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Csv Validation Engineer Jobs in Indiana (NOW HIRING)

EXOS

Senior CSV Validation Specialist

Indianapolis, IN · On-site

Our client is seeking a Senior CSV Validation Specialist dedicated to Building Management System ... The role supports the Site Automation Engineering organization and works closely with automation ...

CAI

Computer Systems Validation Engineer

Indianapolis, IN · On-site

$75K - $106K/yr

... CSV activities across various platforms including MES, DCS, SCADA, and batch systems Engage with ... validation compliance and delivery Qualifications and Experience Bachelor's degree (BS/BA) in ...

CAI

Computer Systems Validation Engineer

Indianapolis, IN · On-site

$75K - $106K/yr

... CSV activities across various platforms including MES, DCS, SCADA, and batch systems Engage with ... validation compliance and delivery Qualifications and Experience Bachelor's degree (BS/BA) in ...

CAI

Computer Systems Validation Engineer

Indianapolis, IN · On-site

$75K - $106K/yr

... CSV activities across various platforms including MES, DCS, SCADA, and batch systems Engage with ... validation compliance and delivery Qualifications and Experience Bachelor's degree (BS/BA) in ...

CAI

Computer Systems Validation Engineer

Indianapolis, IN · On-site

$75K - $106K/yr

... CSV activities across various platforms including MES, DCS, SCADA, and batch systems Engage with ... validation compliance and delivery Qualifications and Experience Bachelor's degree (BS/BA) in ...

Novartis

Site Equipment & CQV Lead

Indianapolis, IN

$124K - $186K/yr

Manage team of CQV/CSV and Equipment Engineers to maintain equipment reliability and ensuring ... validated state is maintained. Develops risk-based qualification approach and strategy (FMEA, Risk ...

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Csv Validation Engineer information

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$47

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How much do csv validation engineer jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for csv validation engineer in Indiana is $47.31, according to ZipRecruiter salary data. Most workers in this role earn between $35.38 and $57.12 per hour, depending on experience, location, and employer.

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 are Csv Validation Engineers?

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 Indiana? For Csv Validation Engineer jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Csv Validation Engineer jobs in Indiana look for? The top searched job categories for Csv Validation Engineer jobs in Indiana are:
Csv Validation Engineer jobs near you

Senior CSV Validation Specialist (Building Management Systems)

Stark Pharma Solutions Inc

Indianapolis, IN • On-site

Contractor

Posted 5 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Sr CSV Validation Specialist position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Position: Senior CSV Validation Specialist (Building Management Systems)

Location: Indianapolis, IN (100% Onsite)
Duration: Long Term
 

Job Overview

We are seeking an experienced Senior CSV Validation Specialist to support Building Management System (BMS) validation within a regulated pharmaceutical manufacturing environment. This role will lead the full Computer System Validation (CSV) lifecycle, ensuring compliance with FDA, EMA, and GAMP 5 requirements while partnering with Automation, IT, Engineering, and System Integrators.

Key Responsibilities

  • Lead end-to-end validation of Building Management Systems (BMS) from URS through Validation Summary Reports.
  • Author and execute validation documentation including URS, DQ, IQ, OQ, PQ, RTM, Validation Plans, and VSRs.
  • Review software requirements and collaborate with vendors, including Johnson Controls, on system validation activities.
  • Perform 21 CFR Part 11 assessments for electronic records, audit trails, and electronic signatures.
  • Validate integrations between Metasys, AVEVA PI, DeltaV, and OPC UA platforms.
  • Support commissioning, qualification, system acceptance testing, and periodic reviews.
  • Develop SOPs and maintain validation documentation in an inspection-ready state.
  • Support audit readiness, data integrity initiatives, remediation activities, and future system upgrades.
  • Collaborate with Automation, IT, Engineering, Quality, and Validation teams to ensure GMP compliance.

Required Qualifications

  • Strong experience in Computer System Validation (CSV) within pharmaceutical or GMP-regulated environments.
  • Hands-on experience validating Building Management Systems (BMS) or industrial control systems.
  • In-depth knowledge of GAMP 5, V-Model lifecycle, and risk-based validation methodologies.
  • Experience with 21 CFR Part 11 compliance and computerized system validation.
  • Proven experience authoring and executing CSV documentation, including URS, FS, DS, IQ, OQ, PQ, RTM, Validation Plans, and Validation Summary Reports.
  • Experience supporting BMS, DCS, PLC, HMI, or Historian systems.
  • Strong understanding of FDA and EMA regulatory requirements.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com