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Computer System Validation Csv Jobs in Indiana (NOW HIRING)

PM Group

CSV Engineer I

Indianapolis, IN · On-site

$68K - $88K/yr

We are looking for a CSV Computer System Validation Engineer who will support protocol execution for laboratory computer systems within a GxP manufacturing site. This individual should have a ...

PM Group

CSV Engineer I

Indianapolis, IN · On-site

$68K - $88K/yr

We are looking for a CSV Computer System Validation Engineer who will support protocol execution for laboratory computer systems within a GxP manufacturing site. This individual should have a ...

PM Group

CSV Engineer III

Indianapolis, IN · On-site

$68K - $88K/yr

This is a senior-level Computer System Validation (CSV) role for an experienced validation professional who will focus on executing CSV protocols for laboratory computerized systems in a GxP ...

PM Group

CSV Engineer III

Indianapolis, IN · On-site

$68K - $88K/yr

This is a senior-level Computer System Validation (CSV) role for an experienced validation professional who will focus on executing CSV protocols for laboratory computerized systems in a GxP ...

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Computer System Validation Csv information

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How much do computer system validation csv jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for computer system validation csv in Indiana is $49.29, according to ZipRecruiter salary data. Most workers in this role earn between $37.07 and $61.30 per hour, depending on experience, location, and employer.

What is a computer system validation CSV?

A Computer System Validation (CSV) job involves ensuring that computerized systems used in regulated industries, such as pharmaceuticals and medical devices, comply with industry standards and regulatory requirements (e.g., FDA 21 CFR Part 11, GxP). CSV professionals develop validation protocols, conduct testing, and document system performance to ensure data integrity, reliability, and compliance. Their role is critical in maintaining system quality and avoiding regulatory risks.

What are the key skills and qualifications needed to thrive in computer system validation CSV?

To thrive as a Computer System Validation (CSV) professional, you need a solid understanding of computer science, regulatory compliance (such as FDA 21 CFR Part 11), and validation methodology, often supported by a degree in a scientific or technical field. Familiarity with documentation tools, validation protocols, and quality management systems, as well as certifications like PMP or Six Sigma, is highly beneficial. Strong attention to detail, problem-solving abilities, and effective communication skills enable effective cross-functional collaboration. Mastering these skills ensures accurate validation processes, regulatory compliance, and smooth project execution in highly regulated environments.

What are some typical challenges faced by computer system validation CSV professionals and how are they addressed?

Computer System Validation (CSV) professionals often encounter challenges such as keeping up with evolving regulations, managing complex documentation requirements, and ensuring robust communication between IT, quality assurance, and business teams. Navigating system upgrades while maintaining compliance with strict regulatory standards requires careful planning and thorough risk assessment. Successful candidates address these challenges by staying current with industry guidance, utilizing validation templates and checklists, and fostering strong teamwork across various departments. Building collaborative relationships and maintaining meticulous records help ensure both audit readiness and smooth project completion.

Is computer system validation a good field?

Computer System Validation (CSV) is a specialized field within regulated industries like pharmaceuticals and biotech, focusing on ensuring software and systems meet compliance standards such as GxP. It offers opportunities for professionals with skills in quality assurance, validation protocols, and regulatory requirements, often requiring certifications like GAMP or 21 CFR Part 11 knowledge. The field provides stable employment with growth potential, especially as compliance regulations become more stringent.

What are the most commonly searched types of Computer System Validation Csv jobs in Indiana?

The most popular types of Computer System Validation Csv jobs in Indiana are:

What are popular job titles related to Computer System Validation Csv jobs in Indiana?

For Computer System Validation Csv jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Computer System Validation Csv jobs in Indiana look for?

The top searched job categories for Computer System Validation Csv jobs in Indiana are:

Computer System Validation Csv jobs near you
Infographic showing various Computer System Validation Csv job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $102,528 per year, or $49.3 per hour.

Computer System Validation Engineer

Stark Pharma Solutions Inc

Indianapolis, IN • On-site

Contractor

Re-posted 24 days ago

Job description

Job Title: Validation Engineer

Location: Indianapolis / Bloomington, IN (100% Onsite)

Duration: Long term Contract

Interview Mode: Onsite (Local candidates preferred)

Job Summary:

We are seeking a Validation Engineer with strong experience in Computer Systems Validation (CSV), equipment qualification, and GMP-regulated environments. The ideal candidate will support validation activities, documentation migration, and equipment qualification to ensure compliance with regulatory standards.

Key Responsibilities

  • Lead migration of legacy validation documents into the Kneat digital platform, ensuring accuracy and compliance
  • Perform equipment qualification for lab instruments (pH meters, thermal mixers, peristaltic pumps, nutating mixers, etc.)
  • Execute temperature mapping studies, including work with Ellab systems or similar equipment
  • Support Computer Systems Validation (CSV) activities and documentation
  • Assist Process Engineering teams to ensure project timelines and milestones are met
  • Ensure all validation activities comply with GMP and regulatory requirements
  • Maintain clear, accurate, and compliant documentation

Required Qualifications:

  • Bachelor’s degree in Engineering, Science, or related field
  • 6+ years of experience in Computer Systems Validation (CSV)
  • 4+ years of experience in pharmaceutical manufacturing environment
  • Hands-on experience with equipment qualification and validation
  • Strong knowledge of CSV principles and regulatory compliance
  • Experience working in onsite, fast-paced environments