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Internship Computer System Validation Csv Jobs in Riverside, CA

Apple

Wireless Systems Validation Engineer

Irvine, CA

$175K - $308K/yr

We operate at the intersection of silicon development and system deployment, where rigorous ... Preferred Qualifications Advanced degree in Electrical Engineering or Computer Engineering; Master ...

Apple

Wireless Systems Validation Engineer

Irvine, CA

$122K - $214K/yr

We operate at the intersection of silicon development and system deployment, where rigorous ... Preferred Qualifications Advanced degree in Electrical Engineering or Computer Engineering; Master ...

Apple

Wireless Systems Validation Engineer

Irvine, CA

$175K - $308K/yr

We operate at the intersection of silicon development and system deployment, where rigorous ... Preferred Qualifications Advanced degree in Electrical Engineering or Computer Engineering; Master ...

Apple

Wireless Systems Validation Engineer

Irvine, CA · On-site

We operate at the intersection of silicon development and system deployment, where rigorous ... Preferred Qualifications Advanced degree in Electrical Engineering or Computer Engineering; Master ...

Apple

Wireless Systems Validation Engineer

Irvine, CA

$122K - $214K/yr

We operate at the intersection of silicon development and system deployment, where rigorous ... Preferred Qualifications Advanced degree in Electrical Engineering or Computer Engineering; Master ...

Apple

Wireless Systems Validation Engineer

Irvine, CA · On-site

We operate at the intersection of silicon development and system deployment, where rigorous ... Preferred Qualifications Advanced degree in Electrical Engineering or Computer Engineering; Master ...

Kaav Inc

SAP Project Manager-CA

La Verne, CA · On-site

Strong understanding of GxP, FDA validation, and CSV (Computer System Validation) processes. * Experience in SAP modules relevant to manufacturing and supply chain (PP, MM, WM, QM). * Excellent ...

Gilead

Sr Manager, Quality Assurance

La Verne, CA

$143K - $185K/yr

Demonstrates knowledge of Information Systems Technology, understanding of Computer System Validation (CSV) including current electronic records and signature requirements. * Knowledge of Six Sigma ...

Apple

Wireless Systems Validation Engineer

Irvine, CA

$122K - $214K/yr

We operate at the intersection of silicon development and system deployment, where rigorous ... Preferred Qualifications Advanced degree in Electrical Engineering or Computer Engineering; Master ...

Apple

Wireless Systems Validation Engineer

Irvine, CA

$175K - $308K/yr

We operate at the intersection of silicon development and system deployment, where rigorous ... Preferred Qualifications Advanced degree in Electrical Engineering or Computer Engineering; Master ...

Herbalife

Engineer, Validation

Lake Forest, CA · On-site

Basic experience with equipment cleaning and computer systems validation methodologies is a plus. * Experience in electronic validation systems is preferred but not required. * Openness to learning ...

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All JobsComputer System Validation Csv JobsInternship Computer System Validation Csv JobsInternship Computer System Validation Csv Jobs in Riverside, CA

Internship Computer System Validation Csv information

See Riverside, CA salary details

$30

$54

$78

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

As of Jul 9, 2026, the average hourly pay for internship computer system validation csv in Riverside, CA is $54.04, according to ZipRecruiter salary data. Most workers in this role earn between $40.62 and $67.21 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 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 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 job categories do people searching Internship Computer System Validation Csv jobs in Riverside, CA look for? The top searched job categories for Internship Computer System Validation Csv jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Internship Computer System Validation Csv jobs? Cities near Riverside, CA with the most Internship Computer System Validation Csv job openings:
Internship Computer System Validation Csv jobs near you
Computer System Validation Engineer

Computer System Validation Engineer

Avid Bioservices

Tustin, CA • On-site

$82K - $104K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 21 days ago

Job description

Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Your Role:
The Computer System Validation Engineeris responsible for providing technical validation support for manufacturing equipment, laboratory instruments, computer systems, networks, and software that have been newly installed, upgraded, replaced and/or modified in the cGMP Manufacturing Facility as well as its related manufacturing support areas, which may include Facilities/ Engineering, Quality Assurance, Supply Chain, and Quality Control.
  • Review and help author User Requirement Specification (URS) and/or Requirement Specification documents for manufacturing equipment/systems and processes
  • Generate and execute Installation, Operational and Performance/Process qualification (IQ, OQ, PQ) protocols, engineering studies and final reports thatcomply with corporate and regulatory requirements.
  • Coordinate and oversee validation protocol execution or validation activities with cross-functional departments.
  • Evaluate and analyze qualification data collected during projects, while verifying acceptability of the data and compliance with the approved protocol.
  • Ensure any deviations to protocols and/or deviations to acceptance criteria are adequately addressed, documented and reviewed by the Validation Committee
  • Provide input and assist on the development of validation policies and procedures.
  • Effectively interact and provide validation guidance to other departments.
  • Assist department manager in developing realistic time and resource requirements for validation activities in support of company expectation.
  • Provide input and assist in change control assessment and Part 11 assessment for validated systems.
  • Review Standard Operating Procedures (SOPs) and ensure the operational parameters described in the SOP for the equipment reflects validated conditions.
  • Assist department manager on other types of projects/managerial responsibilities as needed
Minimum Qualifications:
  • BA/BS in science (such as Biology, Microbiology, Biochemistry, Chemistry), Engineering (such as Electrical, Electronics, Computer Science) or other equivalent technology related field.
  • Minimum of 3 years' work experience in biopharmaceutical/pharmaceutical manufacturing environment of which 1 year is directly involved in validations.
Position Type/Expected Hours of Work:
This role is a full-time position. Days and hours of work are Monday through Friday, 8am to 5pm PST, unless otherwise stated by Supervisor.
Compensation:
We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
The compensation range for this role is $82,000- $104,400 annually depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
Who you are:
  • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
  • Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
  • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
  • You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.
Physical Demands & Work Environment:
In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 25 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.
Employment Type: Full-Time

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