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# CSV Consultant

- **Company:** Katalyst Talent Agency
- **Location:** Flemington, NJ, United States
- **Contract:** Permanent contract
- **Skills:** Data Analysis, Bioinformatics, Computational Biology, Computer Engineering, Data Integrity, Python (Programming Language), System Testing, Automated Data Processing (ADP), Iq/oq/pq, Information Technology, GXP
- **Published:** October 17, 2026
- **Apply:** https://www.careerbuilder.com/job-details/csv-consultant-flemington-nj--6afa0635-50a4-4f5e-a45b-381a32f01ca3

## About the Role

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.

 * 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.
 * Bachelor's degree in Computer Science, Computer Engineering, Information Technology, Engineering, Life Sciences, Pharmacy, or a related field.

## 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.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.Bachelor's degree in Computer Science, Computer Engineering, Information Technology, Engineering, Life Sciences, Pharmacy, or a related field.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.