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Laboratory Instrument Validation Consultant Jobs

JobFormance

LABORATORY TECHNOLOGIST

Hackettstown, NJ · On-site

Minimum five years experience in Hematology and Coagulation preferably, experience with instrument validations, correlations and training lab staff on new laboratory instrumentation. Experience: The ...

iLocatum

LABORATORY TECHNOLOGIST

Hackettstown, NJ · On-site

Minimum five years experience in Hematology and Coagulation preferably, experience with instrument validations, correlations and training lab staff on new laboratory instrumentation. Experience: The ...

Integrated Resources INC

Validation Engineer

Durham, NC · On-site

Previous experience with validation of laboratory instrument systems preferred. Reviews validation deliverables created by others for adherence to site validation SOPs and acts as validation approver ...

W3Global Inc.

Medical Lab Scientist

Chicago, IL

$32 - $36/hr

Perform routine instrument maintenance and basic troubleshooting. * Assist with new instrument installations and assay validations. * Use the Laboratory Information System (LIS) to manage daily ...

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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.

LABORATORY TECHNOLOGIST

Hackettstown, NJ • On-site

SteveRecruiter, LLC
Recruiting and Staffing Services • 1 - 10 employees
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Posted 19 days ago

Job description

Laboratory Technologist

Education Experience:

B.S. Medical Technology/Clinical Laboratory Science or equivalent from an accredited four-year college or university required.

MT(ASCP) Certification or equivalent preferred.

Minimum five years experience in Hematology and Coagulation preferably, experience with instrument validations, correlations and training lab staff on new laboratory instrumentation.

Experience:

The Laboratory Technologist is involved with clinical trial regulations in order to provide input to clinical trial designs and execution. Assist in conducting and supporting R&D activities and clinical trials, in development of new Hematology and Hemostasis product launches. You will verify technical conditions prior to the start of a study. Working with members of the service operations team, create good logistical conditions for clinical studies, which include delivery of reagents and/or instrument, specimens, exchange of correspondence, contracts, and administrative documents.

Additional duties & requirements include:

  • Ensure full understanding of the protocol requirements to ensure the study proceeds efficiently in order to meet organizational time lines.
  • Work closely with the NCRA for all necessary study follow-up in accordance with defined procedure, including but not limited to the checklist for site initiation and monitoring visits, etc.
  • Ensure corrective actions are followed for proper conduct to freeze databases of results in accordance with the studies initial objectives.
  • Check completeness of records (all forms of media: paper and electronic), ensure centralization and formatting of data from studies, as well as ensuring traceability of data.
  • Use knowledge and experience with instrument validation, interference, on-board stability, Limit of Blank, Limit of Detection, Limit of quantification to perform Linearity and Method Comparison testing.
  • Maintain laboratory equipment following daily, weekly and monthly maintenance schedules as well as required quality control for all laboratory analyzers.
  • Participates in validation of new equipment as appropriate.
  • Assist the NCRA's in the development and maintenance of clinical study binders and utilization of eCRF.
  • Manages the Laboratory equipment service contracts and documentary elements of clinical trial activities;
  • Completes necessary clinical trial documentation from the site's perspective, in preparation of study start up.
  • Give scientific presentations as required.
  • Offer support on new product launches as needed.

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