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Lab Equipment Validation Analyst Jobs (NOW HIRING)

Synopsys

Silicon Validation Engineer

Hillsboro, OR · On-site

At Synopsys, you will validate SerDes PHYs that power the systems running the world, and the lab ... Hands-on experience with lab equipment including oscilloscopes, network analyzers, signal ...

Bio-Techne Corp.

$55K - $91K/yr

Prepare COAs for Original Equipment Manufacturer (OEM) customers. * Reviews all copies ... Experience: 3-5 years of related experience in a lab or quality assurance setting. * Experience in ...

Noblesoft Technologies

Validation Engineer

Austin, TX · On-site

Hands on experience in using high-end lab equipment like Power supplies, Oscilloscopes, Spectrum Analyzers etc.. * Experience in Power validation at Board level and silicon level * Deep knowledge of ...

Synopsys, Inc.

At Synopsys, you will validate SerDes PHYs that power the systems running the world, and the lab ... Hands-on experience with lab equipment including oscilloscopes, network analyzers, signal ...

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Lab Equipment Validation Analyst information

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$10

$27

$47

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

As of Sep 10, 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.

Urgent On-Site Opening for Senior CQV Engineer - Needham, MA - Need Local to MA Only.

Needham, MA • On-site

SmartIPlace
IT Services • 51 - 200 employees
Learn more about SmartIPlaceexternal

Contractor

Re-posted 6 days ago

Job description

Note :

  • Need Local to MA, with same State I’d Only.

Position Overview :

  • Need someone with Lab experience.
  • We are looking for 4 Senior Commissioning, Qualification, and Validation (CQV) Engineers to perform execution of lab equipment qualification (LEQ) and facility/environmental utility (FEU) commissioning activities to support the reactivation and GMP-readiness of a Boston area client’s QC Laboratory.
  • This role will focus on drafting and executing URS, IQ, OQ, PQ, and commissioning protocols, ensuring equipment, utilities, and lab spaces are compliant with FDA/EMA requirements and fully audit-ready within a compressed five-week timeline.
  • Ideally, all candidates will be capable of working cross functionally on both equipment and the facility systems, however in terms of focus we will need two QAV engineers to handle the equipment validation and 2 Commissioning Engineers to handle the FEU validation.

Tasks, Responsibilities, and Deliverables:

  • Develop and execute URS for lab equipment and utilities (balances, centrifuges, incubators, freezers, biosafety cabinets, HVAC, gases, freezer room).
  • Draft and execute commissioning protocols for FEU systems.
  • Perform and document IQ, OQ, and PQ for lab instruments and support equipment.
  • Conduct criticality assessments to determine validation scope and depth.
  • Support traceability matrix development to ensure requirements coverage.
  • Document test execution results, deviations, and corrective actions.
  • Prepare and finalize GMP-ready validation reports for submission to QA.
  • Interface with Client SMEs and QA for review/approval cycles, ensuring alignment with site standards.
  • Deliver assigned packages within agreed milestones to enable regulatory readiness.

Required Skills, Scope, and Experience:

  • Bachelor’s degree in Engineering, Life Sciences, or related field.
  • 8+ years’ experience in commissioning, qualification, and validation within GMP-regulated biopharma/biotech environments.
  • Strong knowledge of FDA, EMA, and ICH requirements, including 21 CFR Parts 210, 211.
  • Demonstrated expertise in IQ/OQ/PQ execution for QC lab instruments and utilities.
  • Experience with commissioning HVAC, environmental monitoring systems (EMS), and building management systems (BMS).
  • Familiarity with risk-based validation (ISPE Baseline Guides, ASTM E2500).
  • Strong technical writing and documentation skills (URS, protocols, reports).
  • Ability to deliver results under compressed timelines with high compliance standards.
     
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About Smart-iPlace

Sourced by ZipRecruiter

SMART-iPLACE provides innovative staffing and consulting solutions that help our clients achieve their business objectives. We can understand and support all areas of your IT systems from back-end infrastructure to front-end personal productivity. Our goal is create innovative IT solutions that enable your business to be more agile and competitive.

Industry

It services

Company size

51 - 200 Employees

Headquarters location

Irving, TX, US

Year founded

2021

Social media

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