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Validation Engineer Jobs in Anaheim, CA (NOW HIRING)

BioPhase Solutions

Validation Engineer

Los Angeles, CA · On-site

$115K/yr

We are currently looking for a Validation Engineer to work for a leading Greater Los Angeles area contract development and manufacturing organization. Salary: $100-115k+/year depending on experience ...

Valspec

Validation Engineer

Los Angeles, CA

$90K - $110K/yr

Validation Engineer (CQV) El Segundo, CA | Onsite | 6-Month Project | Start Date: November 2, 2026 Valspec | Life Sciences Commissioning, Qualification & Validation Experts Based on Valspec's CQV and ...

New

Valspec

Validation Engineer

Long Beach, CA · On-site

$90K - $110K/yr

Validation Engineer (CQV) El Segundo, CA | Onsite | 6-Month Project | Start Date: November 2, 2026 Valspec | Life Sciences Commissioning, Qualification & Validation Experts Based on Valspec's CQV and ...

New

Experis

Electronics Validation Engineer

Irvine, CA · On-site

As a Electronics Validation Engineer, you will be part of the Electronics Test and Validation department supporting vehicle electronics validation and characterization. The ideal candidate will ...

3B Staffing LLC

Validation Engineer

Irvine, CA · Hybrid

Ensure appropriate systems are in place to evaluate changes to validated/qualified systems, maintaining their validated/qualified state. * Utilize quality engineering tools, statistical methods ...

3B Staffing LLC

Validation Engineer

Irvine, CA · Hybrid

Ensure appropriate systems are in place to evaluate changes to validated/qualified systems, maintaining their validated/qualified state. * Utilize quality engineering tools, statistical methods ...

3B Staffing LLC

Validation engineer

Irvine, CA · Hybrid

Ensure appropriate systems are in place to evaluate changes to validated/qualified systems, maintaining their validated/qualified state. * Utilize quality engineering tools, statistical methods ...

3B Staffing LLC

Validation engineer

Irvine, CA · Hybrid

Ensure appropriate systems are in place to evaluate changes to validated/qualified systems, maintaining their validated/qualified state. * Utilize quality engineering tools, statistical methods ...

Cryoport, Inc.

Validation Engineer

Irvine, CA · On-site

$108 - $132/hr

The Validation Engineer - Consulting Services will support the Consulting Services team's offerings around shipper, packaging, and shipping lane qualifications across temperature sensitive supply ...

Cryoport Systems, LLC

Validation Engineer

Irvine, CA · On-site

$108 - $132/hr

Position Summary The Validation Engineer - Consulting Services will support the Consulting Services team's offerings around shipper, packaging, and shipping lane qualifications across temperature ...

Cryoport

Validation Engineer

Irvine, CA · On-site

The Validation Engineer - Consulting Services will support the Consulting Services team's offerings around shipper, packaging, and shipping lane qualifications across temperature sensitive supply ...

Cryoport, Inc.

Validation Engineer

Irvine, CA · On-site

The Validation Engineer - Consulting Services will support the Consulting Services team's offerings around shipper, packaging, and shipping lane qualifications across temperature sensitive supply ...

Eldorado CA

Validation Engineer III

Riverside, CA · On-site

$110K - $130K/yr

Validation Engineer III Location: Riverside, CA Salary Range: $110,000 - $130,000 Position Summary The Validation Engineer III will be responsible for planning, executing, and managing test and ...

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Validation Engineer information

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How much do validation engineer jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for validation engineer in Anaheim, CA is $54.44, according to ZipRecruiter salary data. Most workers in this role earn between $41.25 and $66.20 per hour, depending on experience, location, and employer.

What is a validation engineer?

A validation engineer is responsible for testing equipment and electrical systems used in the manufacturing process. As a validation engineer, your primary duty is to work with the other members of the validation team to ensure that these systems measure up to company and industry standards. Skills needed for a validation engineer job include the ability to accurately test, measure, and calibrate manufacturing equipment for maximum efficiency and quality.

What are the key skills and qualifications needed to thrive as a validation engineer, and why are they important?

To thrive as a Validation Engineer, you need a solid background in engineering, quality assurance, and regulatory compliance, typically backed by a degree in engineering or a related field. Familiarity with validation protocols, statistical analysis tools, and industry-specific regulations such as FDA, GMP, or ISO standards is essential. Strong analytical thinking, attention to detail, and effective communication set top performers apart in this role. These skills ensure that products and processes meet stringent quality and safety standards, minimizing risks and ensuring regulatory approval.

