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Method Development Chemist Jobs (NOW HIRING)

Abbott

Method Development Scientist

Santa Rosa, CA · On-site

$90K - $180K/yr

D. in Analytical Chemistry or related discipline with 1 year of commercial toxicology laboratory experience. * At least 6 months hands-on experience in LC-MS/MS method development and validation for ...

FLEXSYS

Process Development Chemist

Akron, OH · On-site

Apply Design of Experiments (DoE) and data-driven methods to optimize process performance ... process development and manufacturing. ? Strong understanding of reaction chemistry, unit ...

Abbott

Method Development Scientist

Santa Rosa, CA

$90K - $180K/yr

D. in Analytical Chemistry or related discipline with 1 year of commercial toxicology laboratory experience. * At least 6 months hands-on experience in LC-MS/MS method development and validation for ...

Qnity

Associate R&D Chemist

Marlborough, MA · On-site

$25.25 - $33.25/hr

Associate R&D Chemist (contract) Location: Marlborough, MA Company: Qnity Electronics Inc. Business ... Conduct routine and non-routine material characterization using methods such as GPC / SEC, HPLC ...

New

Lancesoft INC

Chemist

Northridge, CA · On-site

$40 - $42/hr

Responsibilities also include assisting in method development, maintaining laboratory instrumentation, and ensuring compliance with * laboratory protocols. * The Chemist II will contribute to ...

New

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Method Development Chemist information

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$91K

How much do method development chemist jobs pay per year?

As of Sep 2, 2026, the average yearly pay for method development chemist in the United States is $71,500.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,000.00 and $79,000.00 per year, depending on experience, location, and employer.

What does a method development chemist do?

A Method Development Chemist is responsible for designing, developing, and validating analytical methods to accurately measure chemical compounds in various samples. They work primarily in laboratories, often within the pharmaceutical, environmental, or food industries, to ensure that testing methods are reliable, reproducible, and compliant with regulatory standards. Their work is critical for quality control, product development, and ensuring the safety and efficacy of products. Method Development Chemists also troubleshoot and optimize existing methods to improve accuracy or efficiency.

What are some common challenges faced by method development chemists when transferring analytical methods to a production environment?

Method Development Chemists often encounter challenges when transferring analytical methods from the laboratory to production settings, such as variations in equipment, differences in sample matrices, and scalability issues. Ensuring method robustness and reproducibility across different instruments or sites is critical, requiring thorough validation and clear documentation. Collaborating closely with production teams and quality assurance professionals helps address these challenges, ensuring a smooth transition and consistent results in large-scale operations.

What are the key skills and qualifications needed to thrive as a method development chemist, and why are they important?

To thrive as a Method Development Chemist, you need a solid background in analytical chemistry, method validation, and experience with laboratory instrumentation, usually supported by a degree in chemistry or a related field. Proficiency in techniques such as HPLC, GC, LC-MS, and familiarity with regulatory guidelines (e.g., ICH, FDA) and laboratory information management systems (LIMS) is typically required. Strong problem-solving abilities, attention to detail, and effective communication skills help you excel in collaborating with cross-functional teams and troubleshooting complex analytical issues. These skills and qualifications are vital to ensure reliable, accurate results and to maintain compliance with industry standards in method development projects.

What is the difference between Method Development Chemist vs Analytical Chemist?

AspectMethod Development ChemistAnalytical Chemist
Primary FocusDeveloping and optimizing new analytical methodsPerforming routine analysis and testing samples
Work EnvironmentResearch labs, R&D departmentsQuality control labs, manufacturing settings
Required CredentialsBachelor's or Master's in Chemistry or related fieldBachelor's or Master's in Chemistry or related field
Industry UsagePharmaceuticals, biotech, chemical manufacturingPharmaceuticals, food, environmental testing

While both roles require a strong chemistry background and similar educational credentials, a Method Development Chemist primarily focuses on creating and refining new analytical techniques, whereas an Analytical Chemist performs routine testing and analysis to ensure product quality. The roles often overlap but differ in scope and daily responsibilities.

How to become a method development chemist?

