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Method Development Jobs in Illinois (NOW HIRING)

Sr Scientist

Melrose Park, IL ยท On-site

$95 - $110/hr

The ability to apply chemistry knowledge for problem-solving and innovative approaches in Method development, Method Validation, and analytical testing is required.* Prior knowledge and work ...

New

QC REVIEW SPECIALIST II

Bloomingdale, IL ยท On-site

$35.54 - $40/hr

Coordinates with Method Development and/or Lab Management for resolution of any deviations from methods, discrepancies with specifications. * Reviews data and reports associated with method transfers ...

Senior QC Analyst

Wheeling, IL ยท On-site

$25 - $33/hr

Method development -- Develop, validate, and document analytical methods for new sample types and product formats. * Documentation and compliance -- Maintain laboratory documentation in alignment ...

Showing results 41-60

Method Development information

See Illinois salary details

$28.1K

$51.8K

$78.5K

How much do method development jobs pay per year?

As of Aug 20, 2026, the average yearly pay for method development in Illinois is $51,763.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,200.00 and $58,100.00 per year, depending on experience, location, and employer.

What is method development?

Method development refers to the process of creating, optimizing, and validating analytical procedures or techniques used to identify, quantify, and analyze substances in various samples. This is crucial in industries like pharmaceuticals, environmental testing, and food safety to ensure accurate and reliable results. The process involves selecting appropriate instruments, developing sample preparation steps, and validating the method to meet regulatory and quality standards. Skilled professionals in method development help ensure that tests are robust, reproducible, and suitable for their intended purposes.

What are the key skills and qualifications needed to thrive in method development?

To excel in Method Development, you need a strong background in analytical chemistry, laboratory techniques, and scientific problem-solving, often supported by a degree in chemistry or a related field. Familiarity with analytical instruments such as HPLC, GC, and mass spectrometry, as well as knowledge of relevant regulatory guidelines and software for data analysis, is typically required. Attention to detail, critical thinking, and effective communication are crucial soft skills for designing robust methods and collaborating with cross-functional teams. These capabilities ensure the development of accurate, reliable methods that support research, quality control, and regulatory compliance.

What are some common challenges encountered in a method development role, and how are they typically addressed?

Professionals in Method Development often face challenges such as optimizing analytical techniques for complex samples, ensuring methods are robust and reproducible, and meeting stringent regulatory requirements. Addressing these challenges involves a systematic approach, including thorough literature review, iterative experimentation, and close collaboration with cross-functional teams (such as Quality Assurance and R&D) to validate and troubleshoot methods. Staying updated on industry best practices and regulatory guidelines is also crucial for success in this role.

What is the difference between Method Development vs Analytical Chemist?

AspectMethod DevelopmentAnalytical Chemist
Primary FocusDesigning and optimizing new analytical methodsPerforming analysis using established methods
Work EnvironmentResearch labs, R&D departmentsQuality control labs, manufacturing facilities
Required CredentialsBachelor's or higher in Chemistry or related field; experience in method developmentBachelor's or higher in Chemistry; experience in analytical techniques

Method Development specialists focus on creating and refining new analytical procedures, while Analytical Chemists primarily perform routine analysis using existing methods. Both roles require strong chemistry knowledge, but Method Development involves more innovation and method optimization, often in research settings, whereas Analytical Chemists focus on quality control and routine testing in production environments.

Infographic showing various Method Development job openings in Illinois as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 11% Part Time, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $51,763 per year, or $24.9 per hour.

Principal Scientist I, Biologics Analytical R&D (External Programs)

Allergan

North Chicago, IL โ€ข On-site

$150 - $230/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 13 days ago


Job description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow AbbVie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description Overview

AbbVie Biologics Analytical Research & Development (Biologics ARD) is a global analytical sciences organization responsible for CMC analytical activities related to the development of AbbVie's therapeutic biologic products. Our scope includes AbbVie's diverse pipeline of innovative therapeutic biologics medicines, including monoclonal antibodies, antibody drug conjugates (ADC), and other novel modalities, and spans from the selection of Discovery candidate molecules through the transition of analytical methods and testing to operations partners for late stage development. We are building a worldโ€‘class team of scientists and leaders who will drive the advancement of industryโ€‘leading analytical capabilities and make meaningful contributions to advance AbbVie's pipeline of innovative medicines. Careers in AbbVie Biologics ARD provide unique opportunities to work with global and crossโ€‘functional teams to drive exceptional science and innovative product development strategies.

The Analytical Development โ€“ External Programs group within Biologics ARD is responsible for early development (through clinical proof of concept) of programs with outsourced analytical activities. The candidate will serve as analytical lead on internal CMC teams and will work with external parties on method development, optimization, validation/transfer, and testing of clinical supplies to meet analytical deliverables for their given development programs. In collaboration with crossโ€‘functional partners, the lead will define analytical strategies for formulation and process development studies. Key deliverables include robust analytical methods, clinical supplies release testing and stability studies to establish clinical product dating, product control strategies informed by analytical data and method understanding, comprehensive data packages that drive product and process understanding, and regulatory submission content.

Major Responsibilities
  • As analytical lead, develop analytical strategies and communicate to Analytical R&D functions and CMC business partners for experimental execution in support of stability studies, product analytical control strategies, comparability studies and extended characterization of biologics.
  • Collaborate with third party laboratories to ensure CMC timelines are met.
  • Interpret and identify data trends in key analytical release and stability assays.
  • Author and/or review key regulatory documents, laboratory data, technical memos and reports.
  • Proactively advise and share knowledge/expert opinions with peers and senior management. Mentor peers in project management and development of analytical strategies.
  • Demonstrate scientific excellence in analytical characterization of biologics internally and externally and build and foster an active network of consortia collaborations.
  • Brainstorm ideas for continuous improvement activities and lead/participate in initiatives.
  • Understand and adhere to corporate standards regarding code of conduct, safety, and GXP compliance.
Qualifications
  • MS (12+ years), or PhD (6+ years) in Chemistry, Biochemistry, or Biology with previous work experience (6+ years) in a pharmaceutical laboratory setting.
  • Preferred candidate should have experience in project management/leadership of analytical development activities for biologic compounds (mAbs, antibody drug conjugates and/or fusion proteins).
  • Experience and strong knowledge of protein HPLC (e.g., SEC, IEX, HIC), capillary electrophoresis, and other separation techniques as applied to protein analysis.
  • Demonstrated scientific writing skills and excellent verbal communication skills.
  • Experience in laboratory systems (LIMS, CDS, ELN) preferred.
  • Statistical knowledge and experience are preferred, e.g. capability analysis, gauge R&R and design of experiments (DOE) methodologies.
Key AbbVie Competencies
  • Interact well with diverse groups within function and maintain strong working relationships with internal and external collaborators to enable higher performance.
  • Learns fast, grasps the โ€œessenceโ€ and can change course quickly where indicated.
  • Raises the bar and is never satisfied with the status quo.
  • Creates a learning environment, open to suggestions and experimentation for improvement.
  • Embraces the ideas of others, nurtures innovation and manages innovation to reality.

Level and compensation will be commensurate with experience.

Additional Information
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our longโ€‘term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Companyโ€™s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

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