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Contract Method Validation Jobs (NOW HIRING)

Kelly ® Engineering is seeking Validation Specialist for contract position at manufacturing client ... TMV (test method validation) * Creation SOPs * Protocols and reports on IQ/OQ/PQ * Supplier ...

... method validation and advance their careers. Job Type & Location This is a Contract position based out of Sanford, NC. Pay and Benefits The pay range for this position is $30.00 - $45.00/hr.

Apply Early

San Diego, CA Duration: 7 Month Assignment Validation Engineer- Contract Abbott Rapid Diagnostics ... method validation and process validation. * Writes and/or revises IQ, OQ, PQ related documents ...

Quality Engineer

Dorado, PR · On-site

$25 - $35/hr

... contract Objective Support multiple new line development projects by executing Tool Qualifications (TQFs), Operational Qualification (OQ), Performance Qualification (PQ), Test Method Validation (TMV ...

NC · On-site

$111K - $149K/yr

Design, lead, execute and coordinate analytical method validation and technology transfer activities within internal QC laboratories and external contract laboratories * Author and review analytical ...

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$22

$51

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How much do contract method validation jobs pay per hour?

As of Jul 4, 2026, the average hourly pay for contract method validation 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.

What is the difference between Contract Method Validation vs Analytical Method Validation?

AspectContract Method ValidationAnalytical Method Validation
PurposeValidates that a contracted method meets specific requirements for a particular project or clientEnsures an analytical method is accurate, reliable, and reproducible for testing purposes
ScopeTypically project-specific, focusing on methods used under contractual agreementsBroader, covering method development, validation, and routine testing
CredentialsOften requires validation expertise, GMP knowledge, and industry-specific certificationsRequires analytical chemistry knowledge, validation experience, and relevant certifications
Work EnvironmentPharmaceutical, biotech, or manufacturing settings with client-specific projectsLaboratories performing routine testing and method development in similar industries

Contract Method Validation focuses on validating methods for specific client projects, while Analytical Method Validation ensures the overall reliability of testing methods used routinely in laboratories. Both roles require similar credentials and work in related environments, but their scope and purpose differ.

What cities are hiring for Contract Method Validation jobs? Cities with the most Contract Method Validation job openings:
What are the most commonly searched types of Method Validation jobs? The most popular types of Method Validation jobs are:
What states have the most Contract Method Validation jobs? States with the most job openings for Contract Method Validation jobs include:
Infographic showing various Contract Method Validation job openings in the United States as of June 2026, with employment types broken down into 89% Full Time, and 11% Part Time. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.
Contract Method Development Scientist - Surface Chemistry

Contract Method Development Scientist - Surface Chemistry

LifeSprout

Baltimore, MD • On-site

Contractor

Posted 6 days ago

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Job description

Contract Method Development Scientist
About LifeSprout
LifeSprout is a medical device company developing innovative biomaterial products for aesthetic and reconstructive medicine. Our synthetic biomaterial platform is designed to mimic the look and behavior of native tissue and is being advanced into products intended to restore form and function for patients with soft tissue loss. We are seeking a highly capable contract scientist to support a focused analytical method development and validation project in a fast-paced, hands-on environment.

Position Overview
LifeSprout is opening a short-term contract role (approximately 2–3 months) for a hands-on Method Development Scientist to lead improvement and validation of a colorimetric analytical method, specifically an Ellman’s assay for quantification of surface bound thiol groups . This role requires a strong analytical chemistry background and the ability to independently assess an underdeveloped assay, improve its performance, and deliver a validated method package suitable for internal use. The ideal candidate brings deep experience in colorimetric or spectrophotometric assay development, method troubleshooting, and formal validation in a regulated environment.

Key Responsibilities
  • Assess, troubleshoot, and improve an existing colorimetric assay, including identification of factors affecting sensitivity, robustness, and reproducibility.
  • Design and execute method development experiments to optimize assay conditions, sample preparation, reagents, and analytical parameters.
  • Improve method performance with emphasis on sensitivity, precision, and practical limits of detection and quantitation.
  • Plan, author, and execute method validation protocols and generate defensible validation reports.
  • Draft and revise SOPs, work instructions, and supporting technical documentation required for internal method implementation.
  • Summarize data clearly, interpret results scientifically, and recommend next steps based on sound analytical reasoning.
  • Collaborate cross-functionally as needed while operating with a high degree of independence in a short-term contract setting.
  • Deliver a complete, validated method package ready for internal laboratory use.

Required Qualifications
  • PhD or MS with significant relevant experience in Analytical Chemistry, Chemistry, Chemical Engineering, Materials Science, Biomedical Engineering, or a related scientific discipline.
  • Demonstrated hands-on experience in analytical method development, optimization, and validation in regulated laboratory environments such as medical device, biotechnology, pharmaceutical, or GMP/ISO 13485 settings.
  • Strong analytical chemistry background with direct experience in colorimetric and/or spectrophotometric method development.
  • Experience improving assay sensitivity, precision, and overall robustness, including work related to LOD/LOQ or comparable performance characteristics.
  • Direct experience authoring and executing validation protocols, SOPs, work instructions, and validation reports.
  • Knowledge of validation concepts such as accuracy, precision, linearity, range, specificity, and robustness.
  • Knowledge of statistical approaches for method evaluation, acceptance criteria, and data analysis.
  • Excellent technical writing, data interpretation, and troubleshooting skills.
  • Ability to work independently with minimal oversight and drive work to completion on an accelerated timeline.

Working Conditions and Logistics
This is an on-site contract position based in Baltimore, Maryland, with an expected duration of approximately 2–3 months. The role requires regular laboratory presence and a high level of hands-on execution. The successful candidate will be expected to move quickly, apply strong scientific judgment, and deliver high-quality technical documentation and validated results within a short project timeline.

Eligibility
Eligibility to work in the U.S. is required.

LifeSprout offers the opportunity to make a direct technical impact on an important analytical development project supporting innovative biomaterial products.
This position is best suited for a scientist who combines strong experimental ownership with deep analytical chemistry expertise and proven success in colorimetric method development and validation.
We are looking for someone who can quickly assess, improve, validate, and document a method with minimal supervision in a contract setting.

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