To become a method development chemist, typically a bachelor's degree in chemistry, biochemistry, or a related field is required, with many roles preferring a master's or Ph.D. for advanced positions. Relevant skills include knowledge of analytical techniques such as HPLC, GC, and spectroscopy, along with experience in method validation and troubleshooting. Gaining hands-on experience through internships or laboratory work and obtaining certifications like ASQ's Certified Quality Improvement Associate can enhance prospects.

What is method development in chemistry?

Method development in chemistry involves creating and optimizing analytical procedures to accurately detect, quantify, and analyze specific compounds or substances. For a Method Development Chemist, this includes selecting appropriate techniques, validating methods, and ensuring reproducibility using tools like chromatography or spectroscopy within a regulated environment.
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Method Development Chemist jobs near you
Infographic showing various Method Development Chemist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $71,500 per year, or $34.4 per hour.

Method Development Scientist

Abbott

Santa Rosa, CA • On-site

$90K - $180K/yr

Full-time

Medical, Life, Retirement

Re-posted 25 days ago

Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

169th of 545 rated manufacturers

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.
JOB DESCRIPTION:
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:
  • Career development with an international company where you can grow the career you dream of.
  • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
  • An excellent retirement savings plan with a high employer contribution.
  • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.
  • A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
  • A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity
This position works out of our Santa Rosa, CA location in the Toxicology Business Unit in Rapid Diagnostics at Abbott. This role is on site daily.
The person hired in this role will be developing LC-MS-MS methods for the determination of drugs and metabolites in urine and oral fluid specimens. This role will also be instrumental in providing new testing options and accurate and timely test results to our clients.
What You'll Work On
  • Perform method development for new and existing assays
  • Transfer method to method validations team
  • Troubleshoot existing analytical methods
  • Author, review, and verify validation protocols and reports
  • Support production team with high-throughput analytical testing.
  • Anticipate, recognize, and resolve complex technical issues through job knowledge, use of technical resources and well formulated, logical experimentation
  • Advance the technical capabilities of the department by evaluating, recommending and implementing new technologies to meet business needs.
  • Author quality and regulatory test method documents.
  • Manage analytical projects
  • Present project results and recommendations to senior management
  • Provide guidance (scientific and administrative) for junior analytical scientists
  • Proactively and cooperatively communicate with peers and management to ensure awareness of progress and issues; recommend solutions when issues arise
  • Follow, understand and comply with SOP's and policies on GLP's and safety.

Required Qualifications
  • Bachelor's Degree from an accredited college or university in chemistry, biochemistry or related discipline.
  • 6 years of similar work experience
  • Wide application of technical principles, practices, and procedures.
    Strong understanding of business unit function and cross group dependencies/relationships.
  • Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations.
  • Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors.
  • Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.
  • Has a sound knowledge of various technical alternatives and their impact.
  • Related work experience with a strong understanding of specified functional area.

Preferred Qualifications
  • Ph.D. in Analytical Chemistry or related discipline with 1 year of commercial toxicology laboratory experience.
  • At least 6 months hands-on experience in LC-MS/MS method development and validation for pharmaceuticals in biological specimens
  • Recent experience with Sciex (Analyst, Multiquant, Sciex OS) software and instrumentation.
  • Recent experience in method validation of forensic toxicology techniques in accordance to published ANSI/ASB 036 or other published forensic toxicology standards.
  • Experience with Hamilton Nimbus/STAR automation platforms
  • 2 or more years of LC-MS/MS hands-on experience in LC-MS/MS method development and validation for pharmaceuticals in biological specimens.

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: https://abbottbenefits.com/
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at abbott.com, on LinkedIn at https://www.linkedin.com/company/abbott-/, and on Facebook at https://www.facebook.com/AbbottCareers.
The base pay for this position is
$90,000.00 - $180,000.00
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Research and Discovery
DIVISION:
TOX ARDx Toxicology
LOCATION:
United States > Santa Rosa : 3700-3730 Westwind Blvd.
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes, 5 % of the Time
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Lift, carry, push or pull weights of more than 20 pounds/9 kilos on a regular/daily basis, Routine work with chemicals, Work with human blood or other potentially infectious materials, Work with infectious organisms or known infectious materials
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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