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Csv Validation Engineer Jobs in Texas (NOW HIRING)

Spruce Infotech

Validation Expert

Fort Worth, TX · On-site

Work with project management to build an integrated project plan inclusive of the required Computer System Validation (CSV) Lifecycle Deliverables, quality gates and summarization milestones.

Stark Pharma Solutions Inc

CQV Engineer

Austin, TX · On-site

CQV Engineer Location: Austin, TX Duration: Long Term Position Overview We are seeking an ... Familiarity with clean utilities, HVAC systems, computerized systems validation (CSV), cleaning ...

Life Science Logistics LLC

AI Engineer

Coppell, TX

... DOCX, or CSV files uploaded through Claude Desktop. * Build and maintain internal evaluation ... validation, hallucination mitigation. * Experience with adversarial prompt testing, red teaming ...

Life Science Logistics

AI Engineer

Coppell, TX · On-site

... DOCX, or CSV files uploaded through Claude Desktop. * Build and maintain internal evaluation ... validation, hallucination mitigation. * Experience with adversarial prompt testing, red teaming ...

Lancer Hospitality

Integration Engineer

Houston, TX · On-site

$90 - $110/hr

Implement data transformation, validation, and error‑handling logic within integration workflows ... Experience working with JSON, XML, CSV, and other common data exchange formats. * Familiarity with ...

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Csv Validation Engineer information

What are the key skills and qualifications needed to thrive as a CSV validation engineer, and why are they important?

To thrive as a CSV (Computer System Validation) Validation Engineer, you need expertise in validation methodologies, regulatory compliance (such as FDA 21 CFR Part 11), and a background in life sciences or engineering. Familiarity with validation tools, documentation systems, and quality management software is typically required, along with knowledge of industry standards like GAMP 5. Strong attention to detail, analytical thinking, and effective communication skills set outstanding candidates apart. These competencies ensure validated systems meet regulatory requirements, maintain data integrity, and support safe, compliant operations in regulated environments.

What is a CSV validation engineer?

CSV Validation Engineers are professionals responsible for ensuring that computerized systems used in regulated industries, such as pharmaceuticals or biotechnology, comply with industry standards and regulations. CSV stands for Computer System Validation, which involves testing and documenting that systems function as intended and meet regulatory requirements for data integrity and security. These engineers typically create validation protocols, perform risk assessments, and support audits. Their work is crucial to ensure that electronic records and processes are reliable, traceable, and meet legal and industry guidelines.

What are some common challenges faced by a CSV validation engineer when working with cross-functional teams?

As a CSV Validation Engineer, one common challenge is ensuring clear communication and understanding between IT, QA, and business process teams regarding regulatory requirements and validation protocols. Misalignment on validation deliverables or timelines can occur, especially when teams have differing priorities or levels of familiarity with compliance frameworks. Proactively facilitating discussions, clarifying documentation, and providing training on Computer System Validation standards can help bridge gaps and keep projects on track.

What is the difference between Csv Validation Engineer vs Data Quality Analyst?

AspectCsv Validation EngineerData Quality Analyst
Required CredentialsBachelor's in Computer Science, Data Management, or related field; familiarity with data validation toolsBachelor's in Data Science, Statistics, or related; certifications like CDMP are common
Work EnvironmentData teams, software development, quality assuranceData analysis, reporting, data governance teams
Industry UsageTech, finance, healthcare, where data validation is criticalBusiness intelligence, analytics, data management sectors

The Csv Validation Engineer primarily focuses on validating and ensuring the accuracy of CSV data files through automated tools and scripts. In contrast, the Data Quality Analyst evaluates overall data quality, identifies issues, and implements data governance practices. Both roles require strong analytical skills and familiarity with data management, but their core responsibilities differ in scope and focus.

What are popular job titles related to Csv Validation Engineer jobs in Texas? For Csv Validation Engineer jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Csv Validation Engineer jobs in Texas look for? The top searched job categories for Csv Validation Engineer jobs in Texas are:
What cities in Texas are hiring for Csv Validation Engineer jobs? Cities in Texas with the most Csv Validation Engineer job openings:
Csv Validation Engineer jobs near you
Infographic showing various Csv Validation Engineer job openings in Texas as of August 2026, with employment types broken down into 92% Full Time, 3% Part Time, and 5% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution.

Validation (CQV) Engineer

BioPharma Consulting JAD Group

College Station, TX • On-site

Contractor

Life

Posted 8 days ago

Job description

The Validation Engineer is responsible for providing scientific and technical support for product launches, technology transfers, and new technology introductions at the FDBT site. This role executes key validation lifecycle activities-including Cycle Development (CD), Commissioning & Qualification (CQ), Performance Qualification (PQ), and Periodic Reviews (PR)-while collaborating closely with crossfunctional teams across the site and occasionally with network partners. Emphasis is placed on rightfirsttime execution, compliance, and continuous improvement.

Key Requirements

  • Onsite role; remote work is not permitted.
  • Experience creating full validation lifecycle documentation:
    • URS, FRS, DS, engineering specifications
    • Validation protocols (VPP, IQ, OQ, PQ)
    • System Impact Assessments, Requirements Traceability Matrix, Final Reports
  • Strong understanding of validation processes and regulatory requirements.
  • Ability to independently troubleshoot, resolve, and communicate technical issues.
  • Proven experience leading crossfunctional teams and coordinating complex projects.
  • Ability to develop and manage detailed project plans and timelines for IQ/OQ/PQ/RQP execution.
  • Working knowledge of Computerized Systems Validation (CSV).
  • Support implementation of new process technologies aligned with business and regulatory needs.
  • Ownership of vendorperformed validation activities, including:
    • Review and approval of vendor protocols
    • Issue resolution
    • Validation deviation reporting
    • Summary report generation
  • Coordinate and execute tactical validation activities:
    • Sample collection
    • Data retrieval
    • Documentation completion per protocol requirements
  • Excellent technical writing skills for SOP creation and updates.
  • Proficiency in Microsoft Word, Excel, and PowerPoint.
  • Ability to work independently, multitask, and support multiple projects simultaneously.
  • Provide guidance and support to junior team members.
  • Must be available to work as needed, including holidays and weekends.

Areas of Expertise

  • Kneat electronic validation documentation
  • Data loggers (pre/post calibration procedures)
  • Temperature mapping: cold rooms, freezers, refrigerators, incubators
  • Laboratory equipment (e.g., Mass Photometer)
  • Autoclaves & cycle development
  • EMPQs
  • Biowelders
  • Culture chemistry analyzers
  • Smoke studies
  • Fillers
  • VHP decontamination & cycle development
  • Bioquell Qube
  • Mixers, tanks, VCells
  • AKTA systems
  • Filter integrity testers
  • Pumps
  • Centrifuges
  • Downflow hoods
  • Weight scales
  • SME Water Systems (WFI, RODI)
  • Clean gas utilities
  • Facilities systems

Requirements

Education Requirements

  • Bachelor's degree in Engineering or Science (minimum).
  • 7+ years of validation experience in the life sciences industry.

Benefits

  • Administrative shift
  • 1-year contract with possible extension

Apply