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Qa Validation Jobs in California (NOW HIRING)

PSC Biotech

Validation QA Specialist

Pomona, CA · On-site

$110 - $120/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Your Role The Validation QA Specialist is responsible for providing Quality Assurance oversight of validation documentation and ensuring compliance with applicable GMP regulations, company procedures ...

PSC Biotech

Validation QA Specialist

Pomona, CA · On-site

$110K - $120K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Your Role The Validation QA Specialist is responsible for providing Quality Assurance oversight of validation documentation and ensuring compliance with applicable GMP regulations, company procedures ...

PSC Biotech

Validation QA Specialist

Pomona, CA · On-site

$110K - $120K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Your Role The Validation QA Specialist is responsible for providing Quality Assurance oversight of validation documentation and ensuring compliance with applicable GMP regulations, company procedures ...

PSC Biotech

Validation QA Specialist

Pomona, CA

$110K - $120K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Your Role The Validation QA Specialist is responsible for providing Quality Assurance oversight of validation documentation and ensuring compliance with applicable GMP regulations, company procedures ...

Sotera Health

Quality Assurance Technician

Los Angeles, CA · On-site

$37K - $54K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Assists the Validation Coordinator with validations and calibrations. * Analyzes temperature and humidity probe data. * Other QA/Validation duties as assigned. * Maintains all quality related ...

Sotera Health

Quality Assurance Technician

Los Angeles, CA

$37K - $54K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Assists the Validation Coordinator with validations and calibrations. * Analyzes temperature and humidity probe data. * Other QA/Validation duties as assigned. * Maintains all quality related ...

360 IT Professionals

QA Engineer

San Ramon, CA

Experience interpreting and analyzing requirements to create effective test scenarios and ability to capture QA validation artifacts * Thorough understanding of development and testing life cycles ...

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All JobsQa Validation JobsQa Validation Jobs in California

Qa Validation information

What is a QA Validation professional?

QA Validation professionals are specialists responsible for ensuring that products, processes, or systems meet defined quality standards and regulatory requirements. They design and execute tests, document results, and analyze data to confirm that all specifications are met before a product is released or a process goes live. Their work is crucial in industries such as pharmaceuticals, manufacturing, and software, where compliance and consistent quality are essential. QA Validation experts help prevent defects, ensure safety, and maintain customer trust.

What are the key skills and qualifications needed to thrive as a QA Validation professional?

To thrive as a QA Validation professional, you need a solid understanding of quality assurance processes, regulatory standards (such as FDA or ISO), and a relevant science or engineering degree. Familiarity with validation protocols, documentation systems, and tools like LIMS or TrackWise is typically required, along with certifications such as ASQ CQV or similar. Attention to detail, analytical thinking, and effective communication are essential soft skills for ensuring compliance and facilitating teamwork. These competencies are critical for guaranteeing product quality, regulatory compliance, and the smooth operation of validation activities in highly regulated industries.

What are some common challenges faced by QA Validation professionals in regulated industries?

QA Validation professionals in regulated industries often face the challenge of staying current with evolving compliance standards while ensuring that all processes and documentation meet strict regulatory requirements. They must balance thorough validation activities with tight project timelines, often collaborating closely with cross-functional teams such as manufacturing, engineering, and regulatory affairs. Attention to detail and strong organizational skills are essential, as even small errors can lead to costly delays or regulatory findings. Effective communication with team members and stakeholders is also critical to ensure successful audits and product launches.

What is the difference between Qa Validation vs Qa Analyst?

AspectQa ValidationQa Analyst
CertificationsGMP, GxP, Validation certificationsGMP, GxP, Quality assurance certifications
Work EnvironmentRegulated industries like pharma, biotechPharmaceutical, biotech, manufacturing
Primary FocusValidating processes, systems, equipmentAnalyzing quality data, audits, process improvements
Employer UsageQuality validation teams in regulated industriesQuality assurance departments across industries

Qa Validation specialists focus on validating systems and processes to ensure compliance with industry standards, often working on equipment and software validation. Qa Analysts primarily analyze quality data, perform audits, and support process improvements. While both roles ensure product quality, Qa Validation emphasizes validation activities, whereas Qa Analysts focus on ongoing quality analysis and reporting.

What are popular job titles related to Qa Validation jobs in California?

For Qa Validation jobs in California, the most frequently searched job titles are:

What job categories do people searching Qa Validation jobs in California look for?

