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Contract Validation Engineer Jobs in California (NOW HIRING)

BioPhase Solutions

Validation Engineer

Los Angeles, CA

$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 ...

Fladger Associates

Validation Engineer

Fremont, CA · On-site

Fremont, CA Contract Duration: 3-24 months Rate: Negotiable Responsibilities: * Excellent employment opportunity for a Validation Engineer in the Fremont, CA area. * Manage and participate actively ...

Tailored Management

Validation Engineer

Vacaville, CA · On-site

$52/hr

Validation Engineer - Onsite Location: 1000 New Horizons Way, Vacaville, CA 95688 Contract: 12+ months contract with potential for extension and/or permanent placement Schedule:Monday Friday, 8:00 AM ...

TEKsystems

Validation Engineer

Roseville, CA

$65 - $100/hr

About the Role We are seeking an experienced System Validation Engineer to join a team responsible ... Job Type & Location This is a Contract position based out of Roseville, CA. Pay and Benefits The ...

TEKsystems

Validation Engineer

Roseville, CA · On-site

$65 - $100/hr

About the Role We are seeking an experienced System Validation Engineer to join a team responsible ... Job Type & Location This is a Contract position based out of Roseville, CA. Pay and Benefits The ...

KBR

Test & Validation Engineer

El Segundo, CA · Hybrid

KBR is seeking a Test & Validation Engineer to support the MSEIT contract at Space Systems Command (SSC). This role supports the program's testing and validation activities across multiple software ...

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How much do contract validation engineer jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for contract validation engineer in California is $51.32, according to ZipRecruiter salary data. Most workers in this role earn between $38.89 and $62.40 per hour, depending on experience, location, and employer.

What is a contract validation engineer?

A Contract Validation Engineer is responsible for ensuring that systems, processes, and products meet regulatory and contractual requirements. They typically work on a temporary or project basis, verifying compliance through testing, documentation, and analysis. Their role involves collaborating with engineering teams to validate designs, troubleshoot issues, and ensure quality standards are met. This position is common in industries like pharmaceuticals, aerospace, and manufacturing, where strict validation protocols are required.

What are the primary responsibilities of a contract validation engineer on a typical project?

A Contract Validation Engineer is primarily responsible for reviewing and verifying that project deliverables, processes, and products comply with contractual requirements and industry standards. This includes conducting thorough documentation reviews, performing technical validations, and collaborating with project managers, legal teams, and quality assurance professionals to resolve any discrepancies. You will also support audits, maintain compliance records, and participate in meetings to ensure all stakeholders remain informed and aligned. The role often involves both independent analysis and teamwork, providing an excellent environment for those who enjoy balancing technical expertise with cross-functional collaboration.

What are the key skills and qualifications needed to thrive in the contract validation engineer position, and why are they important?

To thrive as a Contract Validation Engineer, you need strong analytical skills, a degree in engineering or a related field, and a deep understanding of contract requirements and industry regulations. Proficiency with validation software, quality management systems (QMS), and relevant certifications such as Six Sigma or ISO standards is often preferred. Outstanding attention to detail, effective communication, and the ability to work collaboratively across departments are crucial soft skills. These competencies ensure accurate contract assessments, regulatory compliance, and seamless integration of contractual obligations into engineering projects.

What are the most commonly searched types of Validation Engineer jobs in California?

The most popular types of Validation Engineer jobs in California are:

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

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

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

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

What cities in California are hiring for Contract Validation Engineer jobs?

Cities in California with the most Contract Validation Engineer job openings:

Contract Validation Engineer jobs near you
Infographic showing various Contract Validation Engineer job openings in California as of August 2026, with employment types broken down into 87% Full Time, 8% Part Time, and 5% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $106,736 per year, or $51.3 per hour.

Validation Engineer

BioPhase Solutions

Los Angeles, CA

$115K/yr

Full-time

Re-posted 14 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!!!