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Internship Computer System Validation Csv Jobs in Arizona

Rivian

Manager - Autonomy Systems Validation

Wittmann, AZ · On-site

$148K - $186K/yr

S. degree in Automotive, Mechanical, Electrical, SW, Mechatronics, Robotics, Aerospace, Systems or Computer Science / Engineering or a strong technical background in a related field. * Valid US ...

Rivian

Manager - Autonomy Systems Validation

Wittmann, AZ · On-site

$148K - $186K/yr

S. degree in Automotive, Mechanical, Electrical, SW, Mechatronics, Robotics, Aerospace, Systems or Computer Science / Engineering or a strong technical background in a related field. * Valid US ...

GDIT

$88K - $115K/yr

Ability to conduct system integration testing and analyze new technology sets, * Experience using enterprise lab environments for validation and assessment. Location is Onsite. GDIT IS YOUR PLACE At ...

AEG

Sr. Solutions Engineer - Mulesoft

Scottsdale, AZ · On-site

$55.50 - $71.75/hr

... XML, CSV, and other payload formats. • Configure and manage API deployments to CloudHub ... Computer Science, Information Systems, Engineering, or related technical field preferred. • 3-5 ...

AXS

Sr. Solutions Engineer - Mulesoft

Scottsdale, AZ

$55.75 - $71.75/hr

Develop DataWeave transformations for JSON, XML, CSV, and other payload formats. * Configure and ... Computer Science, Information Systems, Engineering, or related technical field preferred. * 3-5 ...

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Internship Computer System Validation Csv information

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.

What are the most commonly searched types of Computer System Validation Csv jobs in Arizona?

The most popular types of Computer System Validation Csv jobs in Arizona are:

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For Internship Computer System Validation Csv jobs in Arizona, the most frequently searched job titles are:

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Cities in Arizona with the most Internship Computer System Validation Csv job openings:

Internship Computer System Validation Csv jobs near you
Infographic showing various Internship Computer System Validation Csv job openings in Arizona as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, and 4% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution.

Computer System Validation Engineer

Katalyst Healthcares and Lifesciences

Phoenix, AZ • On-site

Other

Posted 4 days ago

Job description

Job Description:
  • In this role, you will collaborate with cross-functional teams to ensure systems meet quality standards and regulatory requirements through a risk-based approach. This position focuses on maintaining data integrity and system lifecycle management while contributing to operational efficiency.

Responsibilities:
  • pply quality standards and cGMP requirements to validate computer systems, including hardware, software, procedures, and training.
  • Ensure system validation aligns with Data Integrity principles (ALCOA) and includes appropriate testing strategies.
  • Facilitate risk assessments to identify validation deliverables and project requirements.
  • Collaborate with Quality Assurance and other teams to optimize processes such as change management, backup policies, configuration management, and periodic reviews.
  • Develop and execute validation documentation, including requirements, user acceptance testing, SOPs, system impact assessments, traceability matrices, protocols, and reports.
  • nalyze validation data and troubleshoot issues in collaboration with technical teams.
  • Maintain communication with stakeholders to address system needs, validation progress, and related concerns.

Requirements:
  • Experience in validation, IT quality assurance, quality control, biomanufacturing, clinical, or regulatory operations.
  • Hands-on experience in validating computerized systems.
  • Strong understanding of pharmaceutical industry regulatory compliance, particularly US and EU/MHRA data integrity guidance.
  • bility to work effectively in a dynamic, cross-functional team environment.
  • Proven expertise in applying data governance measures and creating impactful data visualizations.
  • Preferred experience with tools and systems such as UPLC, HPLC, HIAC, qPCR, NanoDrop, TOC Analyzer, Osmometer, Cell Counters, and Excel spreadsheet validation.
  • Bachelor's degree in computer science, Engineering, Biological Sciences, or a related field.

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