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Computer Validation Jobs in California (NOW HIRING)

Wellington Foods Inc

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.

Applied Intuition

Validation Engineer

Sunnyvale, CA · Hybrid

About the role We are looking for a skilled Validation Engineer to join our team. This role ... Bachelors in Computer Science, Engineering or any equivalent majors Nice to have: * Experience with ...

Collabera

Validation Engineer

Milpitas, CA

Must be computer literate, and detail/quality oriented. Will be trained to perform validation and prepare protocols in one or more of the following areas: facilities, utilities, equipment, computer ...

Grifols

Validation Engineer

Los Angeles, CA

$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 ...

GRIFOLS, S.A.

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 ...

Applied Intuition

Validation Engineer

Sunnyvale, CA · On-site

About the role We are looking for a skilled Validation Engineer to join our team. This role ... Bachelors in Computer Science, Engineering or any equivalent majors Nice to have: * Experience with ...

Curia, Inc.

Validation Specialist II

Camarillo, CA · On-site

$75K - $93.50K/yr

Key responsibilities include conducting computer system validations to ensure adherence to GxP regulations, including 21 CFR Parts 210, 211, and 820, as well as compliance with Good Automated ...

Oracle

Hardware Validation Engineer

Santa Clara, CA · On-site

As a Hardware Validation Engineer, you will join a collaborative team focused on defining ... Familiar with cloud server hardware, CPU/GPU computer architecture, and common computer protocols

AMRI

Validation Specialist II

Camarillo, CA

$75K - $93.50K/yr

Key responsibilities include conducting computer system validations to ensure adherence to GxP regulations, including 21 CFR Parts 210, 211, and 820, as well as compliance with Good Automated ...

PSC Biotech

Validation Engineer I

Bodega Bay, CA · On-site +1

$20 - $23/hr

Support the planning, development, and implementation of computer systems validation documentation. Write and execute required validation documentation including requirements specifications, test ...

Marvell

Principal Validation Lead

Santa Clara, CA · On-site

Bachelor's degree in Electrical Engineering, Computer Engineering, or related field. * Typically 8+ years of industry experience in silicon or system validation, including hands-on lab work. * Strong ...

PSC Biotech

Validation Engineer I

Bodega Bay, CA · On-site +1

$20 - $23/hr

Support the planning, development, and implementation of computer systems validation documentation. * Write and execute required validation documentation including requirements specifications, test ...

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Computer Validation information

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$10

$53

$84

How much do computer validation jobs pay per hour?

As of Jun 3, 2026, the average hourly pay for computer validation in California is $53.61, according to ZipRecruiter salary data. Most workers in this role earn between $41.30 and $63.56 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 are popular job titles related to Computer Validation jobs in California? For Computer Validation jobs in California, the most frequently searched job titles are:
What job categories do people searching Computer Validation jobs in California look for? The top searched job categories for Computer Validation jobs in California are:
What cities in California are hiring for Computer Validation jobs? Cities in California with the most Computer Validation job openings:
Computer Validation jobs near you
Validation Manager

Validation Manager

Wellington Foods Inc

Corona, CA • On-site

$95K - $105K/yr

Full-time

Posted 26 days ago

Job description

POSITION SUMMARY:
The Validation Manager works with Quality, Manufacturing, Maintenance, Sanitation, and Regulatory personnel to perform manufacturing process and cleaning process validations and qualification of manufacturing equipment. Job duties include developing validation plans, designing validation protocols, executing the protocols, and summarizing the validation works with validation reports. This position requires strong communication skills, computer skills, and experience in management.
The position reports to the Vice-President of Quality Systems.
MAJOR FUNCTIONS & RESPONSIBILITIES:
  • Lead the validation activities with protocol design, and execution of the protocol for OTC products manufacturing process and cleaning process validations.
  • Lead the validation activities with protocol design, and execution of the protocol for dietary supplements and food products cleaning process validations.
  • Lead validation, verification, and qualification activities on manufacturing equipment and control systems validation, verification, and qualification.
  • Responsible for the oversight of ongoing (DQ, IQ, OQ, PQ) validation activities in compliance with regulatory requirements.
  • Design, review, and approve protocols as well as reports to deliver a complete package of qualification documents.
  • When validation activities are outsourced, you will manage the activity and monitor KPIs to assure the performance and cost effectiveness.
  • Coach and grow validation team members including enhancing their performance, career development, sharing knowledge and experience, conduct training, and adhere to regulatory compliance.
  • Design overall validation strategy for the site as well as act as a technical lead.
  • Write and review GMP documents including cleaning and validation procedures, SOPs, and training documentation.
  • Work closely with Manufacturing and Scheduling to build a qualification schedule that delivers minimum interruption to manufacturing output.
  • Work in a safe manner, always ensuring full compliance to HS&E policies.
  • Take initiatives in continuous improvement of the manufacturing facility.
  • Actively maintaining up to date developments, standards, and operating practices within the Food, Dietary Supplement, and pharmaceutical industries.
  • Conduct root cause analysis to facilitate and initiate corrective actions and preventive actions (CAPA) with manufacturing operations management.
  • Develop and write standard operating procedures (SOPs) ensuring compliance with the company's policies and FDA regulations.
  • Adhere and enforce current Good Manufacturing Practices (cGMPs) and Good Documentation Practices (GDPs), safety, company rules, SOPs, and policies.
  • Willing to accept additional assignments and responsibilities by senior management.

REQUIRED EDUCATION / WORK EXPERIENCE / SKILLS:
  • Prefer a 4-year college degree (BS or BA) in science (i.e. Biology, Chemistry, Biochemistry, Microbiology, Biotechnology, and/or Engineering etc.). Engineering experience is preferred.
  • At least 5 years of work experience in pharmaceutical, personal care, biotechnology, dietary supplements, food and/or beverage industry with the knowledge of Regulatory Compliance on equipment validation, cleaning validation, and manufacturing process validation.
  • 1-2 years supervisory experience preferred.
  • Good working knowledge of 21 CFR Part 111, 21 CFR Part 117, 21 CFR Part 210 & 211.
  • Good knowledge of Hazard Analysis and Critical Control Points and other food safety programs, quality assurance and manufacturing principles and procedures.
  • Ability to communicate effectively in writing and verbally with employees at all levels of the organization.
  • Ability to manage and prioritize multiple projects using effective organizational skills and judgment in an environment of frequent new customer products.
  • Ability to use Microsoft Office applications; specifically using Word to create and modify documents, Excel to record data and calculate results, and PowerPoint to prepare training documents.

OTHER REQUIREMENTS:
  • The role-holder will be required to operate across the facility including GMP environments which requires careful attention to details, and closely following applicable SOPs.

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