Performs method validation, method transfer, verification, and analytical troubleshooting. * Investigates Out of Specification (OOS), Out of Trend (OOT), deviations, and laboratory non-conformances.
Quick apply
Performs method validation, method transfer, verification, and analytical troubleshooting. * Investigates Out of Specification (OOS), Out of Trend (OOT), deviations, and laboratory non-conformances.
Quick apply
Performs method validation, method transfer, verification, and analytical troubleshooting. * Investigates Out of Specification (OOS), Out of Trend (OOT), deviations, and laboratory non-conformances.
The position supports process improvements, method validation, and training initiatives. What You Will Do * Perform routine and moderately complex chemical analyses, including HPLC, assay, potency ...
The position supports process improvements, method validation, and training initiatives. What You Will Do * Perform routine and moderately complex chemical analyses, including HPLC, assay, potency ...
Tampa, FL · On-site
The position supports process improvements, method validation, and training initiatives. What You Will Do * Perform routine and moderately complex chemical analyses, including HPLC, assay, potency ...
Tampa, FL · On-site
The position supports process improvements, method validation, and training initiatives. What You Will Do * Perform routine and moderately complex chemical analyses, including HPLC, assay, potency ...
Conduct analytical testing, method qualifications, and method validations to support GMP manufacturing and the implementation of new testing and assessment procedures * Coordinate validation and pre ...
Conduct analytical testing, method qualifications, and method validations to support GMP manufacturing and the implementation of new testing and assessment procedures * Coordinate validation and pre ...
Conduct analytical testing, method qualifications, and method validations to support GMP manufacturing and the implementation of new testing and assessment procedures * Coordinate validation and pre ...
Conduct analytical testing, method qualifications, and method validations to support GMP manufacturing and the implementation of new testing and assessment procedures * Coordinate validation and pre ...
Conduct analytical testing, method qualifications, and method validations to support GMP manufacturing and the implementation of new testing and assessment procedures * Coordinate validation and pre ...
Conduct analytical testing, method qualifications, and method validations to support GMP manufacturing and the implementation of new testing and assessment procedures * Coordinate validation and pre ...
Tampa, FL · On-site
Support method and equipment validation through data compilation, statistical analysis, and reporting. * Prepare data packages for internal, client, and regulatory audits; respond to data-related ...
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Tampa, FL · On-site
Support method and equipment validation through data compilation, statistical analysis, and reporting. * Prepare data packages for internal, client, and regulatory audits; respond to data-related ...
Saint Petersburg, FL · On-site
$93K - $118K/yr
Independently develop, validate, and routinely execute instrumental test methods in support of Drug Substances and Drug Products; analyze data, document results in accordance with cGMP and internal ...
Saint Petersburg, FL · On-site
$93K - $118K/yr
Independently develop, validate, and routinely execute instrumental test methods in support of Drug Substances and Drug Products; analyze data, document results in accordance with cGMP and internal ...
Performs practical laboratory work including method development, method validation, and ... analysis and CAPA development. * Provides data reports, summaries, and metrics to support ...
Quick apply
Performs practical laboratory work including method development, method validation, and ... analysis and CAPA development. * Provides data reports, summaries, and metrics to support ...
Saint Petersburg, FL · On-site
$93K - $118K/yr
Independently develop, validate, and routinely execute instrumental test methods in support of Drug Substances and Drug Products; analyze data, document results in accordance with cGMP and internal ...
Saint Petersburg, FL · On-site
$93K - $118K/yr
Independently develop, validate, and routinely execute instrumental test methods in support of Drug Substances and Drug Products; analyze data, document results in accordance with cGMP and internal ...
Participate in internal audits, proficiency testing (PT), and method validation studies. Collaborate with QA officers, senior analysts, and cross-functional teams on non-routine investigations ...
Participate in internal audits, proficiency testing (PT), and method validation studies. Collaborate with QA officers, senior analysts, and cross-functional teams on non-routine investigations ...
