Test Method Validation Engineer Duration: 6 Months Location: On-site at San Diego, CA Only W2 ... Key Responsibilities: • Conduct GR&R, TMV, and measurement system analysis. • Drive process ...
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Test Method Validation Engineer Duration: 6 Months Location: On-site at San Diego, CA Only W2 ... Key Responsibilities: • Conduct GR&R, TMV, and measurement system analysis. • Drive process ...
Quick apply
Test Method Validation Engineer Duration: 6 Months Location: On-site at San Diego, CA Only W2 ... Key Responsibilities: • Conduct GR&R, TMV, and measurement system analysis. • Drive process ...
Cincinnati, OH · On-site
$28 - $31/hr
This position will support analytical method validation, optimization, laboratory troubleshooting, and quality initiatives across manufacturing and external laboratory partners. This is an excellent ...
Cincinnati, OH · On-site
$28 - $31/hr
This position will support analytical method validation, optimization, laboratory troubleshooting, and quality initiatives across manufacturing and external laboratory partners. This is an excellent ...
Execute analytical method transfer, verification, validation, and troubleshooting activities supporting both biologic and small molecule pharmaceutical products. * Perform routine and non-routine ...
Execute analytical method transfer, verification, validation, and troubleshooting activities supporting both biologic and small molecule pharmaceutical products. * Perform routine and non-routine ...
Execute analytical method transfer, verification, validation, and troubleshooting activities supporting both biologic and small molecule pharmaceutical products. * Perform routine and non-routine ...
Execute analytical method transfer, verification, validation, and troubleshooting activities supporting both biologic and small molecule pharmaceutical products. * Perform routine and non-routine ...
Execute analytical method transfer, verification, validation, and troubleshooting activities supporting both biologic and small molecule pharmaceutical products. * Perform routine and non-routine ...
Execute analytical method transfer, verification, validation, and troubleshooting activities supporting both biologic and small molecule pharmaceutical products. * Perform routine and non-routine ...
Execute analytical method transfer, verification, validation, and troubleshooting activities supporting both biologic and small molecule pharmaceutical products. * Perform routine and non-routine ...
Execute analytical method transfer, verification, validation, and troubleshooting activities supporting both biologic and small molecule pharmaceutical products. * Perform routine and non-routine ...
Execute analytical method transfer, verification, validation, and troubleshooting activities supporting both biologic and small molecule pharmaceutical products. * Perform routine and non-routine ...
Execute analytical method transfer, verification, validation, and troubleshooting activities supporting both biologic and small molecule pharmaceutical products. * Perform routine and non-routine ...
Rockville, MD · On-site
... analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the Validation Engineer must be ...
Rockville, MD · On-site
... analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the Validation Engineer must be ...
... validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the ...
... validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the ...
Rockville, MD · On-site
... analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the Validation Engineer must be ...
Rockville, MD · On-site
... analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the Validation Engineer must be ...
Completes method development, validations, USP/NF method verification, method transfers, and various laboratory support functions. Provide essential analytical support to various projects, ensuring ...
Completes method development, validations, USP/NF method verification, method transfers, and various laboratory support functions. Provide essential analytical support to various projects, ensuring ...
Completes method development, validations, USP/NF method verification, method transfers, and various laboratory support functions. Provide essential analytical support to various projects, ensuring ...
Completes method development, validations, USP/NF method verification, method transfers, and various laboratory support functions. Provide essential analytical support to various projects, ensuring ...
Completes method development, validations, USP/NF method verification, method transfers, and various laboratory support functions. Provide essential analytical support to various projects, ensuring ...
Completes method development, validations, USP/NF method verification, method transfers, and various laboratory support functions. Provide essential analytical support to various projects, ensuring ...
Execute analytical method qualification and validation studies supporting release, stability, characterization and in process testing of cell therapy products in a GMP environment. * Independently ...
Execute analytical method qualification and validation studies supporting release, stability, characterization and in process testing of cell therapy products in a GMP environment. * Independently ...
Carlsbad, NM · On-site
$114K - $211K/yr
... validation for assays and devices used in clinical and GMP laboratory settings ... As a trusted quality leader, you will shape how analytical methods are brought to life in a highly ...
