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Validation Chemist Jobs (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 ...

Chemist

Omaha, NE · On-site

Chemist The Chemist plays a key role in supporting pharmaceutical manufacturing by performing ... Carry out calibration, qualification, and validation of laboratory equipment and instruments as ...

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How much do validation chemist jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for validation chemist in the United States is $30.99, according to ZipRecruiter salary data. Most workers in this role earn between $24.04 and $35.58 per hour, depending on experience, location, and employer.

What does a validation chemist do?

A Validation Chemist ensures that laboratory instruments, analytical methods, and manufacturing processes comply with regulatory standards and produce consistent, reliable results. They develop and execute validation protocols, analyze data, and document findings to meet industry regulations such as FDA, GMP, and USP guidelines. Their work helps maintain product quality and safety in pharmaceutical, biotechnology, and chemical industries.

What does a typical day look like for a validation chemist, and how do they collaborate with other departments?

A typical day for a Validation Chemist involves planning and executing experiments to validate analytical methods, documenting results, and compiling comprehensive reports for regulatory compliance. They frequently collaborate with quality assurance, production, and research and development teams to ensure methods are robust and meet industry standards. Communication and teamwork are essential, as Validation Chemists often consult with other specialists to troubleshoot issues or optimize procedures. This collaborative environment ensures consistent product quality and helps drive continuous improvement within the organization.

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

To thrive as a Validation Chemist, you need a strong background in analytical chemistry, method validation, and laboratory best practices, typically supported by a degree in chemistry or a related field. Familiarity with laboratory instrumentation (such as HPLC, GC, and FTIR), regulatory guidelines (like FDA or ICH), and validation documentation systems is often required. Strong attention to detail, problem-solving skills, and effective collaboration with cross-functional teams are key soft skills in this position. These abilities ensure that all laboratory processes and products consistently meet quality standards and regulatory requirements.

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What cities are hiring for Validation Chemist jobs?

Cities with the most Validation Chemist job openings:

What states have the most Validation Chemist jobs?

States with the most job openings for Validation Chemist jobs include:

Infographic showing various Validation Chemist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 90% Full Time, 4% Part Time, and 5% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $64,466 per year, or $31 per hour.

Chemist - Method Development and Validation

Omnient Labs

Tempe, AZ • On-site

$60K - $70K/yr

Full-time

Posted 14 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