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# CSV Specialist

- **Company:** Katalyst Talent Agency
- **Location:** Santa Fe, NM, United States
- **Experience:** Experienced
- **Contract:** Permanent contract
- **Skills:** Software Applications, JIRA, Data Integrity, Document Management Systems, Laboratory Information Management Systems, SAP (Applications), Microsoft SharePoint, System Testing, Iq/oq/pq, Information Technology, Trackwise, Veeva, GXP, Servicenow
- **Published:** November 5, 2026
- **Apply:** https://www.thejobnetwork.com/job/cc0fed52-c486-41d6-a5a0-644afecd0bca/csv-specialist

## About the Role

* Bachelor's degree in engineering, Computer Science, Life Sciences, Pharmacy, Biotechnology, or related field.
 * 3 years of CSV experience in a regulated pharmaceutical, biotechnology, or medical device environment.
 * Knowledge of GAMP 5, FDA 21 CFR Part 11, GMP, and Data Integrity (ALCOA ) principles.
 * Experience with validation documentation and testing activities.
 * Familiarity with electronic quality management and document management systems.
 * Strong technical writing and communication skills., * Experience with CSA (Computer Software Assurance) methodologies.
 * Knowledge of systems such as:
 + TrackWise
 + Veeva
 + SAP
 + LIMS
 + MES
 + Empower
 + SharePoint
 + ServiceNow
 + Jira
 * Experience supporting regulatory audits and inspections.

## Description

We are seeking a CSV Specialist to support Computer System Validation (CSV) activities for GxP-regulated systems in the pharmaceutical, biotechnology, or medical device industry. The ideal candidate will be responsible for ensuring computerized systems are validated and compliant with regulatory requirements, company procedures, and industry standards.
Responsibilities:

 * Execute and support Computer System Validation (CSV) activities for GxP systems.
 * Develop, review, and maintain validation documentation, including:
 + Validation Plans
 + User Requirements Specifications (URS)
 + Functional Specifications (FS)
 + Risk Assessments
 + IQ/OQ/PQ Protocols
 + Validation Reports
 * Perform system impact assessments and risk-based validation activities.
 * Support testing activities, including protocol execution and defect tracking.
 * Ensure compliance with FDA 21 CFR Part 11, GAMP 5, GMP, and Data Integrity requirements.
 * Collaborate with Business, IT, QA, and Engineering teams throughout the system lifecycle.
 * Support change controls, deviations, CAPAs, and periodic reviews.
 * Maintain validation records within electronic document management systems.
 * Participate in internal audits and regulatory inspections.