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Method Development Chemist Jobs in Phoenix, AZ (NOW HIRING)

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We are seeking a Method Development and Validation Chemist I to help validate, optimize, and support these analytical methods that power our client testing services. If you are a driven analytical ...

The Role The Metrology R&D Chemist will develop and implement new advanced QC metrologies and ... Employee is responsible for developing statistically and technically sound analytical test methods ...

The Role The Metrology R&D Chemist will develop and implement new advanced QC metrologies and ... Employee is responsible for developing statistically and technically sound analytical test methods ...

The Role The Metrology R&D Chemist will develop and implement new advanced QC metrologies and ... Employee is responsible for developing statistically and technically sound analytical test methods ...

Method and test plan development * Leading various characterization and design projects * Following ... ACS certified Chemistry degree with strong analytical/instrumentation skills * Understanding of ...

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Method Development Chemist information

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$43.7K

$71K

$90.4K

How much do method development chemist jobs pay per year?

As of Aug 11, 2026, the average yearly pay for method development chemist in Phoenix, AZ is $70,993.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,500.00 and $78,400.00 per year, depending on experience, location, and employer.

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 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 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.

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 popular job titles related to Method Development Chemist jobs in Phoenix, AZ? For Method Development Chemist jobs in Phoenix, AZ, the most frequently searched job titles are:
What job categories do people searching Method Development Chemist jobs in Phoenix, AZ look for? The top searched job categories for Method Development Chemist jobs in Phoenix, AZ are:
Infographic showing various Method Development Chemist job openings in Phoenix, AZ as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $70,993 per year, or $34.1 per hour.

Chemist - Method Development and Validation

Omnient Labs

Tempe, AZ • On-site

$60K - $70K/yr

Full-time

Posted 4 days ago

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Job description

Omnient Labs is a growing contract testing laboratory in the dietary supplement and botanical space, based in Tempe, AZ. We work on novel formulations and emerging bioactives, developing and validating methods that do not yet exist in compendia. We are seeking a Method Development and Validation Chemist I to help validate, optimize, and support these analytical methods that power our client testing services. If you are a driven analytical chemist who thrives on new challenges in a fast‐paced, collaborative lab, we look forward to speaking with you. Apply today.

This position is in-person/on site. This is not a remote position. Must reside in the Phoenix Metro Valley.

Job Type: Full-time, Monday through Friday, Day Shift

Salary: 60 - 70k/yr

Omnient Labs offers a benefits package which includes Medical, Dental, Vision, matching 401(k), employee discounts, PTO and more.

Pre-employment background check mandatory.

Chemist – Method Development and Validation Duties:

  • Perform method validation, verification, and robustness studies for established HPLC, UPLC, LC‐MS/MS, HS‐GC, GC‐FID, HPTLC, UV‐Vis, and FTIR methods under the direction of senior method development staff.
  • Assist with development of lower‐complexity analytical methods for routine testing, following USP <1225>, USP <1226>, and AOAC Appendix K, with technical review by senior chemists.
  • Support method transfer activities (e.g., HPLC to UPLC) for routine methods, including preparation of associated documentation and data packages.
  • Perform method optimization for already developed methods (such as minor adjustments to gradients, injection volumes, sample preparation steps) to improve robustness and efficiency.
  • Train quality control chemists on validated and transferred methods and provide routine technical support, escalating complex issues to senior chemists.
  • Execute non‐routine testing of Research and Development (R&D) materials using established methods and summarize results for senior review.
  • Analyze samples to determine chemical and/or physical properties, composition, and/or structure utilizing chromatography, spectroscopy, and spectrophotometry according to approved methods.
  • Maintain a well‐documented laboratory notebook and ensure all work complies with cGLP and cGMP guidelines.
  • Participate in daily laboratory functions, calibration activities, hygiene events, and routine laboratory cleaning and maintenance.
  • Assist with writing and editing laboratory documentation such as standard operating procedures, test methods, or training protocols under direction of laboratory management.
  • Perform chemical and physical inventory of laboratory supplies, reagents, solvents, and standards on a consistent basis.
  • Support instrumentation calibration and maintenance schedules to ensure proper condition and calibration of laboratory instrumentation and equipment.
  • File appropriate paperwork when modifications to laboratory procedures or processes are necessary, such as deviations and change control documentation, with input from senior staff.
  • Other miscellaneous duties as assigned by laboratory management.

Education/Experience:

A bachelor’s degree in chemistry or chemistry related field, such as biochemistry or molecular biology, is required. A bachelor’s degree in a hard-scientific field such as physics or biology is acceptable. At least 1 year of method development experience (or equivalent) in the food or dietary supplements industry is required.

Technical Skills:

Digital

  • Proficient using Waters Empower 3 software
  • Proficient in web-based applications

Analytical

  • Proficiency with analytical instrumentation such as, HPLC/UPLC, LCMS, specifically Waters UPLC’s
  • Strong analytical technique and instrumentation skills
  • Familiar and/or proficient with simple mathematical manipulations and algebra
  • Meticulous attention to detail, dependability, and excellent organizational skills
  • Familiarity with analytical instrumentation such as, HSGC, FTIR, UV-Vis HPTLC a plus
  • Ability to troubleshot and perform maintenance of laboratory instrumentation under the supervision of laboratory management

Interpersonal

  • Good interpersonal skills, can work proficiently with people of different backgrounds, lifestyles, and values
  • Team attitude, willing to help others with their tasks and accept help with your tasks
  • Good communication skills, go out of the way to ensure proper understanding between communicating parties

Working Independently

  • Able to work independently when necessary
  • Able to self-manage one’s time for maximum efficiency
  • Able to complete a long-term project while simultaneously performing multiple smaller, shorter-term projects, or while performing routine QC testing