... Quality Assurance Scientist to join our growing team. In this dual-focus role, you will be ... FDA-regulated categories in cosmetics and health while ensuring that all products meet rigorous ...
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... Quality Assurance Scientist to join our growing team. In this dual-focus role, you will be ... FDA-regulated categories in cosmetics and health while ensuring that all products meet rigorous ...
Quick apply
... Quality Assurance Scientist to join our growing team. In this dual-focus role, you will be ... FDA-regulated categories in cosmetics and health while ensuring that all products meet rigorous ...
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 ...
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 ...
He/she would be responsible for FDA-regulated studies including device and stroke trials and the creation and maintenance of endovascular databases. * The Assistant Scientist will also contribute to ...
He/she would be responsible for FDA-regulated studies including device and stroke trials and the creation and maintenance of endovascular databases. * The Assistant Scientist will also contribute to ...
Miami, FL · On-site
He/she would be responsible for FDA-regulated studies including device and stroke trials and the creation and maintenance of endovascular databases. * The Assistant Scientist will also contribute to ...
Miami, FL · On-site
He/she would be responsible for FDA-regulated studies including device and stroke trials and the creation and maintenance of endovascular databases. * The Assistant Scientist will also contribute to ...
Palm Beach Gardens, FL · On-site
$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 ...
Palm Beach Gardens, FL · On-site
$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 ...
Palm Beach Gardens, FL · On-site
$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 ...
Palm Beach Gardens, FL · On-site
$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 ...
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 ...
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 ...
Biology/Life Science, Agricultural Sciences Department: 60100000 - AG-MICROBIOLOGY - CELL SCI ... and FDA regulations. Work includes, field sampling, extractions and analysis of samples from a ...
Biology/Life Science, Agricultural Sciences Department: 60100000 - AG-MICROBIOLOGY - CELL SCI ... and FDA regulations. Work includes, field sampling, extractions and analysis of samples from a ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
Plantation, FL · On-site
Evaluates and selects methods, applies protocols and scientific techniques to accomplish study ... and FDA) * Must have strong analytical skills * Must be a team player and driven individual Must ...
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Plantation, FL · On-site
Evaluates and selects methods, applies protocols and scientific techniques to accomplish study ... and FDA) * Must have strong analytical skills * Must be a team player and driven individual Must ...
... FDA and global regulatory authorities • Ensure compliance with GxP, 21 CFR Part 11, HIPAA, and ... Computer Science, Statistics, Life Sciences, or related field • 15+ years of experience in ...
... FDA and global regulatory authorities • Ensure compliance with GxP, 21 CFR Part 11, HIPAA, and ... Computer Science, Statistics, Life Sciences, or related field • 15+ years of experience in ...
... FDA and global regulatory authorities • Ensure compliance with GxP, 21 CFR Part 11, HIPAA, and ... Computer Science, Statistics, Life Sciences, or related field • 15+ years of experience in ...
... FDA and global regulatory authorities • Ensure compliance with GxP, 21 CFR Part 11, HIPAA, and ... Computer Science, Statistics, Life Sciences, or related field • 15+ years of experience in ...
The Scientist II must be well versed in standard principles, theories, concepts and techniques in ... Experience working with CBER (FDA) regulated licensed biologics. The Key Working Relationships ...
The Scientist II must be well versed in standard principles, theories, concepts and techniques in ... Experience working with CBER (FDA) regulated licensed biologics. The Key Working Relationships ...
The Scientist II must be well versed in standard principles, theories, concepts and techniques in ... Experience working with CBER (FDA) regulated licensed biologics. The Key Working Relationships ...
The Scientist II must be well versed in standard principles, theories, concepts and techniques in ... Experience working with CBER (FDA) regulated licensed biologics. The Key Working Relationships ...
The Scientist II must be well versed in standard principles, theories, concepts and techniques in ... Experience working with CBER (FDA) regulated licensed biologics. The Key Working Relationships ...
The Scientist II must be well versed in standard principles, theories, concepts and techniques in ... Experience working with CBER (FDA) regulated licensed biologics. The Key Working Relationships ...
The Scientist II must be well versed in standard principles, theories, concepts and techniques in ... Experience working with CBER (FDA) regulated licensed biologics. The Key Working Relationships ...
The Scientist II must be well versed in standard principles, theories, concepts and techniques in ... Experience working with CBER (FDA) regulated licensed biologics. The Key Working Relationships ...
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 ...
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 ...
$37.7K - $43.6K
2% of jobs
$43.6K - $49.6K
0% of jobs
$49.6K - $55.5K
5% of jobs
$55.5K - $61.4K
0% of jobs
$61.4K - $67.3K
1% of jobs
$69.6K is the 25th percentile. Wages below this are outliers.
$67.3K - $73.2K
42% of jobs
$73.2K - $79.1K
1% of jobs
$79.1K - $85K
1% of jobs
$85K - $90.9K
19% of jobs
$90.9K - $96.8K
0% of jobs
$97.5K is the 75th percentile. Wages above this are outliers.
$96.8K - $102.8K
28% of jobs
$37.7K
$83.2K
$102.8K
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.
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.
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.
The most popular types of Fda Scientist jobs in Florida are:
For Fda Scientist jobs in Florida, the most frequently searched job titles are:
The top searched job categories for Fda Scientist jobs in Florida are:

Full-time
Medical, Retirement, PTO
Re-posted 28 days ago
Sourced by ZipRecruiter
Medical equipment and supplies manufacturing
11 - 50 Employees
Naples, FL, US
2009