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Computer System Validation Manager Jobs in Hammond, IN

Lead computer system validation (CSV) activities of Tempus AI applications, software tools, and ... Support Change Management and Major Incidents (MI) processes, ensuring organizational compliance ...

Lead computer system validation (CSV) activities of Tempus AI applications, software tools, and ... Support Change Management and Major Incidents (MI) processes, ensuring organizational compliance ...

And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact ... This position reports to the Process Validation Manager and is part of the Technical Operations ...

... Management (EWM) * Experience in computer system validation, authoring CSV deliverables, execution of testing, resolving of defects. * 3+ years manufacturing industry experience prefered * Ability to ...

Experience in validation of analytical instrument systems (e.g. benchtop analytical systems ... Manage change controls necessary for project life cycle through process compliance and interface ...

... entry, data validation, computer equipment and communication. RESPONSIBILITIES: * Transmits ... Perform e-statement system processing. * Complete batch processing for the Trust and Pension ...

... entry, data validation, computer equipment and communication. RESPONSIBILITIES: * Transmits ... Perform e-statement system processing. * Complete batch processing for the Trust and Pension ...

... entire system, take ownership of projects, and develop skills outside your comfort zone ... Accounting, Engineering, Data Processing/Analytics/Science, Computer and Information Science ...

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Computer System Validation Manager information

See Hammond, IN salary details

$45.7K

$101.5K

$154.5K

How much do computer system validation manager jobs pay per year?

As of Jul 13, 2026, the average yearly pay for computer system validation manager in Hammond, IN is $101,490.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,700.00 and $127,100.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Computer System Validation Manager, and why are they important?

To thrive as a Computer System Validation Manager, you need expertise in computer system validation regulations (such as GxP, FDA 21 CFR Part 11), strong project management skills, and a background in life sciences or IT. Familiarity with validation lifecycle documentation tools, quality management systems (QMS), and compliance software is often required, along with relevant certifications like PMP or CSV-related credentials. Exceptional attention to detail, analytical thinking, and effective communication are crucial soft skills for coordinating cross-functional teams and ensuring regulatory compliance. These skills and qualifications are vital to ensure validated systems meet regulatory standards, minimize compliance risks, and support organizational quality objectives.

What are some common challenges a Computer System Validation Manager faces during system implementation projects?

A Computer System Validation Manager often encounters challenges such as aligning validation activities with evolving regulatory requirements, managing tight project timelines, and coordinating between multiple stakeholders like IT, Quality Assurance, and business users. Ensuring thorough documentation and traceability, while adapting to technology updates or scope changes, can also be demanding. Proactive communication and strong project management skills are essential to mitigate risks and ensure successful, compliant system implementations.

What does a Computer System Validation Manager do?

A Computer System Validation Manager is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals or biotechnology, meet all required compliance standards. They oversee the planning, execution, and documentation of validation activities to ensure systems are reliable, accurate, and secure. Their duties include managing validation projects, writing protocols, coordinating with IT and quality assurance teams, and ensuring adherence to regulations like FDA 21 CFR Part 11. This role is critical for maintaining product quality and regulatory compliance.

What is the difference between Computer System Validation Manager vs Computer System Validation Specialist?

AspectComputer System Validation ManagerComputer System Validation Specialist
CertificationsGAMP, CQE, CSQEGAMP, CQE, CSQE
Work EnvironmentManagement, oversight, strategic planningExecution, testing, documentation
Industry UsagePharmaceutical, biotech, regulated industriesPharmaceutical, biotech, regulated industries
Primary FocusLeading validation projects, team coordinationPerforming validation activities, testing

The main difference between a Computer System Validation Manager and a Computer System Validation Specialist lies in their roles. The manager oversees validation projects, manages teams, and ensures compliance, while the specialist executes validation tasks and documents testing procedures. Both roles require similar certifications and are vital in regulated industries like pharmaceuticals and biotech.

What job categories do people searching Computer System Validation Manager jobs in Hammond, IN look for? The top searched job categories for Computer System Validation Manager jobs in Hammond, IN are:
What cities near Hammond, IN are hiring for Computer System Validation Manager jobs? Cities near Hammond, IN with the most Computer System Validation Manager job openings:

Validation Engineer (CQV, GMP, Life Sciences)

VBB

Chicago, IL • On-site

$70K - $100K/yr

Full-time

Re-posted 19 days ago


Job description

Validation Engineer (CQV, GMP, Life Sciences)
  • Location: Greater Chicago
  • Salary: $70-100K + Bonus + Benefits
  • No Sponsorship, No Relocation

Are you looking to build a career in validation, commissioning, and qualification (CQV) within the pharmaceutical / life sciences industry? We're hiring a Validation Engineer who wants hands-on experience across IQ, OQ, PQ, exposure to real projects, and a clear path into leadership. This is an opportunity to grow quickly in a GMP-regulated environment, working alongside experienced engineers while taking ownership of meaningful validation work.
What You'll Do
  • Execute and support IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols
  • Work on validation of lab systems, equipment, and utilities
  • Partner with engineering, validation teams, and lab stakeholders
  • Assist with project scheduling, coordination, and resource planning
  • Support commissioning & qualification (CQV) activities across projects
  • Contribute to GMP / GxP documentation and compliance efforts
  • Learn to lead validation workstreams and progress into a Validation Project Lead role
What We're Looking For
  • 5+ years of experience in:
    • Validation Engineering
    • CQV (Commissioning, Qualification, Validation)
    • or GMP-regulated environments (Pharma / Biotech)
  • Strong understanding of:
    • GMP / GxP / FDA regulations
    • Validation lifecycle (IQ/OQ/PQ)
  • Ability to work cross-functionally with engineering, QA, and operations teams
  • Strong communication and problem-solving skills
  • Coachable, driven, and motivated to grow into leadership
Requirements
  • Bachelor's degree in Engineering, Life Sciences, or related field
  • Willingness to travel regionally (project-based work)
  • Experience with validation documentation, protocols, and execution
Nice to Have
  • Experience with lab systems, utilities, or manufacturing equipment validation
  • Exposure to commissioning activities (C&Q / CQV)
  • Familiarity with AI tools for validation or documentation
Why This Role
  • Hands-on experience across pharma validation projects
  • Clear path into senior validation or project leadership roles
  • Work alongside experienced engineers in regulated environments

Validation Engineer, Validation Specialist, CQV Engineer, Commissioning Engineer, Qualification Engineer, GMP Validation, GxP, IQ OQ PQ, Pharmaceutical Validation, Life Sciences Validation, Equipment Validation, Utilities Validation, Computer System Validation, CSV Engineer, FDA Compliance, GMP Engineer
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