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Computer Validation Jobs in Indiana (NOW HIRING)

CACI International, Inc.

Computer Engineer

Crane, IN · On-site

$111K - $131K/yr

Computer Engineer Job Category: Engineering Time Type: Full time Minimum Clearance Required to ... Validate hardware integration performance using approved industry and site-specific construction ...

Amatriot Group, LLC

Computer Engineer

Crane, IN · On-site

$120 - $150/hr

Validate hardware integration performance using approved industry and site-specific construction ... Proficiency in CAD software and knowledge of simulation and analysis tools * Experience with ...

Amatriot Group, LLC

Computer Engineer

Crane, IN

$120K - $150K/yr

The Computer Engineer will conduct research, develop engineering solutions, and collaborate with ... Validate hardware integration performance using approved industry standards, site-specific ...

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Showing results 21-40

All JobsComputer Validation JobsComputer Validation Jobs in Indiana

Computer Validation information

See Indiana salary details

$10

$51

$81

How much do computer validation jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for computer validation in Indiana is $51.69, according to ZipRecruiter salary data. Most workers in this role earn between $39.81 and $61.30 per hour, depending on experience, location, and employer.

What is the difference between Computer Validation vs Quality Assurance Specialist?

AspectComputer ValidationQuality Assurance Specialist
Required CredentialsGxP, 21 CFR Part 11, validation certificationsISO standards, QA certifications, GxP knowledge
Work EnvironmentPharmaceutical, biotech, regulated industriesManufacturing, healthcare, regulated industries
Employer & Industry UsageRegulated industries requiring validated systemsEnsuring quality compliance across processes

Computer Validation focuses on verifying that computer systems meet regulatory requirements and function correctly, primarily in regulated industries. Quality Assurance Specialists oversee overall quality processes, ensuring compliance and standards across various operations. While both roles require knowledge of GxP and industry regulations, Computer Validation is more technical and system-specific, whereas QA Specialists have a broader scope in quality management.

Is computer validation a good field?

Computer validation is a specialized field within quality assurance and regulatory compliance, focusing on ensuring that computerized systems meet industry standards such as 21 CFR Part 11. It often requires knowledge of validation protocols, testing, and documentation, and can offer stable employment opportunities in regulated industries like pharmaceuticals and biotech. The field values certifications and technical skills, making it suitable for professionals interested in compliance, quality systems, and technology validation.

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

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

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

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

What cities in Indiana are hiring for Computer Validation jobs?

Cities in Indiana with the most Computer Validation job openings:

Computer Validation jobs near you
Infographic showing various Computer Validation job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, 2% Contract, and 1% Nights. Highlights an 78% Physical, 2% Hybrid, and 20% Remote job distribution, with an average salary of $107,510 per year, or $51.7 per hour.

CSV / Validation Specialist - BMS

Spruce Infotech

Indianapolis, IN • On-site

Contractor

Re-posted 20 days ago

Job description

  • Lead the BMS validation lifecycle across all 8 LMF buildings, from URS authoring through Validation Summary Report and closeout.
  • Author and obtain approval for User Requirement Specifications (URS) for the Metasys BMS platform.
  • Engage JCI on Software Requirement Specifications (SRS) review and acceptance.
  • Develop and execute Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols.
  • Risk based approach adhering to Lilly Quality procedures.
  • Generate and maintain requirements traceability matrices (RTMs) linking requirements through design, testing, and acceptance.
  • Author Validation Summary Reports (VSR) documenting validation outcomes, deviations, and acceptance rationale.
  • Perform 21 CFR Part 11 gap assessments for electronic records, electronic signatures, and audit trail compliance across Metasys and AVEVA PI.
  • Coordinate with the Integration Engineer on alarm management validation (ISA 18.2) and OT cybersecurity validation (ISA/IEC 62443).
  • Validate OPC/UA integration between Metasys, AVEVA PI, and DeltaV QBMS.
  • Draft commissioning protocols and support system acceptance testing.
  • Draft and maintain SOPs related to BMS operations, operator training, and preventive maintenance.
  • Enroll systems into the periodic review program for ongoing validated-state maintenance.
  • Support audit readiness by ensuring validation documentation is inspection-ready and aligned with FDA, EMA, and Lilly corporate quality standards.
  • Provide support for data integrity assessments across BMS and historian systems.
  • Assist with commissioning and qualification (C&Q) activities for new BMS equipment.
  • Support remediation of validation findings from internal audits or regulatory inspections.
  • Advise on validation strategy for future BMS system upgrades and expansions.
  • Demonstrated experience in computer systems validation (CSV) for building management or automation and control systems in a pharmaceutical/GMP-regulated environment.
  • Strong knowledge of GAMP 5 methodology, V-model lifecycle, and risk-based validation approaches.
  • Experience with 21 CFR Part 11 compliance, including assessment of electronic records, electronic signatures, and audit trail requirements.
  • Proficiency in developing validation deliverables: VP, URS, FS, DS, IQ/OQ/PQ protocols, RTMs, and VSRs.
  • Experience with BMS, DCS, PLC/HMI, or historian systems in a manufacturing environment.
  • Strong understanding of FDA and EMA regulatory expectations for computerized system validation.
  • Direct experience validating JCI Metasys, Honeywell, Siemens, or similar BMS platforms.
  • Experience with AVEVA PI Historian, DeltaV, or OPC/UA integration validation.
  • Familiarity with ISA 18.2 alarm management and ISA/IEC 62443 cybersecurity standards.
  • Familiarity with data integrity principles (ALCOA+) and data governance frameworks.
  • Experience with Kneat, ValGenesis, or similar electronic validation management systems.

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