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Computer System Validation Jobs in Indiana (NOW HIRING)

Senior Automation Engineer

Indianapolis, IN · On-site

$99.40K - $130.50K/yr

Support Computer System Validation activities, including Installation Qualification, Operational Qualification, and Performance Qualification. * Execute and review system verification and validation ...

Automation Project Lead

Indianapolis, IN

$90.80K - $119K/yr

... and computer system validation principles Strong knowledge of GMP's, regulatory requirements and computer system validation principles Excellent written and verbal communication skills for both ...

... computer system validation deliverables (alarm rationalization, system overview, source code reviews, testing, etc.) Secure vendor documents for skidded equipment to integrate with validation ...

Senior MES Engineer

Fishers, IN

$97.80K - $134.30K/yr

Provide technical support to Computer System Validation (CSV) activities, including MES qualification and data integrity assessments. Work closely with IT to implement OT solutions in an integrated ...

Support internal and external audits related to system validation and regulatory compliance ... Prolonged periods of sitting while working at a desk or computer. * Ability to occasionally lift up ...

Senior MES Engineer

Fishers, IN

$94.10K - $129.20K/yr

... to Computer System Validation (CSV) activities, including MES qualification and data integrity assessments. · Work closely with IT to implement OT solutions in an integrated and secure network.

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Computer System Validation information

See Indiana salary details

$10

$51

$81

How much do computer system validation jobs pay per hour?

As of May 30, 2026, the average hourly pay for computer system 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 a Computer System Validation job?

A Computer System Validation (CSV) job involves ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, meet compliance and regulatory requirements. CSV professionals develop and execute validation protocols to confirm that software, hardware, and processes function as intended and maintain data integrity. They work with quality assurance, IT, and regulatory teams to document compliance with standards like FDA 21 CFR Part 11 and GxP. This role is critical in maintaining system reliability, product quality, and patient safety.

What are the key skills and qualifications needed to thrive in the Computer System Validation position, and why are they important?

To excel in Computer System Validation, candidates typically need a background in computer science, engineering, or life sciences, with expertise in validating software and systems in regulated environments such as pharmaceuticals or medical devices. Familiarity with tools like validation documentation software, GAMP 5 guidelines, FDA 21 CFR Part 11 regulations, and potentially certifications like CSV Professional or Six Sigma is highly valued. Strong attention to detail, analytical thinking, and effective communication skills help professionals work collaboratively and document findings precisely. These abilities ensure compliance, data integrity, and the reliability of computerized systems critical to safety and quality.

What are some typical challenges faced in Computer System Validation roles?

Professionals in Computer System Validation often encounter challenges such as keeping up with evolving regulatory requirements, ensuring complete and accurate documentation, and coordinating with cross-functional teams to implement validation protocols. Balancing thoroughness with project deadlines can also be demanding, as every validation step must stand up to external audits. However, these challenges provide valuable experience, strengthen project management abilities, and emphasize teamwork—key attributes that support career advancement into validation leadership or quality assurance roles.
What are the most commonly searched types of Computer System Validation jobs in Indiana? The most popular types of Computer System Validation jobs in Indiana are:
What are popular job titles related to Computer System Validation jobs in Indiana? For Computer System Validation jobs in Indiana, the most frequently searched job titles are:
What cities in Indiana are hiring for Computer System Validation jobs? Cities in Indiana with the most Computer System Validation job openings:
Laboratory Systems Validation Specialist I

Laboratory Systems Validation Specialist I

Labcorp

Indianapolis, IN

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 21 days ago


Labcorp rating

6.6

Company rating: 6.6 out of 10

Based on 1,081 frontline employees who took The Breakroom Quiz

78th of 103 rated laboratories


Job description

Labcorp is seeking a Laboratory Systems Validation Specialist to join our team at Scicor Drive in Indianapolis, Indiana.

Work Schedule

Monday through Friday, day shift

Job Responsibilities

Technical & Operational Support

  • Operate and support laboratory instruments, interfaces, LIS/LIMS, and middleware platforms (e.g., Data Innovations Instrument Manager, Siemens CentraLink).
  • Lead and provide guidance during system validations for instruments, middleware, and other lab systems.
  • Support change control processes for laboratory systems.
  • Collaborate with SMEs to define expected system behaviors and translate them into clear technical requirements, including data workflow considerations across systems.
  • Provide technical consultation to internal and external clients.

Leadership & Project Management

  • Gather and document system requirements using established methodologies.
  • Create and maintain validation documentation; experience in GxP and CAP/CLIA environments preferred. Knowledge of SDLC/GAMP is a plus.
  • Lead testing activities for laboratory workflows, physical automation, and instrument middleware platforms.
  • Oversee requirements gathering for middleware interface development.
  • Coordinate with project managers and resource owners to support system testing.
  • Ensure timely delivery of services and maintain strong client relationships.
  • Drive client satisfaction and identify opportunities for additional business.

Performance Monitoring & Quality

  • Monitor system testing progress and performance metrics; identify and escalate issues when needed.
  • Review and prepare test results for QA to ensure complete, compliant test packages.
  • Balance operational support duties with ongoing project responsibilities.
  • Ensure adequate resource allocation to meet performance and quality standards.
  • Maintain regulatory compliance.
  • Collaborate with other sites and cross-functional teams.

General Responsibilities

  • Perform qualification specialist duties as needed.
  • Coordinate review, approval, and archiving of validation documentation.
  • Provide written and verbal updates to project managers and leadership.
  • Complete all HR- and training-related requirements; maintain an up-to-date training file.
  • Submit monthly status reports.
  • Support a culture of continuous improvement, quality, and productivity.

Minimum Qualifications

  • 3 or more years' experience in a Laboratory System Analyst or Laboratory System Validations role.
  • Bachelor of Science (BS) in Clinical Laboratory Science, Biology, Chemistry, Public Health, Microbiology, Computer, Technology, Animal Science, and/or Medical Technology

Preferred Qualifications

  • 1 or more years experience of knowledge of lab workflow and processes
  • 1 or more years experience in laboratory software testing such as Navify, FCS Express, Infinicyte
  • 1 or more years of experience or supporting client audits by providing an overview of the system validation documentation

Additional Job Standards

  • Experience in IT/Computer validation (to leverage important inputs on how to handle the workflow, howto avoiddata integrity problems,evaluate upfront solutions with less validation effort and capture any event possibility required bya system when setting complex rules)
  • Experience in requirements gathering, documentation in a regulatory environment
  • Strong knowledge of 21 CFR Part 11 requirements and CAP/CLIA regulations
  • Background in information systems, data analysis, workflow analysis
  • Ability to effectively communicate with our clients at all levels of the organizations and primarily within the laboratory

About Labcorp

At Labcorp, we are a global leader of innovative and comprehensive laboratory services that helps doctors, hospitals, pharmaceutical companies, researchers and patients make clear and confident decisions.

Through our unparalleled diagnostics and drug development laboratory capabilities, our nearly 70,000 employees combine cutting-edge innovation, science and technology to solve some of today's biggest health challenges, accelerate life-changing healthcare breakthroughs and impact lives around the world.

Here, you are empowered to own your career journey and create a personalized development plan with the support of your team.

Benefits:Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible toparticipatein the 401(k) Plan only. For more detailed information, pleaseclick here.

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.

We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit ouraccessibility siteor contact us atLabcorp Accessibility. Formore information about how we collect and store your personal data, please see ourPrivacy Statement.


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