We are seeking Scientists (LCMS-MS Bioanalysis & Method Validation) to join IQVIA Laboratories at Ithaca, NY. We hire passionate innovators who drive healthcare forward through thoughtful and ...
We are seeking Scientists (LCMS-MS Bioanalysis & Method Validation) to join IQVIA Laboratories at Ithaca, NY. We hire passionate innovators who drive healthcare forward through thoughtful and ...
Analytical Method Development & Validation * Oversee development, qualification, transfer, and ICH-compliant validation of analytical methods. * Ensure assays meet regulatory expectations for ...
Analytical Method Development & Validation * Oversee development, qualification, transfer, and ICH-compliant validation of analytical methods. * Ensure assays meet regulatory expectations for ...
Technical Writer II / Method Validation documents / Remote work Duration: 12 months contract, extendable up to 48 months Location: Remote Worker Note: The client has the right-to-hire you as a ...
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Technical Writer II / Method Validation documents / Remote work Duration: 12 months contract, extendable up to 48 months Location: Remote Worker Note: The client has the right-to-hire you as a ...
Analytical Method Development & Validation * Oversee development, qualification, transfer, and ICH-compliant validation of analytical methods. * Ensure assays meet regulatory expectations for ...
Analytical Method Development & Validation * Oversee development, qualification, transfer, and ICH-compliant validation of analytical methods. * Ensure assays meet regulatory expectations for ...
Validation Engineer
Cambridge, MA · On-site
Candidates must have strong hands-on expertise in IQ/OQ/PQ protocol development and execution for both new and legacy manufacturing processes and equipment, as well as Test Method Validation (TMV ...
New
Validation Engineer
Cambridge, MA · On-site
Candidates must have strong hands-on expertise in IQ/OQ/PQ protocol development and execution for both new and legacy manufacturing processes and equipment, as well as Test Method Validation (TMV ...
New
QC Senior/Principal Scientist, Analytical Method Validation
Lexington, MA · On-site
$120K - $160K/yr
JOB SUMMARY The QC Senior/Principal Scientist for Analytical Method Validation is key role within our Quality Control Technical Services (QCTS) department within our CDMO facility. The individual in ...
QC Senior/Principal Scientist, Analytical Method Validation
Lexington, MA · On-site
$120K - $160K/yr
JOB SUMMARY The QC Senior/Principal Scientist for Analytical Method Validation is key role within our Quality Control Technical Services (QCTS) department within our CDMO facility. The individual in ...
Senior Engineer - Test Method Validation
North Andover, MA · On-site
$95 - $100/hr
Job Overview: Pay Range: $95hr - $100hr Requirement/Must Have: * Quality background preferred. * Exceptional analytical and technical writing skills. * Bachelor's degree in Engineering. * Ability to ...
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Senior Engineer - Test Method Validation
North Andover, MA · On-site
$95 - $100/hr
Job Overview: Pay Range: $95hr - $100hr Requirement/Must Have: * Quality background preferred. * Exceptional analytical and technical writing skills. * Bachelor's degree in Engineering. * Ability to ...
Responsibilities include analytical method optimization, method validation, comparability assessments, and the evaluation of new technologies. The role requires a solid understanding of scientific ...
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Responsibilities include analytical method optimization, method validation, comparability assessments, and the evaluation of new technologies. The role requires a solid understanding of scientific ...
Validation Engineer
Manchester, NH · On-site
Candidates must have strong hands-on expertise in IQ/OQ/PQ protocol development and execution for both new and legacy manufacturing processes and equipment, as well as Test Method Validation (TMV ...
New
Validation Engineer
Manchester, NH · On-site
Candidates must have strong hands-on expertise in IQ/OQ/PQ protocol development and execution for both new and legacy manufacturing processes and equipment, as well as Test Method Validation (TMV ...
New
JOB SUMMARY The QC Senior/Principal Scientist for Analytical Method Validation is key role within our Quality Control Technical Services (QCTS) department within our CDMO facility. The individual in ...