What are some common challenges validation engineers face when working cross-functionally with other departments?

Validation Engineers frequently collaborate with teams such as manufacturing, quality assurance, and research & development. One common challenge is aligning differing priorities and timelines between departments, which can sometimes delay validation projects. Effective communication skills and flexibility are crucial to navigating these cross-functional interactions, ensuring that all regulatory and quality requirements are met without hindering production schedules. Building strong working relationships and proactively addressing potential concerns can help Validation Engineers facilitate smoother project execution.

What is the difference between Validation Engineer vs Quality Assurance Engineer?

AspectValidation EngineerQuality Assurance Engineer
CertificationsGMP, ISO, Six SigmaISO, Six Sigma, CQA
Work EnvironmentRegulated industries like pharma, biotech, medical devicesManufacturing, software, and product development
Primary FocusEnsuring products meet specifications through validation processesPreventing defects through process and system improvements
Common UsageRegulatory compliance, validation protocolsProcess audits, quality systems

Validation Engineers focus on verifying that products and processes meet regulatory standards through validation protocols, especially in regulated industries. Quality Assurance Engineers concentrate on maintaining overall product quality by implementing and auditing quality systems. While both roles aim to ensure product safety and efficacy, Validation Engineers are more involved in validation activities, whereas QA Engineers focus on process improvement and defect prevention.

Is validation engineer a good job?

Validation engineers are responsible for ensuring that products and processes meet quality standards through testing and documentation, often in regulated industries like pharmaceuticals or manufacturing. The role typically requires attention to detail, knowledge of validation protocols, and familiarity with tools like GxP or FDA regulations. It can offer stable employment and opportunities for specialization and advancement.

What degree do you need to be a validation engineer?

Validation engineers typically hold a bachelor's degree in engineering, life sciences, or a related field. Some roles may require a master's degree or specialized certifications in quality assurance or validation processes. Strong knowledge of industry standards and experience with validation tools are also important.
More about Validation Engineer jobs

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Validation Engineer jobs near you
Infographic showing various Validation Engineer job openings in Anaheim, CA as of August 2026, with employment types broken down into 92% Full Time, 5% Part Time, and 3% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $113,225 per year, or $54.4 per hour.

Validation Engineer

BioPhase Solutions

Los Angeles, CA • On-site

$115K/yr

Full-time

Re-posted 24 days ago

Job description

BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Validation Engineer to work for a leading Greater Los Angeles area contract development and manufacturing organization.

Salary: $100-115k+/year depending on experience

Responsibilities:
  • Draft and Review User Requirement Specifications (URS): Develop and refine URS for new and existing process equipment, ensuring alignment with manufacturing needs and regulatory standards.
  • Perform Equipment Qualifications (IQ, OQ, PQ): Plan, execute, and document qualification protocols to verify equipment performance meets cGMP requirements and intended use.
  • Execute Process Validation and Cleaning Validation: Identify critical process parameters, establish validation protocols, and conduct cleaning validations to maintain product quality and regulatory compliance.
  • Generate and Maintain Validation Documentation: Prepare, review, and archive validation reports, SOPs, protocols, and related records to ensure clear traceability and audit readiness.
  • Troubleshoot and Investigate Deviations: Collaborate with cross-functional teams to diagnose equipment and process issues, implement corrective actions (CAPA), and address audit observations promptly.
  • Support Scale-Up and Technology Transfer Efforts: Work with manufacturing and development groups to optimize processes, facilitate seamless scale-up, and transfer validated methods across company sites.
  • Coordinate with Cross-Functional Teams: Engage Quality, Process Development, and Manufacturing teams to meet project timelines, drive continuous improvement, and uphold cGMP standards.
Experience/Requirements:
  • Bachelors in engineering, chemistry, or related field
  • Certifications related to GMP compliance, quality systems, or validation preferred.
  • 1–3+ years of experience in validation engineering or a closely related field in a cGMP-regulated pharma or biotech environment.
  • Strong working knowledge of process validation, equipment qualification (IQ/OQ/PQ), and pharmaceutical manufacturing processes.
  • Proficiency in drafting and reviewing validation documents (URS, SOPs, protocols, reports).
  • Familiarity with deviation investigations, CAPA processes, and audit responses.
  • Basic vendor management skills to evaluate and coordinate with external equipment/service providers.
  • Competence in using data analysis tools and MS Office applications to track and report validation results. 
Please send resumes to mia@biophaseinc.com and visit our website at www.biophaseinc.com for additional job opportunities!!!