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Validation Chemist Jobs (NOW HIRING)

Actalent

Chemist

La Verne, CA

$37 - $42/hr

The position also supports method validation and transfer, maintains laboratory documentation under ... Perform chemistry testing of raw materials, in-process samples, final products, validation-related ...

Actalent

Chemist

La Verne, CA

The position also supports method validation and transfer, maintains laboratory documentation under ... Perform chemistry testing of raw materials, in-process samples, final products, validation-related ...

Actalent

Chemist

La Verne, CA

The position also supports method validation and transfer, maintains laboratory documentation under ... Perform chemistry testing of raw materials, in-process samples, final products, validation-related ...

synergy

Chemist

Dallas, TX · On-site

Chemist Synergy is looking for a motivated Chemist to join our dynamic team. The ideal candidate ... Develop, optimize, and validate analytical methods. * Maintain accurate and detailed records of ...

synergy

Chemist

Dallas, TX · On-site

Chemist Synergy is looking for a motivated Chemist to join our dynamic team. The ideal candidate ... Develop, optimize, and validate analytical methods. * Maintain accurate and detailed records of ...

Bhate Environmental Associates, Inc.

Chemist

Denver, CO · On-site

Validate analytical chemical data in accordance with DoD, USEPA National, USEPA Regional, and State guidelines. * Prepare Quality Assurance Project Plans (QAPPs), Data Validation Reports (DVRs) and ...

synergy

Chemist

Dallas, TX · On-site

Chemist Synergy is looking for a motivated Chemist to join our dynamic team. The ideal candidate ... Develop, optimize, and validate analytical methods. * Maintain accurate and detailed records of ...

Catalyst Nutraceuticals

Chemist

Buford, GA · On-site

The chemist will also be an integral part of laboratory expansion efforts by aiding in method development and validation projects. The position will report to the Laboratory Manager. The position is ...

Apothecus Pharmaceutical Corp.

Chemist

Hicksville, NY · On-site

We're seeking a Quality Control Chemist to join our team. This is an exciting opportunity for an ... stability batches following validated methods and established specifications. * Apply USP ...

SuperbTech,Inc.

Chemist

Culver City, CA

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 ...

Onsite Personnel LLC

Chemist

Philadelphia, PA

Summary: QC Chemist: This position's purpose is to support the Quality Control lab for analysis of ... Experience in quality systems, including validation, documentation, compliance department preferred.

Farmina Pet Foods

Chemist

Reidsville, NC · On-site

Our mission is to develop the best all-natural, nutritious, and scientifically validated food that ... Position Purpose The Chemist will conduct analytical testing and laboratory operations to ensure ...

Furniture of Dalton

Chemist

Chatsworth, GA · On-site

... 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 package ...

SuperbTech

Chemist

Culver City, CA

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 ...

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All JobsValidation Chemist Jobs

Validation Chemist information

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How much do validation chemist jobs pay per hour?

As of Jun 10, 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.

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Validation Chemist jobs near you
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 - Method Development / Method Validation

Chemist - Method Development / Method Validation

ARL Bio Pharma

Oklahoma City, OK • On-site

$76K - $135K/yr

Full-time

Medical, Dental, Retirement

Posted 22 days ago

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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