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Csv Engineer Jobs in Texas (NOW HIRING)

Stevens Transport

IT Senior Developer

Dallas, TX · On-site

$54 - $71.25/hr

Stevens Transport is seeking an IT Senior Developer responsible for the ongoing development and ... CSV reports • Integrated File Systems • Project management • Demonstrated ability to ...

Fynbosys Inc

Azure Data Engineer

San Antonio, TX · On-site

$104K - $125K/yr

ob Summary We are seeking an experienced Azure Data Engineer to design, develop, and maintain ... Parquet, Delta Lake, JSON, CSV * Methodologies: Agile, Scrum

Stevenstransport

IT Senior Developer

Dallas, TX · On-site

$54 - $71.25/hr

Working closely with other developers under the guidance of our IT Director, the purpose of this ... XLS/CSV reports * Integrated File Systems * Project management * Demonstrated ability to ...

PamTen Inc

Mulesoft Developer

Plano, TX · On-site

Familiarity with XML, JSON, CSV, and other relevant data formats. • Java: Strong understanding of ... MuleSoft Certified Developer Company : PAMTEN is established in the year 2007 as a technology ...

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$33K

$91.2K

$126.1K

How much do csv engineer jobs pay per year?

As of Aug 16, 2026, the average yearly pay for csv engineer in Texas is $91,188.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,600.00 and $106,900.00 per year, depending on experience, location, and employer.

What is the salary of CSV engineer?

The salary of a CSV engineer typically ranges from $70,000 to $120,000 annually, depending on experience, location, and industry. Skilled professionals with expertise in data processing, scripting, and database management tend to earn higher salaries. Certifications in data engineering or related tools can also influence compensation.

How much do CSV engineers make?

CSV engineers typically earn between $70,000 and $120,000 annually, depending on experience, location, and industry. Skilled professionals with expertise in data processing, scripting, and database management tend to command higher salaries.

What is a CSV engineer?

A CSV (Computer System Validation) Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, comply with regulatory requirements. They develop validation protocols, perform testing, document results, and ensure adherence to industry standards like FDA 21 CFR Part 11 and GAMP 5. Their goal is to confirm that software and hardware systems function correctly, maintain data integrity, and meet compliance requirements.

What does a CSV engineer do?

A CSV engineer specializes in designing, developing, and maintaining systems that process and manage data stored in CSV (comma-separated values) format. They often work with data pipelines, scripting languages like Python or SQL, and data validation tools to ensure accurate data handling and integration across applications.

What are the common challenges faced by a CSV engineer in the pharmaceutical or medical device industry?

CSV Engineers in the pharmaceutical or medical device industry often face the challenge of keeping up with evolving regulatory requirements and ensuring all computerized systems remain compliant throughout their lifecycle. Managing comprehensive documentation, coordinating with multiple departments, and troubleshooting complex system changes can add to the workload. Successful CSV Engineers are proactive about staying informed of regulatory updates, are highly organized, and collaborate closely with Quality Assurance, IT, and operations teams. This dynamic environment offers the opportunity to learn continuously, develop expertise in validation best practices, and advance into leadership or specialized quality roles.

What are the key skills and qualifications needed to thrive as a CSV engineer?

To thrive as a CSV Engineer (Computer System Validation Engineer), you need a solid understanding of validation principles, regulatory compliance (such as FDA 21 CFR Part 11), and a relevant degree in life sciences, engineering, or information technology. Familiarity with validation lifecycle documentation, risk assessment tools, and industry-standard systems like SAP, LIMS, and TrackWise is highly valued, as are certifications such as GAMP or Six Sigma. Strong attention to detail, analytical thinking, and excellent communication skills help CSV Engineers collaborate efficiently with cross-functional teams and ensure thorough documentation. These skills are crucial to guarantee that computerized systems in regulated industries meet compliance requirements, supporting product quality and patient safety.

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What job categories do people searching Csv Engineer jobs in Texas look for?

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Csv Engineer jobs near you
Infographic showing various Csv Engineer job openings in Texas as of August 2026, with employment types broken down into 60% Full Time, and 40% Contract. Highlights an 100% In-person job distribution, with an average salary of $91,188 per year, or $43.8 per hour.

Senior CSV Engineer

Katalyst Healthcares and Lifesciences

Austin, TX • On-site

$103K - $142K/yr

Other

Posted 2 days ago

New

Job description

Job Description:
The Senior Computer System Validation (CSV) Engineer is responsible for leading validation activities for computerized systems used in regulated environments such as pharmaceutical, biotechnology, or medical device manufacturing. This role ensures that systems including LIMS, ERP, MES, and laboratory applications are validated in compliance with FDA, EU, and global regulatory requirements. The Senior CSV Engineer will act as a subject matter expert (SME), providing guidance on validation strategy, risk-based approaches, and regulatory compliance across the system lifecycle.
Responsibilities:
  • Lead and execute computer system validation (CSV) activities for GxP-regulated systems.
  • Develop and review validation deliverables including validation plans, URS, FS, DS, risk assessments, IQ/OQ/PQ protocols, and summary reports.
  • Ensure compliance with FDA 21 CFR Part 11, EU Annex 11, GAMP 5, and GxP regulations.
  • Define and implement risk-based validation strategies for computerized systems.
  • Oversee validation of systems such as LIMS, ELN, MES, ERP, CDS, and laboratory systems.
  • Support system implementations, upgrades, and decommissioning activities from a validation perspective.
  • Collaborate with IT, QA, Engineering, and business stakeholders to ensure compliant system deployment.
  • Lead change control assessments and determine validation impact of system changes.
  • Ensure data integrity (ALCOA+) compliance across validated systems.
  • Support audits and regulatory inspections by providing validation documentation and system justification.
  • Mentor and guide junior CSV engineers and validation team members.
  • Drive continuous improvement of validation processes, templates, and standards.
  • Review vendor documentation and ensure systems meet regulatory expectations prior to deployment.
Requirements:
  • Bachelor's degree in Engineering, Computer Science, Life Sciences, or related field.
  • 5-10+ years of experience in Computer System Validation (CSV) or validation engineering.
  • Strong experience in GxP-regulated pharmaceutical, biotech, or medical device environments.
  • Hands-on experience with validation of LIMS, MES, ERP, or laboratory systems.
  • Strong knowledge of 21 CFR Part 11, EU Annex 11, and GAMP 5 guidelines.
  • Experience authoring and executing IQ/OQ/PQ protocols and validation documentation.
  • Strong understanding of risk-based validation and data integrity principles.
  • Experience supporting regulatory audits and inspections.
Preferred Skills:
  • Experience with systems such as LabWare, SAP, Oracle, Veeva, TrackWise, Empower.
  • Knowledge of cloud-based validation and SaaS systems.
  • Experience in data integrity remediation projects.
  • Strong technical writing and documentation skills.
  • bility to lead cross-functional validation projects.
Key Competencies:
  • Strong leadership and SME-level expertise in CSV.
  • Excellent analytical and risk assessment skills.
  • Strong communication and stakeholder management.
  • bility to manage multiple validation projects simultaneously.
  • High attention to detail and regulatory compliance mindset.

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