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Computer System Validation Jobs in Corona, CA (NOW HIRING)

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 ...

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

$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

$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 ...

The Remas Company, LLC

Project Manager

La Verne, CA · On-site

This position is also responsible for monitoring Computer System validation (CSV) as well as compliance with GxP regulations and 21 CFR Part 11. * Leads the effort to manage, and/or maintains ...

Horizontal Talent

Validation Engineer

San Clemente, CA · On-site +1

Execute system, integration, data migration, and user acceptance testing activities. * Partner ... Contribute to validation readiness and help ensure work aligns with GxP expectations and CSA ...

Nanda Technologies

CSV Engineer

Costa Mesa, CA · On-site

$55 - $60/hr

Bachelor's degree in Engineering, Computer Science, Life Sciences, or related field. * 2-10+ years of experience in computerized systems validation within pharmaceutical, biotechnology, or life ...

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All JobsComputer System Validation JobsComputer System Validation Jobs in Corona, CA

Computer System Validation information

See Corona, CA salary details

$10

$56

$88

How much do computer system validation jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for computer system validation in Corona, CA is $56.04, according to ZipRecruiter salary data. Most workers in this role earn between $43.17 and $66.44 per hour, depending on experience, location, and employer.

What is a computer system validation?

A Computer System Validation (CSV) job involves ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, meet compliance and regulatory requirements. CSV professionals develop and execute validation protocols to confirm that software, hardware, and processes function as intended and maintain data integrity. They work with quality assurance, IT, and regulatory teams to document compliance with standards like FDA 21 CFR Part 11 and GxP. This role is critical in maintaining system reliability, product quality, and patient safety.

What are the key skills and qualifications needed to thrive in computer system validation, and why are they important?

To excel in Computer System Validation, candidates typically need a background in computer science, engineering, or life sciences, with expertise in validating software and systems in regulated environments such as pharmaceuticals or medical devices. Familiarity with tools like validation documentation software, GAMP 5 guidelines, FDA 21 CFR Part 11 regulations, and potentially certifications like CSV Professional or Six Sigma is highly valued. Strong attention to detail, analytical thinking, and effective communication skills help professionals work collaboratively and document findings precisely. These abilities ensure compliance, data integrity, and the reliability of computerized systems critical to safety and quality.

What are some typical challenges faced in computer system validation roles?

Professionals in Computer System Validation often encounter challenges such as keeping up with evolving regulatory requirements, ensuring complete and accurate documentation, and coordinating with cross-functional teams to implement validation protocols. Balancing thoroughness with project deadlines can also be demanding, as every validation step must stand up to external audits. However, these challenges provide valuable experience, strengthen project management abilities, and emphasize teamwork—key attributes that support career advancement into validation leadership or quality assurance roles.

Is computer system validation a good field?

Computer System Validation (CSV) is a vital part of regulated industries like pharmaceuticals and biotech, ensuring that computer systems meet quality and compliance standards. It offers opportunities for professionals with skills in validation protocols, regulatory requirements, and tools like GxP and 21 CFR Part 11. The field provides steady employment, career growth, and the chance to work on critical quality assurance processes.

What job categories do people searching Computer System Validation jobs in Corona, CA look for?

The top searched job categories for Computer System Validation jobs in Corona, CA are:

What cities near Corona, CA are hiring for Computer System Validation jobs?

Cities near Corona, CA with the most Computer System Validation job openings:

Computer System Validation jobs near you
Infographic showing various Computer System Validation job openings in Corona, CA as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $116,566 per year, or $56 per hour.

Computer System Validation Engineer

Avid Bioservices

Tustin, CA

$82K - $104K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 2 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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