Participate in internal audits, proficiency testing (PT), and method validation studies. Collaborate with QA officers, senior analysts, and cross-functional teams on non-routine investigations ...
Participate in internal audits, proficiency testing (PT), and method validation studies. Collaborate with QA officers, senior analysts, and cross-functional teams on non-routine investigations ...
Participate in internal audits, proficiency testing (PT), and method validation studies. Collaborate with QA officers, senior analysts, and cross-functional teams on non-routine investigations ...
Participate in internal audits, proficiency testing (PT), and method validation studies. Collaborate with QA officers, senior analysts, and cross-functional teams on non-routine investigations ...
Orlando, FL · On-site
Participate in internal audits, proficiency testing (PT), and method validation studies. * Collaborate with QA officers, senior analysts, and cross-functional teams on non-routine investigations ...
Orlando, FL · On-site
Participate in internal audits, proficiency testing (PT), and method validation studies. * Collaborate with QA officers, senior analysts, and cross-functional teams on non-routine investigations ...
Orlando, FL · On-site
Participate in internal audits, proficiency testing (PT), and method validation studies. * Collaborate with QA officers, senior analysts, and cross-functional teams on non-routine investigations ...
Orlando, FL · On-site
Participate in internal audits, proficiency testing (PT), and method validation studies. * Collaborate with QA officers, senior analysts, and cross-functional teams on non-routine investigations ...
Orlando, FL · On-site
Participate in internal audits, proficiency testing (PT), and method validation studies. * Collaborate with QA officers, senior analysts, and cross-functional teams on non-routine investigations ...
Orlando, FL · On-site
Participate in internal audits, proficiency testing (PT), and method validation studies. * Collaborate with QA officers, senior analysts, and cross-functional teams on non-routine investigations ...
Participate in internal audits, proficiency testing (PT), and method validation studies. Collaborate with QA officers, senior analysts, and cross-functional teams on non-routine investigations ...
Participate in internal audits, proficiency testing (PT), and method validation studies. Collaborate with QA officers, senior analysts, and cross-functional teams on non-routine investigations ...
Development, optimization, validation/qualification, and tech transfer of analytical test methods and bioanalytical assays such as ELISA, spectrophotometric, chromatographic, gel-based, enzymatic ...
Development, optimization, validation/qualification, and tech transfer of analytical test methods and bioanalytical assays such as ELISA, spectrophotometric, chromatographic, gel-based, enzymatic ...
Participate in internal audits, proficiency testing (PT), and method validation studies. Collaborate with QA officers, senior analysts, and cross-functional teams on non-routine investigations ...
Participate in internal audits, proficiency testing (PT), and method validation studies. Collaborate with QA officers, senior analysts, and cross-functional teams on non-routine investigations ...
Orlando, FL · On-site
Participate in internal audits, proficiency testing (PT), and method validation studies. * Collaborate with QA officers, senior analysts, and cross-functional teams on non-routine investigations ...
Orlando, FL · On-site
Participate in internal audits, proficiency testing (PT), and method validation studies. * Collaborate with QA officers, senior analysts, and cross-functional teams on non-routine investigations ...
$16.89 - $20.66
2% of jobs
$20.66 - $24.43
6% of jobs
$24.43 - $28.20
13% of jobs
$29.38 is the 25th percentile. Wages below this are outliers.
$28.20 - $31.98
13% of jobs
$31.98 - $35.75
11% of jobs
The median wage is $37.63 / hr.
$35.75 - $39.52
12% of jobs
$39.52 - $43.29
9% of jobs
$46.20 is the 75th percentile. Wages above this are outliers.
