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Internship Computer System Validation Csv Jobs in Goleta, CA

The Systems Validation Engineer designs and develops systems and software test programs for ... Education & Experience: BS in Computer Engineering, Computer Science, Physics, Electrical ...

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Community Health Worker

Santa Barbara, CA · On-site

$21.25 - $27.75/hr

Minimum: Valid California driver's license, reliable transportation, and insurance coverage as ... internship positions in a community setting. Cottage Health is a leading acute care hospital system ...

Community Health Worker

Santa Barbara, CA · On-site

$24.57 - $36.58/hr

Minimum: Valid California driver's license, reliable transportation, and insurance coverage as ... Ability to type and navigate on a computer. Years of Related Work Experience: * Minimum: Lived ...

Mentor young engineers and engineering interns. DESIRED QUALIFICATIONS: * Minimum 15+ years ... automotive safety systems * Education: BS in Computer Science, Robotics, or other relevant ...

Mentor young engineers and engineering interns. DESIRED QUALIFICATIONS: * Minimum 15+ years ... automotive safety systems * Education: BS in Computer Science, Robotics, or other relevant ...

Mentor young engineers and engineering interns. DESIRED QUALIFICATIONS: * Minimum 15+ years ... automotive safety systems * Education: BS in Computer Science, Robotics, or other relevant ...

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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 Aug 20, 2026, the average hourly pay for internship computer system validation csv in Goleta, CA is $55.89, according to ZipRecruiter salary data. Most workers in this role earn between $42.02 and $69.52 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.

What are the most commonly searched types of Computer System Validation Csv jobs in Goleta, CA?

The most popular types of Computer System Validation Csv jobs in Goleta, CA are:

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

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Cities near Goleta, CA with the most Internship Computer System Validation Csv job openings:

Business Application & Systems Administrator

Agilent

Carpinteria, CA • On-site

$116K - $219K/yr

Full-time

Re-posted 13 days ago


Agilent Technologies rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

48th of 542 rated manufacturers


Job description

Job Description

The Business Applications & Systems Administrator is responsible for managing, implementing, and optimizing business applications. The role will develop & coordinate testing with impacted departments, including specifically coordinating with IT and Quality for validation & compliance. Manages business application projects, ensuring effective communication across teams/functions as well as informing management of progress and key issues.

Key Responsibilities

Application Management:

  • Administer and maintain core business owned applications (e.g. Project & Portfolio Management, Electronic Lab Notebook, Lab Management, Image Management, Spotfire business intelligence).

Configuration & Customization:

  • Configure applications to support business workflows, including directly configuring and through available technical resources.

Compliance & Validation:

  • Write test plans and testing scripts in support of Computer System Validation (CSV) team
  • Ensure systems meet GxP, FDA 21 CFR Part 11, and other regulatory requirements as required based on application upgrades.
  • Collaborate with IT and QA on compliance and security attestations.

Support & Troubleshooting:

  • Provide first line support for application-related questions, including directing to appropriate subject matter experts.

Upgrades & Patches:

  • Plan and execute upgrades and patches and ensure validation compliance

Data Integrity:

  • Ensure data integrity and traceability across systems.

Training:

  • Train end-users and maintain user guides.
Qualifications
  • Bachelor's degree in Information Technology, Computer Science, or related field.

  • 8+ years in application administration.

  • Familiarity with validated systems and regulatory compliance.

  • Strong understanding of GxP, FDA 21 CFR Part 11 compliance.

  • Excellent problem-solving and communication skills.


Preferred Qualifications:

  • 10+ years in business applications management.

  • Experience within a life sciences environment.

  • Experience with cloud-based pharmaceutical applications.

  • Knowledge of change control in regulated environments.

  • Familiarity with CSV (Computer System Validation) processes.

  • Experience with leading cloud based business systems implementation.

Additional Details

This job has a full time weekly schedule. It includes the option to work remotely. Applications for this job will be accepted until at least August 25, 2026 or until the job is no longer posted.The full-time equivalent pay range for this position is $116,800.00 - $219,000.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locationsAgilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.Travel Required: OccasionalShift: DayDuration: No End DateJob Function: Administration

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