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Fda Chemist information
See salary details
$17.31 - $20.54
7% of jobs
$20.54 - $23.78
16% of jobs
$24.02 is the 25th percentile. Wages below this are outliers.
$23.78 - $27.01
21% of jobs
The median wage is $28.02 / hr.
$27.01 - $30.24
17% of jobs
$30.24 - $33.48
13% of jobs
$33.68 is the 75th percentile. Wages above this are outliers.
$33.48 - $36.71
9% of jobs
$36.71 - $39.95
7% of jobs
$39.95 - $43.18
4% of jobs
$43.18 - $46.42
2% of jobs
$46.42 - $49.65
2% of jobs
$49.65 - $52.88
1% of jobs
$17
$30
$52
How much do fda chemist jobs pay per hour?
As of Sep 6, 2026, the average hourly pay for fda 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 is an FDA chemist?
An FDA Chemist is a scientist who ensures the safety, quality, and efficacy of food, drugs, and other regulated products. They conduct laboratory tests, analyze chemical compositions, and ensure compliance with federal regulations. Their work helps prevent contamination, ensure accurate labeling, and support public health initiatives. FDA Chemists may specialize in areas such as pharmaceuticals, food safety, or forensic chemistry.
What are the key skills and qualifications needed to thrive as an FDA chemist?
To thrive as an FDA Chemist, you need a strong background in chemistry or a related science, typically supported by at least a bachelor's degree and experience with analytical laboratory techniques. Familiarity with laboratory instruments like HPLC, GC, and ICP-MS, as well as knowledge of regulatory guidelines such as GMP and GLP, is essential. Attention to detail, problem-solving skills, and effective written and verbal communication are important soft skills for excelling in this role. Mastering these abilities ensures accurate analysis, compliance with regulations, and collaboration within multidisciplinary teams handling critical food and drug safety issues.
What types of projects or products do FDA chemists typically work on, and how is their work collaborative?
FDA Chemists commonly work on testing pharmaceuticals, food products, medical devices, and cosmetics to ensure they comply with safety and quality standards. Their daily work involves conducting analytical tests, interpreting results, documenting findings, and contributing to investigations when issues arise. Collaboration is frequent, as chemists often work alongside microbiologists, quality control specialists, and regulatory affairs professionals to resolve complex problems and ensure regulatory compliance. This team-oriented environment fosters professional growth, as chemists can expand their expertise through interdisciplinary projects and increased responsibility over time.
Are pharmaceutical chemists in demand?
Pharmaceutical chemists are in steady demand due to the ongoing need for new drug development, quality control, and regulatory compliance in the healthcare industry. Employment opportunities are expected to grow as the pharmaceutical sector expands and advances in research and technology continue. Strong knowledge of chemistry, laboratory skills, and relevant certifications enhance job prospects in this field.
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Full-time
Re-posted 17 days ago
Key responsibilities
Perform laboratory testing of raw materials, in-process, release, and stability samples for drug products.
Develop, validate, and transfer analytical methods for testing pharmaceutical products and related substances.
Document testing results, perform peer reviews, and generate analytical reports.
Lannett rating
7.8
Based on 9 frontline employees who took The Breakroom Quiz
50th of 86 rated pharmaceutical
Job description
Description:
Summary
This position is primarily responsible for the laboratory testing of raw materials, packaging materials, in-process, release and stability samples for developmental and pre-commercial drug products, including the evaluation of new raw materials, new packaging materials, reference standard qualifications, method transfers, and develop and validate methods within the framework of cGMP compliance guidelines.
Responsibilities
· Perform routine and non-routine physical and chemical tests and assays on raw materials, API’s, in-process, finished products, experimental batches and associated stability studies
· Testing performed to include basic and complex lab equipment and procedures, such as pH, Loss on Drying, Residue on Ignition, Water Content by Karl Fischer, Assay/Impurities by HPLC, Dissolution, Residual Solvents by GC, and wet chemistry techniques such as titrations and sample derivatizations
· Conduct analytical research and develop analytical methods to test pharmaceutical products for conformance to established specifications with some supervision.
· Develop and validate analytical test methods for assay, dissolution, preservatives in drug products according to ICH/FDA/USP requirements with minimal to no supervision.
· Develop and validate test methods for residual solvents and impurities/degradation products in drug substances/excipients/drug products according to ICH/FDA/USP requirements under some supervision
· Develop and validate analytical Cleaning Validation methods and perform testing of cleaning validation samples and generate analytical report with minimum supervision.
· Multi-task by working on several simultaneous projects. Develop project timelines.
· Document all laboratory testing and maintain accurate and legible notebooks and records
· Perform peer review on other analysts’ data.
· Provide regular update progress reports of projects
· Comply with all relevant regulatory requirements
· At all times strive to maintain the self-esteem of individual team members and the professionalism of the group as a whole
· Perform laboratory troubleshooting, propose solutions and implement
· Other projects and duties as required or assigned
· Provide technical input for purchase of new/updated laboratory instruments and software systems
· Train other laboratory chemists on analytical instrumentation and methods.
Mentor/Train team members on new/revised skills and testing procedures
Requirements:Experience
- BS Degree in Chemistry or related field and 4 – 8 years of pharmaceutical product analysis experience in a cGMP-regulated lab environment
Skills
- Experience working in the pharmaceutical industry and/or analytical laboratory
- Knowledge of cGMP, USP/NF, and FDA guidelines and regulations
- Expertise in analytical methods and lab instrumentation (e.g. HPLC, GC, dissolution, wet chemistry)
- Demonstrated ability to perform method development and validation in accordance with ICH regulations with minimal supervision
- Excellent oral and written communication skills
- Strong organization, time management, leadership and troubleshooting skills
- Demonstrated ability to work as part of a cross-functional team
- Basic knowledge in Microsoft Word and Excel
- Experience with software associated with a Laboratory Information Management System (LIMS) and a Chromatography Data System (CDS)
About LANNETT
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Philadelphia, PA, US
Year founded
1942