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Analytical Method Validation Jobs in Florida (NOW HIRING)

Eagle Labs, Inc

QC Microbiologist

Seminole, FL · On-site

$85K - $87K/yr

... analysts. They ensure all testing--such as sterility, bioburden, endotoxin, and environmental monitoring--complies with strict adherence to the GMP regulations. This role spans method validation ...

PL Developments

Analytical Scientist I

Doral, FL · On-site

The Analytical Scientist I will execute method transfer, verification, and validation activities, evaluate and interpret analytical data, and document results in compliance with cGMP and data ...

Synchrony Financial

AVP, Model Validation

Lake Mary, FL

$100K - $170K/yr

Serve as a key contributor and lead analyst performing model validation with minimal supervision ... Experience with Machine Learning / AI methodologies and related applications, including generative ...

Actalent

Microbiologist

Boca Raton, FL

Perform microbiological method validations and verifications, ensuring methods are robust, reliable ... Experience with data trending and analysis to support sterility assurance and contamination control ...

USAA

Director, Decision Science Analytics

Tampa, FL · On-site

Oversees and coordinates analytical tasks which include the evaluation of the business problem, analytical methodology, validation, documentation and presentation of findings and recommendations.

AVEVA DRUG DELIVERY SYSTEMS INC

QC Analyst I

Miramar, FL

$22 - $29.50/hr

Participates in testing to support Analytical Development method validations. Job Responsibilities • Supports release and stability testing for raw materials, components, standards, intermediate ...

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Analytical Method Validation information

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$16

$38

$58

How much do analytical method validation jobs pay per hour?

As of Aug 9, 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 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 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 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:
What job categories do people searching Analytical Method Validation jobs in Florida look for? The top searched job categories for Analytical Method Validation jobs in Florida are:
Analytical Method Validation jobs near you
Infographic showing various Analytical Method Validation job openings in Florida as of August 2026, with employment types broken down into 74% Full Time, 13% Part Time, and 13% Contract. Highlights an 100% In-person job distribution, with an average salary of $80,821 per year, or $38.9 per hour.

QC Microbiologist

Eagle Labs, Inc

Seminole, FL • On-site

$85K - $87K/yr

Full-time

Posted 15 days ago

Job description

Quality Control Microbiology Supervisor

Overview:

Quality Control (QC) Microbiology Supervisor oversees daily microbiology laboratory operations and a team of analysts. They ensure all testing—such as sterility, bioburden, endotoxin, and environmental monitoring—complies with strict adherence to the GMP regulations. This role spans method validation, root-cause investigations, and data integrity verification.

Key Duties:

These are only highlighted by major key duties. Other requested duties assigned by Eagle Labs, Inc for job function by Quality Control Manager, Director of Laboratory Operations, or Executive leadership.

  • Scheduling, conducting OOS (Out-of-Specification) investigations, and managing staff training scheduling, conducting investigations, and managing staff training.
  • Supervises routine testing, including sterility testing, bacterial endotoxins (BET), bioburden, microbial limits, and growth promotion of media.
  • Support assay method verification, transfer, and equipment qualification within the Laboratory.
  • Act as a subject matter expert (SME) during internal audits and regulatory inspections.
  • Lead Out-of-Specification (OOS) investigations, initiate Corrective and Preventive Actions (CAPA), and implement change controls.

Core Responsibilities:

  • Team Leadership & Development: Supervise, train, and mentor laboratory analysts. Manage scheduling, performance evaluations, and gowning/aseptic qualifications.
  • Testing Oversight: Oversee and review routine microbiological assays, including sterility, bioburden, bacterial endotoxins (LAL), microbial identification (e.g., MALDI-TOF), and water testing.
  • Environmental Monitoring (EM): Approve EM data, analyze trending reports, and monitor classified cleanroom utilities to maintain compliance.

Qualifications & Requirements

  • Education: Bachelor’s degree in microbiology, Biology, or a closely related life science discipline.
  • Experience: Minimum 5 years of hands-on experience in a cGMP pharmaceutical or biotech microbiology laboratory, including at least 3 or more years in a lead or supervisory capacity.
  • Technical Skills: Advanced understanding of aseptic processing, cleanroom behaviors, and compendial requirements (USP, EP, JP).
  • Soft Skills: Strong problem-solving, data trending capabilities, and excellent verbal and written communication skills.