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Method Validation Chemist Jobs (NOW HIRING)

Chemist

Ramsey, NJ · On-site

$70K - $90K/yr

Write analytical method validation, verification, transfer and stability protocols and reports. Provide training and mentoring to chemists. May supervise chemists on project basis. Must maintain a ...

Quality Control Chemist II Location: Johns Creek, GA - Onsite Duration: 12 months, with potential ... The successful candidate will be responsible for analytical method development, validation and ...

Quality Control Chemist II Location: Johns Creek, GA - Onsite Duration: 12 months, with potential ... The successful candidate will be responsible for analytical method development, validation and ...

Quality Control Chemist II Location: Johns Creek, GA - Onsite Duration: 12 months, with potential ... The successful candidate will be responsible for analytical method development, validation and ...

We are seeking a Chemistry Laboratory Analyst to perform advanced analytical testing on raw ... Develop, validate, and improve laboratory test methods , sampling procedures, monitoring systems ...

The scope of work includes process and test method validation, identifying and implementing process ... Oversee junior chemists' execution of equipment and processes validations. * Review, modify, and ...

Execute analytical method validations, method transfers, and periodic method reviews in accordance with applicable procedures and regulatory requirements. * Support method transfers between internal ...

Execute analytical method validations, method transfers, and periodic method reviews in accordance with applicable procedures and regulatory requirements. * Support method transfers between internal ...

Execute analytical method validations, method transfers, and periodic method reviews in accordance with applicable procedures and regulatory requirements. * Support method transfers between internal ...

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Method Validation Chemist information

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$49

How much do method validation chemist jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for method validation chemist in the United States is $31.50, according to ZipRecruiter salary data. Most workers in this role earn between $24.76 and $36.06 per hour, depending on experience, location, and employer.

What is a method validation chemist?

Method Validation Chemists are professionals who develop, validate, and document analytical methods to ensure they produce reliable and consistent results. They work primarily in pharmaceutical, food, environmental, and chemical industries to confirm that laboratory testing methods meet regulatory requirements and quality standards. Their responsibilities include designing validation protocols, performing experiments, analyzing data, and reporting results to ensure accuracy and compliance. Method Validation Chemists play a critical role in product safety and quality assurance.

What skills and qualifications are needed to be a method validation chemist?

To thrive as a Method Validation Chemist, you need a strong background in analytical chemistry, experience with laboratory techniques, and a relevant degree in chemistry or a related field. Familiarity with instrumentation such as HPLC, GC, and spectrophotometers, as well as knowledge of regulatory guidelines like ICH and FDA, is typically required. Attention to detail, strong problem-solving abilities, and effective communication skills help distinguish top performers in this role. These skills and qualities are essential for ensuring accurate, reliable results and maintaining regulatory compliance in pharmaceutical and scientific laboratories.

What are common challenges faced by method validation chemists during the validation process?

Method Validation Chemists often encounter challenges such as ensuring the accuracy and precision of analytical methods across a wide range of sample matrices. Troubleshooting unexpected results, dealing with instrument variability, and meeting strict regulatory requirements (like those from the FDA or EMA) are also frequent hurdles. Additionally, coordinating with cross-functional teams—such as quality assurance, production, and regulatory affairs—requires strong communication and organizational skills. Successfully navigating these challenges is integral to delivering reliable and compliant validation reports.

What cities are hiring for Method Validation Chemist jobs?

Cities with the most Method Validation Chemist job openings:

What states have the most Method Validation Chemist jobs?

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

What are popular job titles related to Method Validation Chemist jobs?

For Method Validation Chemist jobs, the most frequently searched job titles are:

Chemist

Ramsey, NJ • On-site

$70K - $90K/yr

Other

Posted 13 days ago


Key responsibilities

  • Support multiple projects by conducting analytical testing and developing/validating analytical methods.

  • Write, review, and revise protocols, reports, and SOPs related to analytical methods and validation processes.

  • Supervise, train, and mentor chemists and laboratory personnel, and maintain laboratory records in compliance with regulations.


Job description

We are a leading world supplier of integrated processing solutions for customers in the area of pharmaceuticals, food processing, feeds and fine chemicals. Our products and services stand for reliability and quality worldwide. About 3,000 employees work for Glatt at more than 15 companies and offices all over the world.

Chemist / Senior Chemist

Responsible for supporting multiple projects under limited supervision. Provide scientific expertise and ability to independently investigate and resolve analytical problems/issues. Write analytical method validation, verification, transfer and stability protocols and reports. Provide training and mentoring to chemists. May supervise chemists on project basis. Must maintain a high degree of flexibility to accommodate fluctuating priorities in a fast‑paced environment.

Responsibilities:
  • Supervise a small staff of chemists on project basis.
  • Train laboratory personnel in the use of equipment and analytical techniques.
  • Write, review and revise SOP’s, method validation, verification, transfer and stability protocols and reports as required.
  • Develop/transfer and validate/verify analytical methods as necessary.
  • Conduct analytical testing in compliance with applicable methods, protocols, SOP’s and regulatory agency guidelines.
  • Maintain laboratory records per CGMPs regulations and in compliance with applicable SOP’s.
  • Peer review data and reports in accordance with applicable Test Monographs, Protocols and SOP’s.
  • Recognize deviations from normal results and inform VP, Quality Control & Development of any out of specification (OOS) results and/or deviations that may affect the integrity of the data and drive corrective action of problems.
  • Review and revise laboratory systems on an ongoing basis.
  • Other responsibilities as assigned by the VP, Quality Control & Development.
Qualifications:
  • Bachelor’s degree in Chemistry, Physical Chemistry, Chemical Engineering, Biology, or related sciences with 7–10 years of experience in a GMP‑compliant pharmaceutical environment.
  • Master’s or Ph.D. in a relevant scientific field with 5–7 years of experience in a GMP environment.
  • Advanced chromatography skills.
  • Strong hands‑on experience with HPLC (High‑Performance Liquid Chromatography) and GC (Gas Chromatography) equipment, including maintenance and troubleshooting.
  • Strong knowledge and experience in dissolution techniques.
  • Proficient with Microsoft Office and data acquisition software.
  • In‑depth understanding of analytical methods, product specifications, and historical data. Ability to independently investigate and resolve analytical issues.
  • Skilled in writing validation, verification, transfer, and stability protocols and reports.
  • Strong analytical and problem‑solving abilities.
  • High attention to detail and accuracy.
  • Ability to prioritize, multitask, and meet deadlines with minimal supervision.
  • Excellent communication, interpersonal, and presentation skills.

Salary Range:

$70,000-$90,000

You have the opportunity to perform an interesting and responsible job in a successful, renowned company. If this interesting position appeals to you, we look forward to receiving your online application. Applications that do not reach us personally via the online portal can unfortunately not be considered.

Glatt Air Techniques Inc., Human Resources, 20 Spear Road, Ramsey, NJ 07446, USA www.glatt.com

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