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Computer System Validation
Programming.com
Mexico, USA, United States of America
Not Disclosed
4 - 8 Years
Full Time
Views:92
Applicants:1
Posted on 15 Dec, 2025
Hybrid
Job Description | Responsibilities
- 4+ years of hands-on CSV experience in pharma, biotech, or CRO
- Deep understanding of GCP/GLP processes and regulatory expectations
- Proven track record preparing systems and documentation for regulatory audits
- Strong documentation, communication, and problem-solving skills
Overview
- Industry - IT - Consulting Services / Advisory Services
- Functional Area - Other
- Job Role - Other
- Employment type - Full Time
- Work Mode - Hybrid
Qualifications
- Any Graduate - Any Specialization
- Any Post Graduate - Any Specialization
- Any Doctorate - Any Specialization
Job Related Keywords
Computer System Validation
Computer System
Computer system validation
