Bioinformatics CSV Specialist — GMP/GxP Validation Expert

Creative Solutions Services, LLC

Philadelphia (Philadelphia County)

On-site

USD 120,000 - 160,000

Full time

11 days ago
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Job summary

Creative Solutions Services, LLC is seeking 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.

You will develop and execute Validation Plans, Risk Assessments, URS, IQ/OQ/PQ, and Validation Summary Reports, validate automated data workflows, and ensure compliance with GAMP 5 and FDA data integrity standards.

Qualifications

  • Experience validating CSV in GMP-regulated environments.
  • Experience validating laboratory or scientific software in GxP environments.
  • Knowledge of GAMP 5 and data integrity principles.

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 applications.
  • Perform impact assessments and support change control activities.
  • Ensure compliance with GAMP 5, 21 CFR Part 11, and data integrity requirements.

Skills

CSV in Pharma/Biotech
GxP environments
Bioinformatics workflows
Python/R data analysis
GAMP 5/21 CFR Part 11
Quality/IT collaboration

Tools

IQ/OQ/PQ execution
Validation Plans/Reports

Job description

Creative Solutions Services, LLC is seeking 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.

You will develop and execute Validation Plans, Risk Assessments, URS, IQ/OQ/PQ, and Validation Summary Reports, validate automated data workflows, and ensure compliance with GAMP 5 and FDA data integrity standards.

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