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Validation Chemist Jobs (NOW HIRING)

WSP

Senior Chemist/Data Validator

Redmond, WA · On-site

Apply knowledge of analytical chemistry, environmental sampling design, laboratory methods, data validation principles, data quality objectives, UFP-QAPP requirements, laboratory QA/QC requirements ...

WSP

Senior Chemist/Data Validator

Redmond, WA · On-site

Apply knowledge of analytical chemistry, environmental sampling design, laboratory methods, data validation principles, data quality objectives, UFP-QAPP requirements, laboratory QA/QC requirements ...

WSP

Senior Chemist/Data Validator

Redmond, WA · On-site

Apply knowledge of analytical chemistry, environmental sampling design, laboratory methods, data validation principles, data quality objectives, UFP-QAPP requirements, laboratory QA/QC requirements ...

Adiabatic Materials

Senior Organic Chemist

Somerville, MA · On-site

$110K - $170K/yr

You'll develop new reactions, establish new routes to key targets, and validate where our chemistry can outperform conventional approaches. * Real ownership. As one of our early employees you'll have ...

Halff Associates, Inc.

Chemist

San Antonio, TX · On-site

Chemist, San Antonio, TX Halff is seeking a highly skilled and detail-oriented Chemist or Senior ... Review Level II and Level IV data validation packages on diverse environmental matrices (soil ...

Glatt Group

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 ...

Techtrueup

Chemist

Alpharetta, GA · On-site

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

Techtrueup

Chemist

Alpharetta, GA · On-site

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

Techtrueup

Chemist

Alpharetta, GA · On-site

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

Sotera Health Company

Chemist

Salt Lake City, UT · On-site

Develop, write, review, and validate SOPs, standard test procedures, protocols, and analytical ... D. in Chemistry preferred; or Bachelor's or master's degree in Chemistry or a closely related ...

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How much do validation chemist jobs pay per hour?

As of Sep 13, 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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Validation Chemist jobs near you
Infographic showing various Validation Chemist job openings in the United States as of September 2026, with employment types broken down into 91% Full Time, 4% Part Time, 1% Temporary, and 4% Contract. Highlights an 83% Physical, 4% Hybrid, and 13% Remote job distribution, with an average salary of $64,466 per year, or $31 per hour.

Chemist - Method Development / Method Validation

Oklahoma City, OK • On-site

ARL Bio Pharma
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about ARL Bio Pharmaexternal

$76K - $135K/yr

Full-time

Medical, Dental, Retirement

Re-posted 28 days ago

Key responsibilities

  • Develop and validate analytical methods for pharmaceutical samples.

  • Qualitatively and quantitatively test client samples using HPLC, IC, and LCMSMS.

  • Manage research projects and coordinate project-related work between departments.

Job description

Research amp; Development - Method Development / Method Validation Chemist
Position Summary...
Join a company where you can make a difference from day one and help make the world a better and safer place. ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry and is the most respected name in our industry. Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug manufacturers, and raw material suppliers bringing excellence to pharmaceutical sciences and making pharmaceuticals safer.
The position requires the performance of variety of task including development and validation of analytical method, work with HPLC (High Performance Liquid Chromatography), manage a variety of research projects, and qualitatively/quantitatively testing client samples. This position requires knowledge of commonly used concepts, practices, procedures, and instrumentation used in a chemistry laboratory. Research Scientist II manages projects with some supervision and reports to the lab supervisor. The Research Scientist II must be able to think and work independently, yet share ideas and work toward team goals. The ability to express thoughts in a clear concise manner both orally and written is also expected. Works to establish the ability to effectively prioritize and plan multiple work activities with varying deadlines and complexities.
Some highlights..
  • Attractive Relocation Package available!
  • Great Benefits
  • Excellent Work/Life Balance
  • Fantastic work environment
  • 100% Company-paid Medical and Dental Insurance
  • 401K Retirement with Company Match
This is a full-time role
Work Schedule: Days and hours of work are Monday through Friday, 8:30 a.m. to 5 p.m. Flexible hours such as early, late and weekend shift may be required.
Work Restrictions: Because of vital nature of this work, we do not allow medical marijuana cards and we do random drug testing on all of our employees.
Essential Functions...
  • Qualitatively and quantitatively test of client samples.
  • Development and validation of analytical methods.
  • Manage research projects and coordinate project related works between different departments of ARL.
  • Write research protocol, project report and working instruction.
  • Communication with client regarding the project/sample test status.
  • Use HPLC, IC and LCMSMS.
Position Requirements...
  • A BS in chemistry or related science with 4+ years industrial experience in MDMV Chemistry in the bio-technology and/or Pharmaceutical space.
  • PhD in chemistry with 4+ years industrial experience in MDMV Chemistry in the bio-technology and/or Pharmaceutical space preferred.
  • or related science with 0-2 years industrial experience
  • Communication Proficiency.
Work Environment...
This job operates in a laboratory environment.
Physical Demands...
This position often requires standing for prolong periods of time; dexterity in fingers and hands to perform complex and precise manipulations; ability to walk and stood; ability to lift and move up to 50 lbs; see in the normal visual range including the ability to distinguish colors and shades and hear in the normal audio range with or without correction.
AAP/EEO Statement
ARL Bio Pharma, Inc. provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, gender identity, national origin, disability, veteran status, genetics or any other characteristic protected by state, federal, or local law. ARL Bio Pharma, Inc. expressly prohibits any form of workplace harassment based on race, color, creed, religion, gender, age, sexual orientation, gender identity, national origin, disability, veteran status, genetics or any other characteristic protected by state, federal, or local law. Improper interference with the ability of ARL Bio Pharma, Inc. employees to perform their job duties may result in discipline up to and including discharge. Further, the company takes affirmative action to ensure that applicants and employees are treated without regard to any of these characteristics.

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