JOB SUMMARY The QC Senior/Principal Scientist for Analytical Method Validation is key role within our Quality Control Technical Services (QCTS) department within our CDMO facility. The individual in ...
Senior Engineer - Test Method Validation
North Andover, MA · On-site
$95 - $100/hr
Job Overview: Pay Range: $95hr - $100hr Requirement/Must Have: Quality background preferred. Exceptional analytical and technical writing skills. Bachelor's degree in Engineering. Ability to work in ...
Senior Engineer - Test Method Validation
North Andover, MA · On-site
$95 - $100/hr
Job Overview: Pay Range: $95hr - $100hr Requirement/Must Have: Quality background preferred. Exceptional analytical and technical writing skills. Bachelor's degree in Engineering. Ability to work in ...
JOB SUMMARY The QC Senior/Principal Scientist for Analytical Method Validation is key role within our Quality Control Technical Services (QCTS) department within our CDMO facility. The individual in ...
Quick apply
JOB SUMMARY The QC Senior/Principal Scientist for Analytical Method Validation is key role within our Quality Control Technical Services (QCTS) department within our CDMO facility. The individual in ...
Eurofins Small Molecule Method Establishment is seeking a Senior Scientist to perform method validations, method transfers, and method verification activities on APIs and finished products. The team ...
Eurofins Small Molecule Method Establishment is seeking a Senior Scientist to perform method validations, method transfers, and method verification activities on APIs and finished products. The team ...
Eurofins Small Molecule Method Establishment is seeking a Senior Scientist to perform method validations, method transfers, and method verification activities on APIs and finished products. The team ...
Eurofins Small Molecule Method Establishment is seeking a Senior Scientist to perform method validations, method transfers, and method verification activities on APIs and finished products. The team ...
Eurofins Small Molecule Method Establishment is seeking a Senior Scientist to perform method validations, method transfers, and method verification activities on APIs and finished products. The team ...
Quick apply
Eurofins Small Molecule Method Establishment is seeking a Senior Scientist to perform method validations, method transfers, and method verification activities on APIs and finished products. The team ...
Senior Engineer - Test Method Validation
North Andover, MA · On-site
$95 - $100/hr
Job Overview: Pay Range: $95hr - $100hr Requirement/Must Have: * Quality background preferred. * Exceptional analytical and technical writing skills. * Bachelor's degree in Engineering. * Ability to ...
Quick apply
Senior Engineer - Test Method Validation
North Andover, MA · On-site
$95 - $100/hr
Job Overview: Pay Range: $95hr - $100hr Requirement/Must Have: * Quality background preferred. * Exceptional analytical and technical writing skills. * Bachelor's degree in Engineering. * Ability to ...
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 ...
Develop and validate test methods for complex electromechanical medical device systems to verify essential clinical and system performance requirements. Demonstrate expertise in converting design and ...
Develop and validate test methods for complex electromechanical medical device systems to verify essential clinical and system performance requirements. Demonstrate expertise in converting design and ...
Strong hands-on experience with microbiological method validation , including protocol development, execution, documentation, and comparative testing in a cGMP-regulated environment . * Experience ...
Strong hands-on experience with microbiological method validation , including protocol development, execution, documentation, and comparative testing in a cGMP-regulated environment . * Experience ...
Perform detailed assessments to identify remediation scope across Operational Qualification (OQ), Performance Qualification (PQ), Test Method Validation (TMV), and In-Process Monitoring (IPM)
Perform detailed assessments to identify remediation scope across Operational Qualification (OQ), Performance Qualification (PQ), Test Method Validation (TMV), and In-Process Monitoring (IPM)
Method Validation information
See salary details
$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
How much do method validation jobs pay per hour?
What are the key skills and qualifications needed for method validation?
To excel in Method Validation, a strong background in analytical chemistry, laboratory techniques, and scientific data analysis is typically required, often supported by a degree in chemistry, biochemistry, or a related field. Familiarity with validation protocols, industry regulations (such as GLP, GMP, or ISO standards), and analytical instrumentation (e.g., HPLC, GC, MS) is essential. Strong attention to detail, problem-solving skills, and effective collaboration and documentation abilities help professionals thrive in this position. These skills are vital to ensure that laboratory methods are reliable, regulatory-compliant, and suitable for their intended purposes.
