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Fda Scientist Jobs in Florida (NOW HIRING)

Danaher

Principal Clinical Scientist

Miami, FL · On-site +1

Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA 510(k)/PMA, CEIVDR) across multiple diagnostic modalities. * Act as a scientific and clinical ...

Jj

Sr. Sterilization Scientist

Palm Beach Gardens, FL

$86K - $118K/yr

Quality Job Sub Function: R&D/Scientific Quality Job Category: Professional All Job Posting ... Solid understanding of EU, FDA, cGMP and cGLP regulations. Other: * Up to 10% domestic travel may ...

Danaher

Development Scientist II

Miami, FL · On-site

Experience working in an FDA / ISO 13485 regulated environment. * Working knowledge of basic ... Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner ...

Danaher

Development Scientist II

Miami, FL · On-site

Experience working in an FDA / ISO 13485 regulated environment. * Working knowledge of basic ... Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner ...

Danaher

Development Scientist II

Miami, FL

Experience working in an FDA / ISO 13485 regulated environment. * Working knowledge of basic ... Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner ...

Danaher

Development Scientist II

Miami, FL

Experience working in an FDA / ISO 13485 regulated environment. * Working knowledge of basic ... Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner ...

CEDENT

Formulation Scientist

Largo, FL

This individual must have extensive cGMP experience and FDA and ICH Guidance experience. Must be able to provide leadership and mentoring to I&D Interns, Associates, and Formulator I(s). MAJOR DUTIES ...

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$83.2K

$102.8K

How much do fda scientist jobs pay per year?

As of Aug 23, 2026, the average yearly pay for fda scientist in Florida is $83,206.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,600.00 and $102,400.00 per year, depending on experience, location, and employer.

What is an FDA Scientist?

An FDA Scientist is a researcher or regulatory expert responsible for evaluating the safety, efficacy, and quality of pharmaceutical drugs, medical devices, biologics, and food products. They conduct laboratory research, review clinical trial data, and assess regulatory submissions to ensure compliance with federal laws and guidelines. FDA Scientists play a critical role in protecting public health by making science-based decisions on product approvals and safety standards.

What types of projects and responsibilities can I expect as an FDA Scientist?

As an FDA Scientist, you'll typically be involved in reviewing data from clinical trials, conducting laboratory research, evaluating the safety and efficacy of pharmaceuticals or medical devices, and preparing reports for regulatory submissions. You'll collaborate closely with multidisciplinary teams including chemists, statisticians, and regulatory specialists to ensure scientific rigor and adherence to federal standards. Some days may involve detailed data analysis, while others could require participating in cross-team meetings or interacting with external stakeholders. This dynamic environment offers opportunities to contribute to important public health decisions and develop specialized expertise over time.

What are the key skills and qualifications needed to thrive in the FDA Scientist position, and why are they important?

To thrive as an FDA Scientist, you need a solid background in biology, chemistry, pharmacology, or a related scientific field, typically supported by at least a bachelor's or advanced degree. Familiarity with regulatory submission systems, laboratory information management systems (LIMS), and relevant certifications such as Good Laboratory Practice (GLP) or Good Clinical Practice (GCP) is important. Strong analytical thinking, attention to detail, and effective communication skills help you excel when collaborating with colleagues and presenting findings. These abilities ensure accurate data review and regulatory compliance, which are crucial for advancing public health and safety.

How much do FDA scientists make?

FDA scientists typically earn between $70,000 and $130,000 annually, depending on experience, education, and location. Entry-level positions often start around $70,000, while experienced scientists with advanced degrees can earn higher salaries, especially in supervisory or specialized roles.

What are the most commonly searched types of Fda Scientist jobs in Florida?

The most popular types of Fda Scientist jobs in Florida are:

What are popular job titles related to Fda Scientist jobs in Florida?

For Fda Scientist jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Fda Scientist jobs in Florida look for?

The top searched job categories for Fda Scientist jobs in Florida are:

Fda Scientist jobs near you
Infographic showing various Fda Scientist job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 3% Contract, and 1% Nights. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $83,206 per year, or $40 per hour.

Scientist I, Analytical Development

ADMA BIOMANUFACTURING LLC

Boca Raton, FL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 28 days ago

Job description

Scientist I, Analytical Development
Job Description:
Position Summary:
The Scientist I, Analytical Development demonstrates success in technical proficiency, scientific creativity, collaboration with others and independent thought. As a key member of the Analytical Development group provide analytical support for process development group and manufacturing. Be responsible for the development, implementation and execution of routine analytical techniques for protein quantification and characterization.
Essential Functions and Responsibilities:
  • Development, optimization, validation/qualification, and tech transfer of analytical test methods and bioanalytical assays such as ELISA, spectrophotometric, chromatographic, gel-based, enzymatic activity and chromogenic assays.
  • Design, development, and hands-on execution of analytical studies to support protein characterization and quantitation.
  • Perform experiments as needed to generate data for validations and other special projects.
  • Evaluate and interpret test and experimental data generated from development/qualification and validation work using Excel or other software as required.
  • Collaborate cross-functionality with other departments to select, qualify, and implement reference standards.
  • Execute assigned tasks within the constraints of timelines, under minimal supervision by senior scientific staff.
  • Troubleshoots technical procedures, methodology and instrumentation.
  • Perform instrument calibration or qualification according to written procedures.
  • Serve as primary authors, reviewers, and approvers of regulated documents such as method validation/qualification reports, protocols, transfers, SOPs, change controls, investigational reports, and deviations.
  • Experience in writing technical reports and presenting findings to internal or external clients.
  • Review and/or approve cGMP documentation generated by other analysts in the laboratory if necessary.
  • Accountable for following Standard Operating Procedures (SOPs), adhering to cGMP guidelines and all relevant compliance regulations.
  • Use judgment, creativity, and sound technical knowledge to obtain and recommend solutions to problems as directed by AD management.
  • Maintain current knowledge in field of expertise and develop subject matter expertise with analytical technology.

Education & Experience Requirements:
Education:
  • Bachelor of Science (BS) in Biological Sciences, Chemistry, Biochemistry or a relevant discipline is required.
  • Master of Science (MS) in Biological Sciences, Chemistry, Biochemistry or a relevant discipline is preferred.
  • PhD in Biological Sciences, Chemistry, Biochemistry or a relevant discipline is preferred.

Experience:
  • A minimum of 4 years of related lab experience with a BS is required.
  • A minimum of 2 years of related lab experience with a MS is required.
  • Experience in Chemical/Biochemical testing is required.
  • Experience in a regulated environment (FDA, EPA, etc.) is required.
  • Knowledge of FDA and cGMP requirements are required.

Compliance Requirements:
The minimum compliance expectation for this role entails strict adherence to FDA regulations and company policies governing sales and marketing activities. This includes completion of required compliance training, accurate documentation of sales interactions, and adherence to data privacy regulations. Additionally, the role requires proactive participation in compliance reviews, prompt reporting of any potential issues, and ongoing education to stay updated on relevant FDA regulations.
Job Description Footer:
In addition to competitive compensation, we offer a comprehensive benefits package including:
  • 401K plan with employer match and immediate vesting
  • Medical, Vision, Life and Dental Insurance
  • Pet Insurance
  • Company paid STD and LTD
  • Company Paid Holidays
  • 3 Weeks' Paid Time Off (within the first year)
  • Tuition Assistance (after the first year)Easily accessible to Tri-Rail
  • Free shuttle to the Boca Tri-Rail station

ADMA Biologics uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit www.dhs.gov/E-Verify.
ADMA Biologics is an Equal Opportunity Employer.

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