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DataAnnotation

$40/hr

Benefits This is a full-time or part-time REMOTE position You'll be able to choose which projects ... engineering, DFIR, malware analysis, threat intelligence, or similar) Some coding experience ...

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

As of Jun 4, 2026, the average hourly pay for validation engineer part time in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 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.
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Validation Engineer Part Time jobs near you

Validation Engineer

Eliquent Life Sciences, Inc

Montrose, CA • On-site

$95K - $110K/yr

Full-time, Part-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 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 clients’ 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 requestor’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.