. * Bioinformatics, Genomics, NGS, or Computational Biology workflows. * Scientific algorithms and Python/R-based data analysis pipelines. * Strong knowledge of GAMP 5, 21 CFR Part 11, and data integrity principles. * Experience collaborating with Quality, IT, Bioinformatics, and Laboratory teams. ## Description We're looking for an experienced Computer System Validation (CSV) Consultant to support a leading biotech client in validating bioinformatics software, scientific algorithms, and data analysis platforms within a GMP-regulated environment. Roles & Responsibilities: * Validate bioinformatics software and data analysis systems. * Develop and execute Validation Plans, Risk Assessments, URS, IQ/OQ/PQ protocols, and Validation Summary Reports. * Validate scientific algorithms and automated data processing workflows. * Support laboratory software, genomic analysis platforms, and cloud-based application implementations/upgrades. * Perform impact assessments and support change control activities. * Ensure compliance with GAMP 5, 21 CFR Part 11, and data integrity requirements.