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Computer Validation Jobs in Walnut, CA (NOW HIRING)

The Validation Manager works with Quality, Manufacturing, Maintenance, Sanitation, and Regulatory ... This position requires strong communication skills, computer skills, and experience in management.

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 ...

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 ...

Validation Manager

Corona, CA · On-site

$95K - $105K/yr

The Validation Manager works with Quality, Manufacturing, Maintenance, Sanitation, and Regulatory ... This position requires strong communication skills, computer skills, and experience in management.

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 ...

Validation Engineer

Los Angeles, CA · On-site

$80K - $90K/yr

Computer literacy with proficiency in MS Office (Outlook, Word, Excel, PowerPoint) * Must be ... Validation Engineer role based in California, is $80,000 - $90,000.Additionally, the position is ...

Validation Engineer

Los Angeles, CA · On-site

$80K - $90K/yr

Computer literacy with proficiency in MS Office (Outlook, Word, Excel, PowerPoint) * Must be ... Validation Engineer role based in California, is $80,000 - $90,000. Additionally, the position is ...

Design test procedures, test fixtures, and validation protocols for mechanical systems and ... Proficient with Microsoft Office Suite and CAD software. What you'll receive for the great work you ...

The Model Validation Director is expected to lead and execute model validation testing processes on ... Computer Science, Management Information Systems, or Statistics/Mathematics. * Experience with data ...

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See Walnut, CA salary details

$10

$55

$87

How much do computer validation jobs pay per hour?

As of Jun 2, 2026, the average hourly pay for computer validation in Walnut, CA is $55.35, according to ZipRecruiter salary data. Most workers in this role earn between $42.64 and $65.67 per hour, depending on experience, location, and employer.

What is the difference between Computer Validation vs Quality Assurance Specialist?

AspectComputer ValidationQuality Assurance Specialist
Required CredentialsGxP, 21 CFR Part 11, validation certificationsISO standards, QA certifications, GxP knowledge
Work EnvironmentPharmaceutical, biotech, regulated industriesManufacturing, healthcare, regulated industries
Employer & Industry UsageRegulated industries requiring validated systemsEnsuring quality compliance across processes

Computer Validation focuses on verifying that computer systems meet regulatory requirements and function correctly, primarily in regulated industries. Quality Assurance Specialists oversee overall quality processes, ensuring compliance and standards across various operations. While both roles require knowledge of GxP and industry regulations, Computer Validation is more technical and system-specific, whereas QA Specialists have a broader scope in quality management.

What cities near Walnut, CA are hiring for Computer Validation jobs? Cities near Walnut, CA with the most Computer Validation job openings:
Computer System Validation Engineer

Computer System Validation Engineer

Avid Bioservices

Tustin, CA • On-site

$82K - $104.40K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 14 days ago


Job description

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 Engineer is 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 that comply 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.