Carlsbad, NM · On-site
$114K - $211K/yr
... validation for assays and devices used in clinical and GMP laboratory settings ... As a trusted quality leader, you will shape how analytical methods are brought to life in a highly ...
Rockville, MD · On-site
... validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the ...
Quick apply
Rockville, MD · On-site
... validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the ...
Analytical research and development activities will include literature searches, analytical method development, test procedure writing, analytical method validation, and method transfer. Analyzes ...
Analytical research and development activities will include literature searches, analytical method development, test procedure writing, analytical method validation, and method transfer. Analyzes ...
$114K - $211K/yr
... validation for assays and devices used in clinical and GMP laboratory settings ... As a trusted quality leader, you will shape how analytical methods are brought to life in a highly ...
$114K - $211K/yr
... validation for assays and devices used in clinical and GMP laboratory settings ... As a trusted quality leader, you will shape how analytical methods are brought to life in a highly ...
Completes method development, validations, USP/NF method verification, method transfers, and various laboratory support functions. Provide essential analytical support to various projects, ensuring ...
Completes method development, validations, USP/NF method verification, method transfers, and various laboratory support functions. Provide essential analytical support to various projects, ensuring ...
Rockville, MD · On-site
... validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the ...
Quick apply
Rockville, MD · On-site
... validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the ...
$22.60 - $27.64
2% of jobs
$27.64 - $32.69
6% of jobs
$32.69 - $37.74
13% of jobs
$39.32 is the 25th percentile. Wages below this are outliers.
$37.74 - $42.79
13% of jobs
$42.79 - $47.84
11% of jobs
The median wage is $50.36 / hr.
$47.84 - $52.88
12% of jobs
$52.88 - $57.93
9% of jobs
$61.82 is the 75th percentile. Wages above this are outliers.
$57.93 - $62.98
13% of jobs
$62.98 - $68.03
13% of jobs
$68.03 - $73.08
6% of jobs
$73.08 - $78.13
3% of jobs
$22
$51
$78
To thrive in Analytical Method Validation, you need a strong background in analytical chemistry or related sciences, precision in laboratory work, and experience with method development and validation protocols, often supported by a relevant degree. Familiarity with instrumentation such as HPLC, GC, and mass spectrometry, as well as knowledge of regulatory standards like ICH, FDA, or USP, and proficiency in laboratory information management systems (LIMS) are key. Attention to detail, critical thinking, and effective communication are important soft skills for troubleshooting and collaborating with cross-functional teams. These skills ensure robust, compliant analytical methods that underpin product quality and regulatory approval.
An Analytical Method Validation job involves developing, assessing, and documenting laboratory methods to ensure they produce reliable and accurate results. Professionals in this role validate methods according to regulatory guidelines (such as ICH, USP, or FDA) by evaluating parameters like accuracy, precision, specificity, and robustness. They work in industries like pharmaceuticals, biotechnology, and chemicals to ensure compliance with quality standards. The role also requires troubleshooting analytical issues and maintaining validation records to support regulatory audits.
A typical day in Analytical Method Validation involves developing and executing protocols to verify that laboratory methods are reliable, accurate, and consistent with industry regulations. You'll spend time in the lab conducting experiments, analyzing sample data, documenting results, and preparing detailed validation reports for regulatory submission. Collaborating with quality assurance, regulatory teams, and other scientists is common to address findings and ensure alignment with project goals. This role combines hands-on technical work with critical data review and cross-disciplinary teamwork, offering a dynamic and intellectually engaging work environment.

Contractor
Posted 24 days ago
DivIHN (pronounced “divine”) is a CMMI ML3-certified Technology and Talent solutions firm. Driven by a unique Purpose, Culture, and Value Delivery Model, we enable meaningful connections between talented professionals and forward-thinking organizations. Since our formation in 2002, organizations across commercial and public sectors have been trusting us to help build their teams with exceptional temporary and permanent talent.
Visit us at https://divihn.com/find-a-job/ to learn more and view our open positions.
DivIHN is an equal opportunity employer. DivIHN does not and shall not discriminate against any employee or qualified applicant on the basis of race, color, religion (creed), gender, gender expression, age, national origin (ancestry), disability, marital status, sexual orientation, or military status.
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Software development
51 - 200 Employees
Hoffman Estates, IL, US
2002