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Validation Chemist Jobs (NOW HIRING)

... validations) and stability studies. The Chemist III/Senior Chemist will execute chromatographic (LC/GC), spectroscopic and wet chemistry testing. As a senior member of the team, the Chemist III ...

Chemist Los Angeles, CA Full-Time, On-Site Overview We are seeking a detail-oriented and analytical ... Support method development, validation, and continuous improvement initiatives * Collaborate with ...

This role will provide production support to our Chemistry Lab and lead method development and validation of analytical instrumentation and processes. The Senior Chemist will also have responsibility ...

Analytical Chemistry Technician Location: Andover, MA Duration: 12 Months The Analytical Chemistry ... Write protocols and execute analytical method validations. Develop and execute testing protocols.

Chemist Los Angeles, CA Full-Time, On-Site Overview We are seeking a detail-oriented and analytical ... Support method development, validation, and continuous improvement initiatives * Collaborate with ...

... validation, or transfer experience • Manufacturing or plant support experience • Familiarity with LIMS and data trending or statistical analysis What We Offer • Competitive salary and benefits ...

Position Summary The Cement Chemist will play a key role in advancing RJ Lee Group's Concrete ... Develop and validate analytical methods for cement, SCMs, and concrete materials. * Provide expert ...

The chemist's primary initial role will be to validate analytical data, write data validation reports, and help prepare QAPPs. The right person with the right drive and attitude can grow into non ...

Position Summary The Cement Chemist will play a key role in advancing RJ Lee Group's Concrete ... Develop and validate analytical methods for cement, SCMs, and concrete materials. * Provide expert ...

Chemist This Chemist position supports a quality control laboratory by preparing, analyzing, and ... Strong data interpretation skills with the ability to review, validate, and summarize analytical ...

New

... validation, and execution of testing as needed • Write engineering test reports and final test reports Additional Information Regards Ria

Chemist

Hazelwood, MO · On-site +1

$91K - $141K/yr

District expert for chemistry matters related to feasibility studies and remedial investigations ... Must maintain a valid driver's license. Qualifications Who May Apply: US Citizens In order to ...

... validation of the new GPC test method Qualifications o Education - Minimum BS in Chemistry or ... related scientific degrees o Experience - Minimum 1 year in a regulated industry environment with a ...

Depending on experience, the Chemist may also lead method development and validation, support or oversee QA/QC programs, mentor other lab staff, and participate in audits and improvement projects.

Coatings Chemist

Chaska, MN · On-site

$61K - $90K/yr

... chemistry work related to the manufacture, scale-up, control, and continuous improvement of ... Ensures consistent execution of validated coating processes to meet safety, quality, and delivery ...

... chemistry work related to the manufacture, scale-up, control, and continuous improvement of ... Ensures consistent execution of validated coating processes to meet safety, quality, and delivery ...

Food Chemist

Atlanta, GA · On-site

$25 - $35/hr

Develop, validate, and optimize analytical methods , including sampling , monitoring , and ... Bachelor's degree in Chemistry or related field, or equivalent work experience. * 1-5 years of ...

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How much do validation chemist jobs pay per hour?

As of Jun 11, 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 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 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 are the key skills and qualifications needed to thrive in the Validation Chemist position, 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.

More about Validation Chemist jobs
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 June 2026, with employment types broken down into 33% Full Time, and 67% Contract. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $64,466 per year, or $31 per hour.
Chemist III/Sr. Chemist

Chemist III/Sr. Chemist

BioPhase Solutions

Anaheim, CA

$40 - $50/hr

Other

Posted 23 days ago


Job description

BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Chemist III/Senior Chemist to work for a leading Orange County area biotechnology company.
Pay Rate: $40-50/hour
Contract: 6+ months (with potential for conversion, but no guarantees)
Mon - Fri with flexible shift hours! Can be 1st or 2nd shift
Summary:
The Chemist III/Senior Chemist position will act as a senior member of the QC Analytical team, supporting raw material and finished product release, method qualifications (verifications, transfers, validations) and stability studies. The Chemist III/Senior Chemist will execute chromatographic (LC/GC), spectroscopic and wet chemistry testing. As a senior member of the team, the Chemist III/Senior Chemist will also assist with technical writing (Quality Investigations, Methods, Reports) and participate in lab improvement initiatives. Assists junior members of the team as chromatography trainer and technical expert.
Responsibilities:
  • Independently execute QC chemistry testing to support routine manufacturing activities, new product method development and stability testing.
  • Review analytical raw data
  • Participate in protocol design for qualification of new methods and subsequent authoring of new procedures.
  • Use technical expertise in LC/GC to troubleshoot new methods and improve existing procedures. Able to diagnose and make minor repairs.
  • Perform testing in compliance with relevant regulations. All activities are performed in GMP/GDP environment.
  • Assist in the performance of internal and external audits.
  • Assume role of SME and trainer for individual techniques/instrumentation, including chromatography.
  • Maintain the laboratory working areas in a clean and organized state.
  • Provide technical support to other departments within the organization.
  • Any and all other duties assigned by immediate supervisor.
Experience/Requirements:
  • Bachelors or Masters in Chemistry or related field
  • 5-8+ years of experience in a Chemistry and GMP QC Laboratory
  • Knowledge of quality systems, FDA and compendium requirements
  • Experience executing method qualifications in a GMP environment.
  • Experience with various analytical instruments/techniques (chromatography, spectroscopy, wet chemistry, etc.).
  • Demonstrated excellence in LC/GC analyses.
  • Experience with complex software programs preferred, but not required (Labware LIMS, Empower 3).
Please send resumes to tiffany@biophaseinc.com and visit our website at www.biophaseinc.com for additional job opportunities!!!