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Analytical Method Validation Jobs in Darien, IL (NOW HIRING)

Frontage Laboratories

Analytical Chemist

Chicago, IL · On-site

$65K - $80K/yr

This position involves formulating, developing and validating methodologies for dose formulation analysis. As needed, the Analytical Chemist supervises support personnel and reports to the Director ...

Fresenius Kabi

Scientist

Melrose Park, IL · On-site

$70 - $75/hr

Plans, develops, and implements scientifically well-designed experimental programs and demonstrates creativity and capability in analytical method development, validation, and testing.Identifies ...

F.tech Inc.

Engineer, Validation

Chicago, IL · On-site

$70 - $95/hr

Evaluate validation requirements from automotive clients and develop adequate test methods and ... Create and maintain engineering validation and analysis reports like ADVPR and communicate with ...

Fresenius Kabi USA, LLC

Validation Engineer

Melrose Park, IL · On-site

$65K - $80K/yr

Executes validation studies (utility, equipment, cleaning, process, computer, and new products) to ... Understanding of statistical analysis tools and methods. * Knowledge of cGMP room classifications ...

New

Fresenius Kabi

Validation Engineer

Melrose Park, IL · On-site

$65K - $80K/yr

Executes validation studies (utility, equipment, cleaning, process, computer, and new products) to ... Understanding of statistical analysis tools and methods. * Knowledge of cGMP room classifications ...

Freseniusglobal

Validation Engineer

Melrose Park, IL · On-site

$65K - $80K/yr

Executes validation studies (utility, equipment, cleaning, process, computer, and new products) to ... Understanding of statistical analysis tools and methods. * Knowledge of cGMP room classifications ...

Ace Technologies, Inc.

Validation Engineer

Chicago, IL · On-site

... validation, process improvement, testing, and inspection to ensure that products are ideal and ... Applies statistical process control (SPC) methods for analyzing data to evaluate the current ...

Fresenius Kabi

Validation Engineer

Melrose Park, IL · On-site

$65K - $80K/yr

Executes validation studies (utility, equipment, cleaning, process, computer, and new products) to ... Understanding of statistical analysis tools and methods. * Knowledge of cGMP room classifications ...

Fresenius Kabi USA, LLC

Validation Engineer

Melrose Park, IL · On-site

$65K - $80K/yr

Executes validation studies (utility, equipment, cleaning, process, computer, and new products) to ... Understanding of statistical analysis tools and methods. * Knowledge of cGMP room classifications ...

New

Freseniusglobal

Validation Engineer

Melrose Park, IL · On-site

$65K - $80K/yr

Executes validation studies (utility, equipment, cleaning, process, computer, and new products) to ... Understanding of statistical analysis tools and methods. * Knowledge of cGMP room classifications ...

Deloitte

Model Validation Consultant

Chicago, IL · On-site

Evaluate model performance and stability using appropriate methods such as benchmarking, back ... error analysis, and scenario-based evaluation. * Support validation of GenAI and Agentic AI ...

Alliant Credit Union

Lead Model Validation

Chicago, IL · Hybrid

$95K - $163K/yr

Apply sound analytical judgment to evaluate model input data, conceptual soundness, performance ... Support the ongoing enhancement of model validation methods, tools, templates, and practices in ...

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All JobsAnalytical Method Validation JobsAnalytical Method Validation Jobs in Darien, IL

Analytical Method Validation information

See Darien, IL salary details

$22

$50

$76

How much do analytical method validation jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for analytical method validation in Darien, IL is $50.64, according to ZipRecruiter salary data. Most workers in this role earn between $38.41 and $61.59 per hour, depending on experience, location, and employer.

What is an analytical method validation?

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.

What does a typical day look like for someone working in analytical method validation?

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.

What are the key skills and qualifications needed to thrive in analytical method validation, and why are they important?

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.

Analytical Method Validation jobs near you
Infographic showing various Analytical Method Validation job openings in Darien, IL as of August 2026, with employment types broken down into 91% Full Time, 7% Part Time, and 2% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $105,332 per year, or $50.6 per hour.

Analytical Chemist &ndash

Noblesoft Technologies

Des Plaines, IL • On-site

Contractor

Re-posted 15 days ago

Job description

Job Title: Analytical Chemist – Ion Chromatography & HPLC
Location: Des Plaines, Illinois
 

Key Responsibilities:
  • Develop and validate IC and HPLC methods for the characterization of raw materials, buffers, and critical reagents used in IVD assays.
  • Support reagent and assay development teams by providing analytical data to guide formulation, stability, and performance optimization.
  • Operate, maintain, and troubleshoot analytical instrumentation, including IC and HPLC systems with various detectors (e.g., UV, conductivity, MS).
  • Design and execute method robustness and transfer studies to support product development,  tech transfer, lifecycle management, and regulatory submissions
  • Generate and review technical documentation, including protocols, validation reports, and SOPs, in compliance with IVD regulatory standards (e.g., FDA, ISO 13485, CLSI).
  • Collaborate with R&D, Quality, and Manufacturing teams to support product development, process validation, and root cause investigations.
  • Interpret complex analytical data and generate technical reports, protocols, and SOPs in
  • Ensure compliance with regulatory guidelines (FDA, ICH, USP, etc.) and internal quality systems.
  • Train and mentor junior staff in analytical techniques and instrumentation best practices.
 
 
Qualifications:
  • Bachelor’s, Master’s, or Ph.D. in Analytical Chemistry, Chemistry, Biochemistry, or a related field.
  • 5+ years of hands-on experience in IC and HPLC method development, preferably in the IVD, medical device, or pharmaceutical industry.
  • Strong understanding of analytical method validation in a regulated environment (FDA, ISO 13485, ICH).
  • Proficiency with analytical software (e.g., Chromeleon, Empower, ChemStation) and data integrity principles.
  • Familiarity with IVD assay components, such as enzymes, antibodies, and buffers, is highly desirable.
  • Excellent documentation, communication, and problem-solving skills.
 
 
Preferred Skills:
  • Experience with biologics, enzymes, or complex matrices.
  • Familiarity with other analytical techniques such as GC, CE, or spectroscopy.
  • Knowledge of data integrity principles and electronic laboratory systems (e.g., LIMS, ELN).
  • Knowledge of design control and risk management in the context of IVD product development.
  • Prior experience supporting 510(k) or PMA submissions is a plus