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Validation Engineer Part Time Jobs in California

Field Engineer

Petaluma, CA ยท On-site

$36 - $41/hr

Field Engineer - Part Time Equal Opportunity Employer/Veterans/Disabled SUMMARY : Provide field ... Valid current Driver's License required. * Ability to travel, as needed, for projects. SUPERVISORY ...

Field Engineer

Petaluma, CA ยท On-site

$36 - $41/hr

Field Engineer - Part Time Equal Opportunity Employer/Veterans/Disabled SUMMARY : Provide field ... Valid current Driver's License required. * Ability to travel, as needed, for projects. SUPERVISORY ...

Manufacturing Engineer

San Jose, CA ยท Remote

$85K - $110K/yr

Air Aviation is seeking a Manufacturing Engineer to support client projects on a part-time remote ... Support the development, testing, and validation of mechanical systems, assemblies, and components.

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San Luis Obispo, CA Employment Type: Part-Time About Praxis Engineering: Praxis is a civil and ... Valid Class C driver's license for occasional site visits Why Praxis: We're a small firm with a ...

Senior Process Engineer, Water

Walnut Creek, CA ยท On-site

$115K - $148K/yr

Valid California Professional Engineering license, or Professional Engineering license in another ... Regular full-time and part-time employees (working at least 20 hours per week) have access to ...

Project Engineer I

Los Angeles, CA ยท On-site

$80K - $95K/yr

A current and valid Certificate of Registration as an Architect by the California Architectural ... Arcadis offers benefits for full time and part time positions. These benefits include medical ...

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Validation Engineer Part Time information

See California salary details

$22

$51

$77

How much do validation engineer part time jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for validation engineer part time 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 Validation Engineer Part Time job?

A Validation Engineer in a part-time role is responsible for testing and verifying that products, systems, or processes meet regulatory and quality standards. They work in industries like pharmaceuticals, manufacturing, or software, ensuring compliance with industry regulations. Part-time validation engineers may focus on specific projects, conduct tests, analyze data, and create reports while working fewer hours than a full-time position. This role requires strong analytical skills, attention to detail, and knowledge of industry guidelines. It offers flexibility while maintaining a critical role in quality assurance and compliance.

What are the key skills and qualifications needed to thrive in the Validation Engineer Part Time position, and why are they important?

To thrive as a Validation Engineer Part Time, you need a solid background in engineering, quality assurance, and regulatory standards, often supported by a relevant degree in engineering or a related technical field. Familiarity with validation protocols, data acquisition tools, and industry-specific software such as statistical analysis and document management systems is typically required. Strong analytical thinking, attention to detail, and effective communication are standout soft skills in this position. These skills are essential to ensure products or processes meet stringent quality standards while efficiently coordinating with cross-functional teams on a part-time schedule.

What are the typical responsibilities of a part-time Validation Engineer?

As a part-time Validation Engineer, your primary responsibilities usually include developing and executing validation protocols, analyzing testing data, and documenting results to comply with industry standards and regulations. You may also assist in troubleshooting issues, collaborating closely with quality assurance, manufacturing, or R&D teams to ensure processes or products meet required specifications. The part-time structure often means handling specific projects or validation phases, making time management and prioritization crucial. This role is ideal for professionals seeking flexibility while still contributing technical expertise to critical validation activities.

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 Validation Engineer Part Time jobs in California? For Validation Engineer Part Time jobs in California, the most frequently searched job titles are:
What job categories do people searching Validation Engineer Part Time jobs in California look for? The top searched job categories for Validation Engineer Part Time jobs in California are:
What cities in California are hiring for Validation Engineer Part Time jobs? Cities in California with the most Validation Engineer Part Time job openings:
Infographic showing various Validation Engineer Part Time job openings in California as of June 2026, with employment types broken down into 100% Part Time. Highlights an 100% In-person job distribution, with an average salary of $106,736 per year, or $51.3 per hour.

Validation Engineer

Eliquent Life Sciences, Inc

Montrose, CA โ€ข On-site

$95K - $110K/yr

Full-time, Part-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago


Job description

ELIQUENT Life Sciences is the leading global consulting firm providing solutions to life science companies researching, developing, and manufacturing innovative products to serve patients and respond to public health challenges around the world. ELIQUENT is committed to serving clientsโ€™ needs with extensive expertise, unwavering integrity, and strategic insight in a manner that supports availability of safe, effective, and high-quality drugs, biologics, and medical devices. For more information, please visit our website at eliquent.com.

Description:

We are seeking a highly skilled Commissioning, Qualification, and Validation (CQV) Engineer to join our consulting team. The CQV Engineer will play a crucial role in ensuring the successful commissioning, qualification, and validation of facilities, equipment, and processes in the pharmaceutical, biotechnology, and medical device industries. The ideal candidate will possess strong technical expertise, project management skills, and a thorough understanding of regulatory requirements.

Key Responsibilities:

  • Develop and execute commissioning and qualification protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) of Facilities and Utilities (air handling units, HVAC)
  • Coordinate and oversee the installation, testing, and validation of equipment and systems
  • Ensure compliance with regulatory guidelines (FDA, EMA, etc.) and industry standards (GMP, GxP)
  • Conduct environmental monitoring performance qualification
  • Prepare and review validation documentation, including Validation Master Plans (VMP), User Requirement Specifications (URS), and risk assessments
  • Perform validation activities for processes, systems, and equipment, including writing and executing test plans and reports
  • Identify and resolve deviations and non-conformities, ensuring timely corrective actions
  • Communicate effectively with clients, project teams, and stakeholders to ensure project objectives are met
  • Provide technical guidance and mentorship to junior team members
  • Contribute to the development and implementation of best practices and standard operating procedures (SOPs) in CQV activities
  • Stay current with industry trends, technological advancements, and regulatory changes

Requirements

  • BS in Engineering, Science or equivalent technical degree.
  • Experience with EMPQ and temperature mapping.
  • Solid understanding of GMP regulations and industry standards.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and collaboratively in a dynamic team environment.
  • Experience in commissioning, qualification, and validation within the pharmaceutical and/or medical device industry commensurate with the level of the project demand.
  • Strong analytical and problem-solving skills with attention to detail.
  • Understand and translate requestorโ€™s strategies into plans, and be able to drive the project to completion


Benefits

What We Offer:

Competitive Compensation: Attractive salary and comprehensive benefits package for full-time and part-time employees, including health, dental, vision, and life insurance, a 401(k) plan with employer match, a generous paid time off policy, and additional perks. Compensation is commensurate with professional experience.

Career Development: Opportunities for professional growth and advancement within a supportive and innovative environment.

Work-Life Balance: Flexible work arrangements and a commitment to maintaining a healthy work-life balance.

Eliquent Life Sciences is proud to be an Equal Opportunity Employer, committed to employee diversity.