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Analytical Method Validation Jobs in Florida (NOW HIRING)

Analytical Chemist II

Tampa, FL · On-site

$65 - $90/hr

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 ...

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Sr. Chemist

Deerfield Beach, FL · On-site

$75K - $80K/yr

Support process validation, instrument validation, method validation, and analytical method development activities. * Prepare samples for testing by internal and external laboratories, as applicable.

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 ...

Conduct method validations, method transfers, and method suitability studies to ensure robustness, accuracy, and reproducibility of analytical procedures. * Investigate out-of-specification (OOS) and ...

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Analytical Method Validation information

See Florida salary details

$16

$38

$58

How much do analytical method validation jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for analytical method validation in Florida is $38.86, according to ZipRecruiter salary data. Most workers in this role earn between $29.47 and $47.26 per hour, depending on experience, location, and employer.

What is an analytical method validation?

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.

What does a typical day look like for someone working in analytical method validation?

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.

What are the key skills and qualifications needed to thrive in analytical method validation, and why are they important?

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.

What are popular job titles related to Analytical Method Validation jobs in Florida?

For Analytical Method Validation jobs in Florida, the most frequently searched job titles are:

Infographic showing various Analytical Method Validation job openings in Florida as of August 2026, with employment types broken down into 94% Full Time, 4% Part Time, and 2% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $80,821 per year, or $38.9 per hour.

Full-time

Posted 20 days ago


Job description

Job Summary: Laboratory position which involves development and validation of analytical methodology in support of the research projects involving testing of pharmaceutical components and/or drug products. Under general supervision, the position may require proficiency in support formulation, development method improvement and validation, testing per compendial pharmacopeia, etc.Job Responsibilities
  • Proficiency in multiple instrumentation techniques such as HPLC, GC, UV-VIS, dissolution equipment, pH measurement, titration, etc.
  • General knowledge of cGMP and FDA requirements.
  • Perform stability testing for GMP and R&D finished products
  • Conduct analytical testing of API, excipients and components  following compedial and validated methods
  • Perform analytical method validation and method transfer with a minimum supervision.
  • Follow company’s SOPs, STPS and comply with safety regulations.
  • Maintain detailed record of experiments in the laboratory notebook.
  • Timely communicate to supervisor(s) the obtained data and any issues aroused during testing
  • Ability to analyze and interpret the analytical data under minimum supervision.
  • Interpret specifications, standard operating procedures, and standard testing procedures.
  • Writes/reviews protocols, reports, SOPs and STPs applicable to analytical laboratory under the supervision.
  • Works as a member of a team to achieve all outcomes
  • Operates in accordance with our Code of Conduct and Business Ethics, and all established regulatory, compliance and safety requirements.
  • Performs all work in support of our Values: Collaboration, Courage, Perseverance, and Passion
  • All other relevant duties as assigned

Job Requirements

  • Education
    • Bachelor’s degree (B.S.) in chemistry or related field
    • Master’s degree (M.S.)
  • Knowledge, Skills and Abilities
  • General statistical applications such as normal ant T-test distribution, regression analysis, determination of test reliability and validity, analysis of variance, correlation techniques
  • Analytical chemistry and common instrumentation
  • General understanding of HPLC, GC, Drug Release, UV, IR, Titration.
  • Using common computer software and analytical applications programs.
  • Writing and interaction in English
  • Experience
    • At least two (2) to five (5) years experience in pharmaceutical laboratory (B.S)
    • At least zero (0) to three (3) years experience (M.S.)