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Lab Instrument Validation Engineer Jobs (NOW HIRING)

Centstone

Lab Instrument Support Engineer

Rahway, NJ · On-site

Job Title : Sr Lab Instrument Support Engineer Location : Rahway, NJ Requirements:   *   A minimum of 8 years work experience in GXP / Analytical lab environment.   *   Experience ...

Etched

Power Validation Engineer

San Jose, CA · On-site

Job Summary We are looking for a Power Validation Engineer to own the end-to-end power ... lab instrument fluency (triggering on rare transient events, correlating multi-channel captures ...

The Consensus

Power Validation Engineer

San Jose, CA · On-site

Job Summary We are looking for a Power Validation Engineer to own the end-to-end power ... lab instrument fluency (triggering on rare transient events, correlating multi-channel captures ...

Etched

Power Validation Engineer

San Jose, CA · On-site

Job Summary We are looking for a Power Validation Engineer to own the end-to-end power ... lab instrument fluency (triggering on rare transient events, correlating multi-channel captures ...

Etched

Power Validation Engineer

San Jose, CA · On-site

Job Summary We are looking for a Power Validation Engineer to own the end‑to‑end power ... and lab instrument fluency (triggering on rare transient events, correlating multi‑channel ...

Semtech

Silicon Validation Engineer

San Diego, CA · On-site

The Silicon Validation Engineer will create test plans, run and analyze lab measurements, author ... Write scripts and instrument drivers to automate the validation. Leverage AI-assisted development ...

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Lab Instrument Validation Engineer information

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How much do lab instrument validation engineer jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for lab instrument validation engineer 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.

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For Lab Instrument Validation Engineer jobs, the most frequently searched job titles are:

Senior CSV / Lab Instrument Validation Consultant

Foster City, CA • On-site

Adeptsource
11 - 50 employees
Learn more about Adeptsourceexternal

Full-time

Re-posted 9 days ago

Job description

Sr. CSV / Lab Instrument Validation Specialist
Type of role: Contract
Duration: 12-36+ months
Hourly pay rate: DOE (C2C, W2, or 1099 permissible)
Location: South San Francisco Bay Area (Remote during COVID)
Our customer is seeking a Senior CSV / Lab Instrument Validation Engineer who is well versed in laboratory Instrument processes within a Pharmaceutical environment. Must have hands experience on Lab Instrument Qualification.You will be primarily responsible for planning, leading, and executing validation efforts for standalone Lab Instrument Software systems.
Must have strong experience in the following:
  • Responsible for performing validation of Laboratory Instrumentation by following approved standard operating procedures (SOPs), current Good Manufacturing Practices (GMPs) and all other regulatory requirements.
  • Responsible for the mapping and bringing consistency to theinstrument lifecycle globally,from supporting purchase to instrument validation to decommissioning documentation.
  • Plan, lead, and execute the standardizing of validation efforts for standalone Lab Instrument Software systems.
  • Responsible for developing and executing on validation plans according to approved procedures, collation of test results, and organizes data packages and maintains all documentation pertaining to validation.
  • Ability to compile and analyze validation data, prepare reports and makes recommendations for changes and/or improvements.
  • Well versed in Laboratory Instrument process, ability to provide guidance to management on what improvements need to be made. (Essential for this role)
  • May also investigate and trouble-shoot problems which occur, and determine solutions.
  • Support change management and manage existing lab systems.
  • Participates on cross-functional project teams with the support of Development, Quality, and other groups
  • Familiar with FDA guidelines for Instrument and Software validation.
  • Experience must come from a pharmaceutical, biotech industry with direct knowledge of FDA regulations including 21CFR Part 11.
  • Self-motivated, good communication, technical writing, presentation skills, detail oriented, analytical, and a team player.

Dawn West
AdeptSource

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