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Fda Scientist Jobs in Florida (NOW HIRING)

... FDA) and other global regulatory agencies. Job-Specific Responsibilities / Functions * Design and execute studies related to pre-formulation and formulation of parenteral products, including ...

General Responsibilities A Research Scientist conducts advanced studies in a specific field ... FDA requirements. * Maintains cGMP compliance for cyclotron facility operations. * Follows site ...

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 ...

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 ...

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 ...

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 ...

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 ...

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Showing results 1-20

Fda Scientist information

See Florida salary details

$37.7K

$83.2K

$102.8K

How much do fda scientist jobs pay per year?

As of Sep 5, 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:

Infographic showing various Fda Scientist job openings in Florida as of August 2026, with employment types broken down into 82% Full Time, 15% Part Time, 2% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $83,206 per year, or $40 per hour.

Associate Scientist & Scientist - Pharmaceutical Industry

ttg Talent Solutions

Coral Springs, FL

Other

Posted 5 days ago


Job description

Associate Scientist & Scientist
Location: Coral Springs, FL 33065
Type of Work: On-Site
Schedule: 1st Shift & 2nd Shift
Type of Contract: Temp-to-Perm
Department: Research & Development - Analytical & Formulation
 
About the Opportunity
A fast-growing pharmaceutical research and manufacturing organization is expanding its R&D operations in Coral Springs, FL. We are seeking motivated Scientists and Associate Scientists (Levels I & II) to support formulation and analytical development for inhalation-based drug products, including MDI, DPI, and nasal spray formulations.
These are hands-on laboratory roles in a GMP-regulated environment. Successful candidates will demonstrate strong documentation skills (GDP), attention to detail, and the ability to perform and review analytical work with minimal supervision.
This is an excellent opportunity to be involved in pre-formulation, formulation, analytical method development, data interpretation, troubleshooting, and continuous improvement initiatives.
 
Key Responsibilities
  • Perform routine and advanced analytical testing of raw materials, in-process, and finished products in compliance with GMP.
  • Support the development of formulations (solutions, suspensions, propellant-based systems) for inhalation drug products.
  • Operate and troubleshoot analytical instruments including HPLC, UPLC, GC, UV, and FTIR, and manage data through Empower (Waters) software.
  • Prepare and review protocols, reports, and SOPs in alignment with quality and regulatory requirements.
  • Ensure all documentation complies with Good Documentation Practices (GDP) and data integrity standards.
  • Participate in method transfer, verification, and validation activities as assigned.
  • Support investigations of OOS/OOT, deviations, and CAPA with accurate analytical input.
  • Collaborate cross-functionally during manufacturing trials and scale-up activities.
  • Mentor junior scientists and contribute to the team's technical development.
  • Maintain a safe and compliant laboratory environment in accordance with EH&S and corporate policies.
Qualifications
  • PhD, MS, or BS in Analytical Chemistry, Pharmaceutics, Pharmaceutical Sciences, Biochemistry, or related discipline.
  • Minimum 1 year of hands-on GMP laboratory experience (academic-only exposure will not be considered).
  • Proven hands-on experience with chromatographic systems (HPLC, UPLC, GC) and analytical testing.
  • Working knowledge of GMP/GLP, USP, ICH, and FDA regulatory expectations.
  • Experience with Empower software for data acquisition and reporting strongly preferred.
  • Solid understanding of GDP  and deviation processes.
 
Preferred Attributes
  • Prior exposure to regulated audits (FDA, EMA, MHRA) is advantageous.
  • Experience in method validation or transfer projects a plus.
  • Strong analytical thinking, data review, and problem-solving skills.
  • Excellent communication and teamwork abilities.
  • High attention to detail, organization, and quality compliance.
 
ttg Talent Solutions is an Equal Opportunity Employer and recruiting agency. We are committed to creating an inclusive and diverse work environment and welcome applications from all qualified candidates regardless of race, color, religion, gender, sexual orientation, national origin, age, disability, or veteran status. Please note that all offers of employment are contingent upon the successful completion of a drug test and background check. We maintain a drug- and substance-free workplace to ensure the safety and well-being of all employees.
 
At ttg, 'We believe in making a difference One Person at a Time,' ttg OPT.
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