What is a method validation?
A Method Validation job involves assessing and verifying analytical methods to ensure they produce reliable, accurate, and reproducible results. Professionals in this role typically work in pharmaceutical, biotechnology, or chemical industries, following regulatory guidelines such as ICH, USP, or FDA requirements. Their responsibilities include designing validation protocols, performing experiments, analyzing data, and documenting results. Method validation ensures compliance with industry standards and guarantees product quality and safety.
What does a method validation do?
As a Method Validation professional, you will design, conduct, and document experiments to confirm that laboratory methods produce accurate and reproducible results under specified conditions. Typical daily tasks include preparing protocols, running validation samples, analyzing data, and preparing comprehensive validation reports for internal or regulatory review. You’ll work closely with scientists, quality assurance teams, and regulatory specialists to ensure compliance with industry standards. This collaborative environment provides opportunities to contribute to critical product development stages and to build expertise that supports career progression into quality management, regulatory affairs, or advanced analytical roles.
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 Method Validation jobs?
States with the most job openings for Method Validation jobs include:
What job categories do people searching Method Validation jobs look for?
The top searched job categories for Method Validation jobs are:

$46K - $108K/yr
Full-time
Medical, Life
Re-posted 26 days ago
IQVIA rating
8.1
Based on 53 frontline employees who took The Breakroom Quiz
62nd of 224 rated it services
Job description
We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.
IQVIA Laboratories in Ithaca, NY has multiple Scientist opportunities open across LC-MS bioanalysis and method validation teams. Apply to this posting if you're interested in Scientist roles focused on generating high-quality data for both large and small molecule workflows in a regulated laboratory environment.
What You'll Be Doing:
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Follow all applicable health, safety, and regulatory standards while performing laboratory work
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Design, set up, and execute qualitative and quantitative experiments to support LC-MS bioanalysis, method validation, and downstream sample analysis
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Prepare, extract, and process samples using techniques such as protein precipitation, solid-phase extraction, and immunocapture as applicable to the assay
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Operate, calibrate, tune, and optimize LC-MS instrumentation (including Triple Quadrupole mass spectrometers and UPLC systems) and perform routine maintenance and troubleshooting per SOPs
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Review, interpret, integrate, and summarize chromatographic and mass spectrometry data; identify data abnormalities and initiate appropriate troubleshooting studies using sound scientific judgment
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Prepare documentation and deliverables including protocols, technical summaries and reports, GLP-compliant laboratory notebook entries, and data packages for project outcomes
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Collaborate with Project Management and cross-functional stakeholders to plan work, communicate progress, and meet study objectives within tight timelines
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Contribute to continuous improvement by helping evaluate new technologies and techniques and supporting process improvements within the lab
What We Are Looking For:
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Bachelor's Degree in applied/laboratory sciences or a relevant scientific discipline with direct laboratory coursework
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Hands-on experience with LC-MS workflows including operation of Triple Quadrupole and/or high resolution mass spectrometers, UPLC systems, calibration and tuning, and data interpretation.
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Knowledge of sample handling and preparation techniques (e.g., protein precipitation, SPE, immunocapture) and familiarity with GLP documentation standards; experience preparing data for LIMS (e.g., Watson) is a plus
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Other Equivalent combination of education, training, and experience may be accepted in lieu of degree
The Knowledge, Skills and Abilities Needed for This Role:
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Strong attention to detail and commitment to producing high-quality, compliant data and documentation to timelines
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Ability to troubleshoot complex experiments and laboratory equipment, clearly present findings, and know what to escalate versus address independently
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Effective communication and interpersonal skills in a collaborative team environment, including working with project teams and cross-functional stakeholders
What We Offer You:
We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.
To learn more about our benefits, visit https://jobs.iqvia.com/benefits.
If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!
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 - $108,000.00. 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.About IQVIA
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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.
Industry
Health care and social assistance
Company size
10,000+ Employees
Headquarters location
Durham, NC, US