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Csv Engineer Jobs (NOW HIRING)

Job Title: CSV Engineer I Location: Social Circle, Georgia, USA Duration: Longterm Job Summary The CSV Engineer supports validation activities for computerized systems used in pharmaceutical ...

CSV Engineer

Mount Horeb, WI ยท On-site

$120K - $135K/yr

The CSV Engineer will author validation deliverables--including protocols, reports, and SOPs--ensuring compliance with FDA, EMA, and global regulatory expectations. Key Responsibilities: * Develop ...

... CSV Engineer โ€ข Ensuring compliance with validation and regulatory standards Qualifications : Required : โ€ข Strong CSV (Computer System Validation) experience โ€ข Hands-on experience with Veeva ...

CSV Engineer

Costa Mesa, CA ยท On-site

$55 - $60/hr

CSV Engineer Costa Mesa, CA or Seattle, WA(On-site) Visa: USC, GC & H4 EAD Key Responsibilities: * Develop and maintain Design Specifications (DS) for computerized and automated systems. * Author and ...

CSV Engineer III

Indianapolis, IN ยท On-site

$68K - $88K/yr

Overview The CSV Engineer III position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team at a site near Indianapolis, IN . Outsourced Technical ...

New

CSV Engineer I

Indianapolis, IN ยท On-site

$68K - $88K/yr

Overview The CSV Engineer I position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team at a site near Indianapolis, IN . Outsourced Technical ...

New

CSV Engineer III

Indianapolis, IN ยท On-site

$68K - $88K/yr

Overview The CSV Engineer III position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team at a site near Indianapolis, IN . Outsourced Technical ...

New

Katalyst CRO is a company focused on providing services in the life sciences sector, and they are seeking an IT CSV Validation Engineer. This role is responsible for authoring and executing ...

CSV Engineer I

Indianapolis, IN ยท On-site

$68K - $88K/yr

Overview The CSV Engineer I position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team at a site near Indianapolis, IN . Outsourced Technical ...

New

2 days ago Be among the first 25 applicants Direct message the job poster from Staftonic LLC Experienced CSV Engineer with 6-7 years in GxP pharma environments, skilled in validating automation ...

CSV Engineer (6mo. Contract-to-Hire) Location: Baltimore, MD Company Join a premier global Contract Development and Manufacturing Organization (CDMO) that is rapidly expanding its state-of-the-art ...

The Senior Computer System Validation (CSV) Engineer is responsible for leading the validation of complex computerized systems, custom-developed applications, enterprise databases, data platforms ...

Katalyst CRO is seeking an IT CSV Validation Engineer responsible for authoring and executing validation test scripts to support regulated systems within a GxP life sciences environment. This role ...

CSV Engineer Location: Raritan, NJ(Hybrid) Mandatory - Validation experience with ERP applications / SAP / MES * Experience in validating ERP/SAP/ MES Manufacturing applications * 3+ years ...

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CSV Engineer information

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$36K

$99.4K

$137.5K

How much do csv engineer jobs pay per year?

As of Aug 8, 2026, the average yearly pay for csv engineer in the United States is $99,411.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,000.00 and $116,500.00 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.

More about CSV Engineer jobs
What cities are hiring for Csv Engineer jobs? Cities with the most Csv Engineer job openings:
What are the most commonly searched types of Csv Engineer jobs? The most popular types of Csv Engineer jobs are:
What states have the most Csv Engineer jobs? States with the most job openings for Csv Engineer jobs include:
Infographic showing various Csv Engineer job openings in the United States as of August 2026, with employment types broken down into 53% Full Time, and 47% Contract. Highlights an 100% In-person job distribution, with an average salary of $99,411 per year, or $47.8 per hour.

CSV Engineer

Intellectt INC

Social Circle, GA โ€ข On-site

Contractor

This job post hasย expired 1 day ago.ย Applications are no longer accepted.


Job description

Job Title: CSV Engineer I
Location: Social Circle, Georgia, USA
Duration: Longterm

Job Summary
The CSV Engineer supports validation activities for computerized systems used in pharmaceutical/biopharmaceutical manufacturing. The role focuses on ensuring systems, equipment, automation platforms, and validation documents meet GMP, quality, safety, and regulatory standards

Key Responsibilities

  • Support CSV and qualification activities for computerized systems, facilities, utilities, equipment, and automation systems used in production.
  • Prepare and execute validation documents such as commissioning, qualification, and validation protocols/reports.
  • Assist in equipment and system testing to confirm that systems meet quality, safety, reliability, and performance requirements.
  • Support change controls, deviations, investigations, and CAPAs by providing technical validation input and documentation support.
  • Work with SMEs and cross-functional teams to execute testing strategies and resolve validation-related issues.
  • Participate in risk and impact assessments to identify validation requirements and system risks.
  • Review and support SOPs and validation assessments to maintain compliance with GMP standards.
  • Support audits and regulatory inspections as part of the Engineering Validation team when required.

Skills Required

  • Bachelor’s degree in Engineering or related computerized systems field.
  • Basic knowledge of CSV, CQV, GMP, and validation lifecycle.
  • Understanding of pharma regulations/guidelines such as FDA, ICH, ISO, EU GMP, ISPE, PDA.
  • Knowledge of automation/control systems like DeltaV, Honeywell, Rockwell PLC, Siemens is a plus.
  • Good documentation, writing, and communication skills.
  • Basic knowledge of Microsoft Word, Excel, PowerPoint; MS Project/Visio is a plus.
  • Ability to work with change control, deviations, CAPA, SOPs, and validation protocols.
  • Experience  CSV/CQV or GMP-regulated environment preferred.                                                                                                                                                                                                                                                                                                                                                                     

    For more information, please reach out at 732-719-4936 or share your updated resume with padma.priya@intellectt.com.