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Lab Equipment Validation Analyst Jobs (NOW HIRING)

Rambus

Technical Director Validation

Johns Creek, GA · On-site

$160K - $298K/yr

Develop scripts for automating lab equipment and for analyzing lab data. * Lead validation tasks on bench planning, preparation, characterization execution, methodology improvements. * Work with ...

Rambus

Technical Director Validation

Johns Creek, GA · Hybrid

$160K - $298K/yr

Develop scripts for automating lab equipment and for analyzing lab data. * Lead validation tasks on bench planning, preparation, characterization execution, methodology improvements. * Work with ...

Rambus

Technical Director Validation

Johns Creek, GA · Hybrid

$160K - $298K/yr

Develop scripts for automating lab equipment and for analyzing lab data. * Lead validation tasks on bench planning, preparation, characterization execution, methodology improvements. * Work with ...

FruitSmart Inc

LAB TECH

Grandview, WA · On-site

$21.08 - $23.55/hr

... cleaning the lab equipment, and verification/validation of sanitation in the plant. KEY ... Understanding and being able analyze all products including but not limited to juices, purees, dry ...

ClinDCast LLC

Silicon Validation Engineer

San Jose, CA · On-site

$35 - $40/hr

We are looking for a Silicon Validation Engineer with experience in hardware validation and board ... Use lab equipment including Oscilloscope, DAQ, Multi-meter, Power Supply, and Logic Analyzer.

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Lab Equipment Validation Analyst information

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How much do lab equipment validation analyst jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for lab equipment validation analyst in the United States is $27.48, according to ZipRecruiter salary data. Most workers in this role earn between $19.71 and $32.69 per hour, depending on experience, location, and employer.

What is a lab equipment validation analyst?

A Lab Equipment Validation Analyst is a professional responsible for ensuring that laboratory instruments and equipment function according to regulatory standards and manufacturer specifications. They design and execute validation protocols, perform risk assessments, and document test results to confirm that equipment consistently produces reliable and accurate data. This role is essential in regulated industries like pharmaceuticals, biotechnology, and medical devices, where compliance with quality standards is critical. Analysts also troubleshoot equipment issues, work closely with quality assurance teams, and help maintain compliance with regulatory agencies such as the FDA or EMA.

What are the key skills and qualifications needed to thrive as a lab equipment validation analyst?

To thrive as a Lab Equipment Validation Analyst, you need a strong background in laboratory sciences, quality assurance, and regulatory compliance, often supported by a degree in a scientific field. Familiarity with validation protocols, GMP guidelines, and specialized software such as LIMS or validation lifecycle management tools is essential. Strong analytical thinking, attention to detail, and effective communication are crucial soft skills for this role. These skills ensure that laboratory equipment operates reliably and meets regulatory standards, safeguarding data integrity and product quality.

What are some common challenges faced by lab equipment validation analysts when ensuring compliance with regulatory standards?

Lab Equipment Validation Analysts often encounter challenges such as keeping up with evolving regulatory requirements (like FDA or GMP guidelines), managing tight project deadlines, and ensuring that complex technical documentation is complete and accurate. They must also coordinate with multiple departments, such as Quality Assurance and Engineering, to gather necessary data and resolve discrepancies. Staying organized and maintaining clear communication are key to overcoming these challenges and ensuring equipment remains in compliance throughout its lifecycle.

What is the difference between Lab Equipment Validation Analyst vs Lab Quality Assurance Specialist?

AspectLab Equipment Validation AnalystLab Quality Assurance Specialist
Required CertificationsGxP validation, GMP/GLP knowledgeGxP compliance, GMP/GLP familiarity
Work EnvironmentLaboratories, validation teamsQuality departments, labs
Industry UsagePharmaceutical, biotech, biotech manufacturingPharmaceutical, biotech, clinical labs

The Lab Equipment Validation Analyst primarily focuses on validating laboratory equipment to ensure compliance with industry standards, while the Lab Quality Assurance Specialist oversees overall quality processes, including audits and compliance. Both roles require similar certifications and work in laboratory settings within the pharmaceutical and biotech industries, but their core responsibilities differ in scope and focus.

What are popular job titles related to Lab Equipment Validation Analyst jobs?

For Lab Equipment Validation Analyst jobs, the most frequently searched job titles are:

Infographic showing various Lab Equipment Validation Analyst job openings in the United States as of September 2026, with employment types broken down into 69% Full Time, 5% Part Time, 2% Temporary, 19% Contract, and 5% Nights. Highlights an 100% In-person job distribution, with an average salary of $57,166 per year, or $27.5 per hour.

Validation Specialist / Calibration Technician (CQV, GMP, Life Sciences)

San Antonio, TX • On-site

VBB
See more jobs at VBBexternal

$65K - $85K/yr

Full-time

Re-posted 15 days ago

Job description

Validation Specialist / Calibration Technician (CQV, GMP, Life Sciences)
  • Location: Texas
  • Salary: $65-85K + Bonus + Benefits

Are you looking to build a career in validation, commissioning, and qualification (CQV) within the pharmaceutical / life sciences industry? We're hiring a Validation Specialist / Calibration Technician who wants hands-on experience across IQ, OQ, PQ, exposure to real projects, and a clear path into leadership. This is an opportunity to grow quickly in a GMP-regulated environment, working alongside experienced engineers while taking ownership of meaningful validation work.
What You'll Do
  • Execute and support IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols
  • Work on validation of lab systems, equipment, and utilities
  • Partner with engineering, validation teams, and lab stakeholders
  • Assist with project scheduling, coordination, and resource planning
  • Support commissioning & qualification (CQV) activities across projects
  • Contribute to GMP / GxP documentation and compliance efforts
  • Learn to lead validation workstreams and progress into a Validation Engineer / Project Lead role
What We're Looking For
  • 2+ years of experience in:
    • Validation Engineering
    • CQV (Commissioning, Qualification, Validation)
    • or GMP-regulated environments (Pharma / Biotech)
  • Strong understanding of:
    • GMP / GxP / FDA regulations
    • Validation lifecycle (IQ/OQ/PQ)
  • Ability to work cross-functionally with engineering, QA, and operations teams
  • Strong communication and problem-solving skills
  • Coachable, driven, and motivated to grow into leadership
Requirements
  • Bachelor's degree in Engineering, Life Sciences, or related field
  • Willingness to travel regionally (project-based work)
  • Experience with validation documentation, protocols, and execution
Nice to Have
  • Experience with lab systems, utilities, or manufacturing equipment validation
  • Exposure to commissioning activities (C&Q / CQV)
  • Familiarity with AI tools for validation or documentation
Why This Role
  • Hands-on experience across pharma validation projects
  • Clear path into senior validation or project leadership roles
  • Work alongside experienced engineers in regulated environments
  • Real ownership early in your career

Validation Engineer, Validation Specialist, CQV Engineer, Commissioning Engineer, Qualification Engineer, GMP Validation, GxP, IQ OQ PQ, Pharmaceutical Validation, Life Sciences Validation, Equipment Validation, Utilities Validation, Computer System Validation, CSV Engineer, FDA Compliance, GMP Engineer
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