$43.29 - $47.07
13% of jobs
$47.07 - $50.84
13% of jobs
$50.84 - $54.61
6% of jobs
$54.61 - $58.38
3% of jobs
$16
$38
$58
To thrive in Analytical Method Validation, you need a strong background in analytical chemistry or related sciences, precision in laboratory work, and experience with method development and validation protocols, often supported by a relevant degree. Familiarity with instrumentation such as HPLC, GC, and mass spectrometry, as well as knowledge of regulatory standards like ICH, FDA, or USP, and proficiency in laboratory information management systems (LIMS) are key. Attention to detail, critical thinking, and effective communication are important soft skills for troubleshooting and collaborating with cross-functional teams. These skills ensure robust, compliant analytical methods that underpin product quality and regulatory approval.
An Analytical Method Validation job involves developing, assessing, and documenting laboratory methods to ensure they produce reliable and accurate results. Professionals in this role validate methods according to regulatory guidelines (such as ICH, USP, or FDA) by evaluating parameters like accuracy, precision, specificity, and robustness. They work in industries like pharmaceuticals, biotechnology, and chemicals to ensure compliance with quality standards. The role also requires troubleshooting analytical issues and maintaining validation records to support regulatory audits.
A typical day in Analytical Method Validation involves developing and executing protocols to verify that laboratory methods are reliable, accurate, and consistent with industry regulations. You'll spend time in the lab conducting experiments, analyzing sample data, documenting results, and preparing detailed validation reports for regulatory submission. Collaborating with quality assurance, regulatory teams, and other scientists is common to address findings and ensure alignment with project goals. This role combines hands-on technical work with critical data review and cross-disciplinary teamwork, offering a dynamic and intellectually engaging work environment.

Senior Chemist – Quality Control
Key Responsibilities:
Complies with all cGLP/GMP and safety requirements, laboratory SOPs, and Company policies.
Ensures compliance with good housekeeping and laboratory safety practices.
Performs advanced chemical analysis and testing of raw materials, in-process samples, finished products, and stability samples.
Operates, calibrates, troubleshoots, and maintains analytical instrumentation including HPLC, GC, ICP, UV-Vis, FTIR, titrators, and dissolution equipment.
Reviews and approves laboratory data, calculations, and analytical documentation to ensure accuracy and compliance.
Performs method validation, method transfer, verification, and analytical troubleshooting.
Investigates Out of Specification (OOS), Out of Trend (OOT), deviations, and laboratory non-conformances.
Prepares sample solutions, reagents, standards, and volumetric solutions according to SOPs and cGMP requirements.
Maintains appropriate documentation, laboratory notebooks, and records in compliance with cGLP and cGMP standards.
Supports internal and external audits, FDA inspections, and regulatory compliance activities.
Assists in the development and revision of SOPs, specifications, test methods, and laboratory procedures.
Trains and mentors QC Chemists, Laboratory Technicians, and junior staff.
Coordinates laboratory activities and assists management with scheduling and workload prioritization.
Maintains inventory control of laboratory supplies, chemicals, standards, and reagents.
Ensures proper disposal of hazardous waste according to EPA regulations.
Performs related duties as assigned by management.
Qualifications:
Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related scientific field required.
Minimum of 5+ years of experience in a pharmaceutical, nutraceutical, food, or regulated laboratory environment.
Strong knowledge of cGMP, cGLP, FDA regulations, and laboratory safety practices.
Experience with analytical instrumentation such as HPLC, GC, ICP, UV, FTIR, and titrators.
Experience performing analytical method validation and troubleshooting.
Strong documentation, investigation, and technical writing skills.
Bilingual (English and Spanish) preferred.
Strong mathematical, analytical, and problem-solving skills.
Ability to work independently and in a fast-paced environment.
Leadership and mentoring experience preferred.
Other Requirements:
Must be available Monday to Friday from 8:00 AM to 4:30 PM.
Ability to occasionally lift up to 50 pounds.
Physical Requirements:
Requires standing, bending, lifting, handling chemicals, and prolonged computer use.
Work Environment:
Works frequently in a laboratory and manufacturing environment.
Exposure to chemicals, laboratory equipment, and regulated production areas.
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