The top searched job categories for Qa Validation jobs in California are:

What cities in California are hiring for Qa Validation jobs?

Cities in California with the most Qa Validation job openings:

Qa Validation jobs near you
Infographic showing various Qa Validation job openings in California as of August 2026, with employment types broken down into 1% As Needed, 92% Full Time, 3% Part Time, and 4% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution.

Quality Assurance Validation Engineer

VTI Life Sciences

Thousand Oaks, CA • On-site

Contractor

Posted 7 days ago

Job description

Quality Assurance Validation Specialist
Position Summary
Location: Thousand Oaks, California - On-site 40 Hours a week
Assignment Duration: August 2026 through February 2027
Extension Potential: Yes
Type of Role: Full Time Employment (W2) or Contractor
Industry: Pharmaceutical/Biotechnology
Experience Level: Intermmediate, with 6+ years of relevant experience
We are seeking an experienced Quality Assurance Validation Specialist to provide quality oversight for pharmaceutical and biopharmaceutical validation activities. Working within cross-functional project teams, this role will review and approve validation deliverables and change controls to ensure facilities, systems, equipment, and processes comply with regulatory requirements, company standards, and current industry practices.
The successful candidate will support validation across facilities, utilities, manufacturing equipment, instruments, process qualification, cleaning validation, computerized systems, data integrity, and other systems used in regulated pharmaceutical environments.
Key Responsibilities
  • Review validation documents against approved Standard Operating Procedures (SOPs), regulatory requirements, and internal quality guidelines.
  • Assess validation documentation for accuracy, completeness, consistency, and GMP compliance.
  • Provide quality review and approval of documentation needed to support project execution and regulatory submissions.
  • Review and approve validation lifecycle deliverables, including:
    • Validation Master Plans
    • Design Qualification (DQ)
    • Installation Qualification (IQ)
    • Operational Qualification (OQ)
    • Performance Qualification (PQ)
    • Computer System Validation (CSV)
    • Validation maintenance packages
    • System decommissioning documentation
  • Provide validation expertise during the development or modification of manufacturing facilities, utilities, equipment, processes, information systems, and computerized systems.
  • Define, communicate, and oversee applicable Quality Assurance requirements throughout the project lifecycle.
  • Participate in project and system risk assessments.
  • Ensure requirements remain traceable throughout the complete project lifecycle.
  • Support the resolution of quality-related issues, including matters involving GMP requirements and validation compliance.
  • Review change controls and evaluate their potential impact on validated systems and processes.
  • Maintain project quality metrics and communicate risk trends, implementation readiness, and potential impacts to project timelines and commercial readiness.
  • Collaborate effectively with Engineering, Manufacturing, Quality, Validation, Automation, IT, and other project stakeholders.
  • Perform other related duties as assigned.
Qualifications
Education
  • Bachelor's degree in Biotechnology, Microbiology, Pharmacy, Engineering, Life Sciences, or a related discipline.
  • An advanced degree may be considered in combination with relevant professional experience.
Experience
  • At least six years of experience in a pharmaceutical, biopharmaceutical, biotechnology, or related regulated manufacturing environment.
  • Demonstrated experience in pharmaceutical or biotechnology validation.
  • Hands-on experience writing, reviewing, and executing validation protocols.
  • Experience reviewing qualification and validation documentation from a Quality Assurance perspective.
  • Working knowledge of GMP regulations, data integrity principles, risk-based validation, and validation lifecycle practices.
  • Experience with electronic document and validation management systems such as Veeva, Kneat, ALM, or comparable platforms.
Preferred Skills
  • Strong understanding of facilities, utilities, manufacturing equipment, laboratory instruments, cleaning validation, process qualification, and computerized system validation.
  • Familiarity with applicable FDA, EMA, ICH, GAMP 5, and other relevant regulatory or industry expectations.
  • Strong technical writing and document-review capabilities.
  • Excellent attention to detail, organization, and analytical judgment.
  • Ability to identify compliance risks and communicate practical, risk-based recommendations.
  • Strong interpersonal skills and the ability to work effectively with multidisciplinary teams.
  • Ability to manage multiple priorities in a project-driven environment.
What Success Looks Like
In this position, you will help ensure that project deliverables are inspection-ready, validation requirements are traceable, risks are identified early, and new or modified systems are ready for compliant implementation and commercial use.

Apply