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Part Time Validation Analyst Jobs (NOW HIRING)

Review and analyze test data, including airflow, temperature, pressure, and system responses, to ... Regular full-time and part-time employees (working at least 20 hours per week) have access to ...

Validation Intern

Rockville, MD ยท On-site

$35/hr

Experience using basic statistical tools or Excel-based data analysis. Location: Various Client ... Pharmaceutical & Biotechnology Internship Type: Part-Time or Full-Time, Paid Internship Duration: 2 ...

The Part-time Payroll Analyst position is eligible for remote work based on company requirements ... Validate timekeeping data, resolve discrepancies, and ensure proper documentation for each pay ...

The Part-time Payroll Analyst position is eligible for remote work based on company requirements ... Validate timekeeping data, resolve discrepancies, and ensure proper documentation for each pay ...

Validation Intern Fall 2026

Northwood, OH ยท On-site

$17 - $22.25/hr

Strong analytical and problem solving aptitude * Ability to work in team environments ... Ability to work part-time during non co-op semesters * Advanced Microsoft Excel skills * Hands-on ...

Validation Intern Fall 2026

Northwood, OH ยท On-site

$17 - $22.25/hr

Strong analytical and problem solving aptitude * Ability to work in team environments ... Ability to work part-time during non co-op semesters * Advanced Microsoft Excel skills * Hands-on ...

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Part Time Validation Analyst information

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

As of Jun 26, 2026, the average hourly pay for part time validation analyst in the United States is $31.53, according to ZipRecruiter salary data. Most workers in this role earn between $25.24 and $35.82 per hour, depending on experience, location, and employer.
What are the most commonly searched types of Validation Analyst jobs? The most popular types of Validation Analyst jobs are:

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 27 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.