CSV Consultant (Computer System Validation)
Automate your job search with Sonara.
Submit 10x as many applications with less effort than one manual application.1
Reclaim your time by letting our AI handle the grunt work of job searching.
We continuously scan millions of openings to find your top matches.
Overview
Job Description
Job Title: CSV Consultant (Computer Systems Validation)
Location: Redwood City, CA
Type: Contract
Job Summary
We are seeking an experienced CSV Consultant to support validation activities across multiple GxP-regulated systems within a pharmaceutical environment. This role will focus on computer systems validation, revalidation efforts, data migration activities, and documentation management for critical business and quality systems.
The ideal candidate will have strong experience with validated systems, change control processes, and regulatory compliance in GMP/GxP environments.
Key Responsibilities
- Lead and support validation activities for GxP-regulated systems including:
- SAS Studio
- Veeva Quality Docs
- CTMS
- TraceLink
- Argus
- Support system revalidation and data migration projects to ensure compliance and data integrity
- Develop, review, and execute validation documentation including:
- Validation Plans
- User Requirements Specifications (URS)
- Risk Assessments
- IQ/OQ/PQ protocols
- Traceability Matrices
- Summary Reports
- Create and support User Acceptance Testing (UAT) scripts and execution activities
- Manage change control documentation and support deviation resolution activities
- Ensure validation activities align with FDA, GAMP5, and GxP compliance requirements
- Collaborate with IT, Quality, Clinical, and Business stakeholders to support validated system implementations and updates
- Maintain accurate and compliant documentation throughout the system lifecycle
Required Qualifications
- Bachelor's degree in Computer Science, Engineering, Life Sciences, or related field
- 5+ years of experience in Computer Systems Validation (CSV) within pharmaceutical or biotech environments
- Hands-on experience validating GxP systems and supporting regulated system implementations
- Strong knowledge of FDA 21 CFR Part 11, GAMP5, and GxP requirements
- Experience with validation documentation, UAT execution, and change control processes
- Familiarity with systems such as SAS Studio, Veeva, CTMS, TraceLink, or Argus
- Strong analytical, documentation, and communication skills
Automate your job search with Sonara.
Submit 10x as many applications with less effort than one manual application.
