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Laboratory Instrument Validation Consultant Jobs

ASK Consulting

CSV/CQV Validation Specialist

Bend, OR · On-site

... laboratory instrument and equipment qualification activities. • Perform other duties as assigned ... systems validation and equipment qualification. • Experience managing multiple validation ...

New

Novo Nordisk A/S

The Position Works closely with Laboratory personnel to support repairs, preventive maintenance ... Understand & execute GMP & compliance protocols for instrument validation * Executes work according ...

Ashland

Quality Control Analytical Chemist

Hopewell, VA · On-site

Monitors and resolves laboratory data drifts and trends. * Perform non-routine testing for the purposes of new instrument validation or method transfers. * Develops analytical method equivalency and ...

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How much do laboratory instrument validation consultant jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for laboratory instrument validation consultant in the United States is $58.47, according to ZipRecruiter salary data. Most workers in this role earn between $51.44 and $65.14 per hour, depending on experience, location, and employer.

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Infographic showing various Laboratory Instrument Validation Consultant job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 14% Part Time, and 6% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $121,624 per year, or $58.5 per hour.

Senior CSV / Lab Instrument Validation Consultant

Foster City, CA • On-site

Adeptsource
11 - 50 employees
Learn more about Adeptsourceexternal

Full-time

Re-posted 12 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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