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Internship Computer System Validation Csv Jobs (NOW HIRING)

... provides computer system validation and information technology consulting services to ... The CSV Specialist will be responsible for managing and executing all activities related to ...

PR ยท On-site

$90.10K - $118.60K/yr

The ideal candidate will have extensive expertise in validation and compliance, computer system validation (CSV), and familiarity with DeltaV, Aveeva PI. A background in the biotechnology industry is ...

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... provides computer system validation and information technology consulting services to ... The CSV Specialist will be responsible for managing and executing all activities related to ...

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Internship Computer System Validation Csv information

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

As of May 29, 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 are the key skills and qualifications needed to thrive as an Internship Computer System Validation (CSV) specialist, and why are they important?

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 are some typical responsibilities for an intern in Computer System Validation (CSV), and how do they contribute to the overall validation process?

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 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 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.

More about Internship Computer System Validation Csv jobs
What cities are hiring for Internship Computer System Validation Csv jobs? Cities with the most Internship Computer System Validation Csv job openings:
What are the most commonly searched types of Computer System Validation Csv jobs? The most popular types of Computer System Validation Csv jobs are:
What states have the most Internship Computer System Validation Csv jobs? States with the most job openings for Internship Computer System Validation Csv jobs include:
Infographic showing various Internship Computer System Validation Csv job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 84% Full Time, and 15% Part Time. Highlights an 68% Physical, 21% Hybrid, and 11% Remote job distribution, with an average salary of $107,747 per year, or $51.8 per hour.

Validation Specialist - QC Equipment (CSV Focus)

Technical and Engineering Consulting

Yauco, PR โ€ข On-site

Full-time

Posted 26 days ago


Job description

Position Overview
Technical & Engineering Consulting is seeking a Validation Specialist with strong Computer System Validation (CSV) experience to support Quality Control (QC) laboratory equipment qualification in a regulated pharmaceutical environment.
This role will focus on analytical laboratory systems, including FTIR Spectrophotometers (Identification testing) and Endotoxin testing systems (e.g., Nebula), ensuring compliance with cGMP, Data Integrity, and regulatory expectations.
Key Responsibilities
  • Execute qualification and validation activities for QC laboratory equipment and computerized systems
  • Develop and/or support protocol generation (IQ, OQ, PQ)
  • Perform protocol execution and discrepancy resolution
  • Support review and approval of validation documentation
  • Ensure compliance with CSV lifecycle requirements (GAMP 5 approach preferred)
  • Utilize electronic document management systems (EDMS) for documentation control
  • Support data integrity assessments and audit readiness
  • Collaborate with QC, QA, IT, and Validation teams
  • Ensure alignment with QC lab requirements and regulatory standards (FDA, cGMP)
Required Qualifications
  • Bachelor's degree in Microbiology, Chemistry, Engineering, or related field
  • 3-5 years of experience in validation within regulated environments (Pharma / Biotech / Medical Devices)
  • Hands-on experience with QC laboratory equipment qualification
  • Strong knowledge of Computer System Validation (CSV)
  • Experience with analytical instrumentation (e.g., FTIR, endotoxin systems)
  • Familiarity with:
    • cGMP regulations
    • Data Integrity (ALCOA+)
    • Validation lifecycle documentation
Preferred Qualifications
  • Experience with FTIR Spectrophotometer (ID testing)
  • Experience with Endotoxin testing systems (Nebula or similar)
  • Knowledge of LIMS, Empower, or other lab systems
  • Experience with TrackWise, Kneat, or similar validation systems
  • Familiarity with GAMP 5 methodology
Key Skills
  • Strong technical writing and documentation skills
  • Attention to detail and compliance mindset
  • Ability to work cross-functionally in fast-paced environments
  • Problem-solving and analytical thinking