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Internship Computer System Validation Csv Jobs (NOW HIRING)

Inteldot

WI · On-site

$125 - $150/hr

Position Summary We are seeking an experienced Senior Computer System Validation (CSV) Engineer to support validation activities for GMP-regulated manufacturing and automation systems at client. The ...

ClinDCast LLC

CSV Consultant

Raritan, NJ · On-site

$150 - $200/hr

Perform Computer System Validation (CSV) activities for SAP ERP, WMS, and enterprise applications. * Develop and execute validation documentation, including Validation Plans, Requirements, Test ...

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

As of Sep 8, 2026, the average hourly pay for internship computer system validation csv in the United States is $51.80, according to ZipRecruiter salary data. Most workers in this role earn between $38.94 and $64.42 per hour, depending on experience, location, and employer.

What is an internship in computer system validation (CSV)?

An Internship in Computer System Validation (CSV) is a temporary position, typically for students or recent graduates, that provides hands-on experience in ensuring that computer systems used in regulated industries (like pharmaceuticals or healthcare) meet required standards and regulations. Interns assist with validating software and hardware, documenting processes, and ensuring compliance with industry guidelines such as FDA 21 CFR Part 11 or EU Annex 11. This role helps interns understand the lifecycle of computer systems in a regulated environment and prepares them for careers in quality assurance, compliance, or IT within highly regulated sectors.

What are the typical responsibilities of an intern in computer system validation (CSV)?

As a Computer System Validation (CSV) intern, you can expect to assist with tasks such as reviewing and drafting validation documentation, executing test scripts, and collecting evidence to ensure compliance with regulatory requirements. You may also support the maintenance of validation records and participate in team meetings to discuss project progress or findings. These responsibilities are crucial in ensuring that computer systems used in regulated industries, like pharmaceuticals or healthcare, function as intended and meet quality standards. Working closely with senior validation specialists, you'll gain hands-on experience with industry guidelines and learn how cross-functional teams collaborate to achieve compliance.

What are the key skills and qualifications needed for an internship in computer system validation (CSV)?

To thrive as an Internship Computer System Validation CSV specialist, you need foundational knowledge in computer science, life sciences, or engineering, along with an understanding of regulatory standards like GxP or FDA 21 CFR Part 11. Familiarity with validation documentation, software testing tools, and quality management systems is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for interpreting requirements and collaborating with cross-functional teams. These skills ensure compliance, data integrity, and the successful validation of computerized systems in regulated environments.

What is the difference between Internship Computer System Validation Csv vs Computer System Validation Specialist?

AspectInternship Computer System Validation CsvComputer System Validation Specialist
CredentialsTypically pursuing or recent graduate, basic understanding of validationRelevant certifications (e.g., GAMP, ISPE), experience preferred
Work EnvironmentInternship setting, supervised, entry-level tasksFull-time role, independent responsibilities in regulated industries
Industry UsageUsed in pharmaceutical, biotech, and medical device companies for trainingUsed for maintaining compliance, validating systems in regulated environments

In summary, the Internship Computer System Validation Csv is an entry-level position focused on learning and supporting validation tasks, while the Computer System Validation Specialist is a more experienced role responsible for ensuring system compliance and validation in regulated industries.

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Internship Computer System Validation Csv jobs near you
Infographic showing various Internship Computer System Validation Csv job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, and 2% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $107,747 per year, or $51.8 per hour.

Computer System Validation (CSV) Specialist

Wilson, NC • On-site

Validation & Engineering Group, Inc
See more jobs at Validation & Engineering Group, Incexternal

Full-time

Posted 8 days ago

Key responsibilities

  • Support the validation and lifecycle management of GxP computerized systems.

  • Develop, review, and execute validation documentation including URS, specifications, risk assessments, validation plans, protocols, test scripts, traceability matrices, and validation summary reports.

  • Support system implementation, upgrades, enhancements, periodic reviews, and participate in audit and inspection readiness activities.

Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Computer System Validation Specialist

Position Summary

We are seeking a Computer System Validation (CSV) Specialist/Engineer to support validation activities for computerized systems in a regulated manufacturing environment. The ideal candidate will have 3–4 years of hands-on CSV experience and a solid understanding of GxP requirements, system lifecycle documentation, and data integrity principles.

Key Responsibilities

  • Support the validation and lifecycle management of GxP computerized systems.
  • Develop, review, and execute validation documentation, including:
    • User Requirements Specifications (URS)
    • Functional/Design Specifications
    • Risk Assessments
    • Validation Plans
    • IQ/OQ/PQ protocols
    • Test Scripts
    • Traceability Matrices
    • Validation Summary Reports
  • Execute and document system testing and ensure appropriate resolution of discrepancies and deviations.
  • Support system implementation, upgrades, enhancements, and periodic reviews.
  • Perform computerized system risk assessments in accordance with applicable regulatory requirements and company procedures.
  • Ensure compliance with 21 CFR Part 11, GxP, data integrity, and electronic records/electronic signature requirements.
  • Collaborate with IT, Engineering, Quality, Manufacturing, Automation, and system owners throughout the system lifecycle.
  • Support change controls, deviations, CAPAs, and system retirement activities as applicable.
  • Assist with audit and inspection readiness activities related to computerized systems.
  • Maintain accurate and complete validation documentation in accordance with approved procedures.

Qualifications

  • Bachelor’s degree in Engineering, Computer Science, Information Technology, Life Sciences, or a related technical discipline.
  • 3–4 years of experience in Computer System Validation (CSV) within a regulated environment, preferably pharmaceutical, biotechnology, medical device, or life sciences manufacturing.
  • Working knowledge of GAMP 5, 21 CFR Part 11, GxP, and data integrity principles.
  • Experience developing and executing computerized system validation documentation and testing.
  • Strong documentation, analytical, and problem-solving skills.
  • Ability to work cross-functionally with technical and quality teams.
  • Strong written and verbal communication skills.

Preferred Qualifications

  • Experience with Power BI for dashboards, reporting, data visualization, or analytics.
  • Experience validating manufacturing, laboratory, quality, or enterprise systems.
  • Experience supporting system upgrades, implementation projects, or digital transformation initiatives.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.