Scientist, Method Validation
$46K - $96K/yr
We are seeking Scientist, Method Validation to join IQVIA Laboratories at Ithaca, NY. We hire ... Analyze laboratory data and report results accurately and within established timelines * Operate ...
$46K - $96K/yr
We are seeking Scientist, Method Validation to join IQVIA Laboratories at Ithaca, NY. We hire ... Analyze laboratory data and report results accurately and within established timelines * Operate ...
$46K - $96K/yr
We are seeking Scientist, Method Validation to join IQVIA Laboratories at Ithaca, NY. We hire ... Analyze laboratory data and report results accurately and within established timelines * Operate ...
$46K - $96K/yr
We are seeking Scientist, Method Validation to join IQVIA Laboratories at Ithaca, NY. We hire ... Analyze laboratory data and report results accurately and within established timelines * Operate ...
$46K - $96K/yr
We are seeking Scientist, Method Validation to join IQVIA Laboratories at Ithaca, NY. We hire ... Analyze laboratory data and report results accurately and within established timelines * Operate ...
Author method validation protocols and reports in full compliance with ICH Q2(R2), USP , and applicable regulatory guidance for late-phase and commercial programs. * Lead analytical method ...
Author method validation protocols and reports in full compliance with ICH Q2(R2), USP , and applicable regulatory guidance for late-phase and commercial programs. * Lead analytical method ...
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 ...
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 ...
$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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
Quick apply
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 ...
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 ...
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 ...
Quick apply
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 ...
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 ...
Waunakee, WI · On-site
The SA Chemist is responsible for analytical method development, method validation and performing chemical testing and analyses in accordance with written procedures. This work is conducted in ...
Waunakee, WI · On-site
The SA Chemist is responsible for analytical method development, method validation and performing chemical testing and analyses in accordance with written procedures. This work is conducted in ...
Waunakee, WI · On-site
The SA Chemist is responsible for analytical method development, method validation and performing chemical testing and analyses in accordance with written procedures. This work is conducted in ...
Waunakee, WI · On-site
The SA Chemist is responsible for analytical method development, method validation and performing chemical testing and analyses in accordance with written procedures. This work is conducted in ...
$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.
Cities with the most Analytical Method Validation job openings:
States with the most job openings for Analytical Method Validation jobs include:
The top searched job categories for Analytical Method Validation jobs are:

8.1
Based on 53 frontline employees who took The Breakroom Quiz
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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $46,200.00 - $96,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.Sourced by ZipRecruiter
At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.
Health care and social assistance
10,000+ Employees
Durham, NC, US