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# SAP Computer Systems Validation (CSV) Consultant

- **Company:** HEALTHCARE STAFFING INC
- **Location:** United States (Remote available)
- **Salary:** $72,800.0 - $83,200.0
- **Contract:** Temporary contract
- **Skills:** Data Integrity, SAP (Applications), Verification and Validation (Software), Iq/oq/pq, Test Scripts, Information Technology, GXP
- **Published:** August 5, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=098a8608eb4a2f40

## About the Role

* Proven experience in Computer Systems Validation (CSV) within regulated industries.
 * Strong technical writing skills, especially in protocol development and documentation.
 * In-depth understanding of quality assurance, quality control, and software validation.
 * Working knowledge of risk management principles and validation methodologies.
 * Familiarity with automation tools and electronic systems (preferred but not required).

## Description

We are seeking a CSV Consultant (Computer Systems Validation Expert) to support validation activities in regulated industries such as pharmaceuticals, medical devices, and biotechnology. The ideal candidate will be an experienced professional with a strong command of FDA 21 CFR Part 11, GAMP 5, and GxP requirements.

This role involves the full lifecycle of validation - from planning and writing detailed validation protocols to executing tests, documenting outcomes, and ensuring systems maintain data integrity and regulatory compliance., * Plan, write, and review validation protocols and related documentation for computer systems.

 * Draft and maintain test scripts, IQ/OQ/PQ protocols, and validation reports.
 * Conduct and document testing activities to verify systems function as intended and meet all regulatory and business requirements.
 * Ensure data integrity and adherence to FDA 21 CFR Part 11, GAMP 5, and GxP standards.
 * Collaborate with Quality Assurance, IT, and Regulatory Affairs teams to maintain compliance and support internal and external audits.
 * Develop and maintain validation documentation, including validation plans, specifications, standard operating procedures (SOPs), and risk assessments.
 * Support continuous improvement in validation and documentation processes.


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