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Fda Scientist Jobs in Florida (NOW HIRING)

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 ...

Sr. Sterilization Scientist

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 ...

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 ...

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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$37.7K

$83.2K

$102.8K

How much do fda scientist jobs pay per year?

As of Aug 29, 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 job categories do people searching Fda Scientist jobs in Florida look for?

The top searched job categories for 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.

Senior Formulation Scientist and Quality Assurance

Medical Group Care

Naples, FL • On-site

Full-time

Medical, Retirement, PTO

Re-posted 28 days ago


Job description

Benefits:
  • 401(k) matching
  • Bonus based on performance
  • Health insurance
  • Paid time off

About the Role
We are seeking a highly skilled and experienced Senior Formulation & Quality Assurance
Scientist to join our growing team. In this dual-focus role, you will be responsible for developing innovative,
safe, and effective formulations across FDA-regulated categories in cosmetics and health while ensuring that all products meet rigorous quality, regulatory, and
safety standards. The ideal candidate brings a deep passion for cosmetic science, a sharp analytical mindset,
and a proven track record in both the lab and in quality systems.
Key Responsibilities
Ideation, Strategy & Market Opportunity
-
lead white space research and competitive landscape analysis to identify consumer needs and market share growth opportunities across cosmetics, OTC, and medical device categories to grow (own merit) category for both retail and cobtorl brands.
- benchmark formulations, claims, performance, and cost structures against national brands and category leaders to infomr innovation and positioning strategies.
translate cosnumer insights, clinical needs, and regulatory constraints into clear technical and commercialization roadmaps. 
Product Formulation & Technical Ownership
- own the development and formulation specifications as the subject-matter-expert (SME)
- design, develop, and optimize skincare formulations across Cosmetic skincare and personal care assortments, OTC drug products (e.g. acne, dandruff, skin protectants, suncreens, cold/cough remedies, digestive health) and Medical devices and combination products, where applicable
- take full ownership of formulations, including composition, processing parameters, stabilty, performance, and cost optimization.
- source and evaluate raw materials and active ingredients in collaboration with key stakeholders and maintain clear communication in driving cost-effective startegy(ies) while maintaining competitive in market share.
- guide and parter with contract manufacturers (co-mans) and their technical teams, providing direction on formulation refinement, process optimization, and scale-up readiness.
- lead formulation advacement from bench prototype >>pilot >> full-scale commercial production, resolving scale-related challenges proactively.
- evaluate, qualify, and approve rwa materials, actives, excipients, and packaging components in alignments with regulatory and quality requirements.
- conduct and interpret stability, compatibility, and efficacy testing to validate new formulations.
- stay current with emerging ingredients, technologies, and consumer trends to drive product innovation.
- work cross-functionally with marketing, packaging, and regulatory teams to bring products from concept
to commercialization.
Commercilization & Scale-Up
- own technical readiness for launch, nsuring formulations are robust, reproducible, and commercially viable.
- support road map transfer to manufacturing sites, processing instructions and specifications, and critical quality attributes.
- ensure seamless collaborationacross to meet launch timelines.
- identify and mitigate technical, quality, and regulatory risks prior to commercialization.
Quality Assurance
- maintain data-driven  quality management systems (QMS) in accordance with GMP, relevant ISO standardsand regulatory frameworks.
- develop and implement streamlined, standardized processes across contract manufacturing parters to improve operational efficiency, reduce cycle times, and ensure consistent, on-time delivery of development and commercialization milestones.
- establish and oversee SOPs for raw material testing, in-process checks, and finished product release.
- investigate and resolve product quality complaints, non-conformances, and deviations using root cause
analysis (e.g., CAPA, 8D).
- ensure all products comply with applicable cosmetic regulations (FDA, EU Cosmetics Regulation, or relevant regional standards).
- maintain and review safety data sheets (SDS), product safety assessments, and documentation for
regulatory submissions.
Qualifications
Education
Bachelor's degree (minimum) in Cosmetic Science, Chemistry, Biochemistry, Pharmaceutical Sciences,
or a related field.
Master's degree or PhD is a strong advantage.
Experience
5+ years of hands-on experience in skincare product formulation.
5+ years of experience in a quality assurance or regulatory compliance role within the cosmetics or
personal care industry.
Demonstrated experience working with a wide range of cosmetic raw materials, emulsion systems,
actives, and preservative systems.
Language: English and Chinese 
Skills & Knowledge
Deep knowledge of cosmetic chemistry, skin biology, and ingredient interactions.
Proficiency with formulation software and laboratory equipment (rheometers, pH meters,
spectrophotometers, etc.).
Strong understanding of global cosmetic regulatory requirements (FDA 21 CFR, EU No. 1223/2009, ISO
22716, etc.).
Experience with stability testing protocols (ICH guidelines or equivalent).
Excellent analytical, problem-solving, and documentation skills.
Strong project management and cross-functional collaboration abilities.
Familiarity with ERP and QMS software is a plus.
Soft Skills & Leadership Competencies
- self-starter with high initiative; thrives in fast-paced, ambiguous environments
- innovative and forward-thinking mindset, with ability to seek forward towards continuous improvement.
- results-oriented problem solver who delivers practical, scalable solutions.
- strong ownership mentality with accountability of outcomes.
- effective communicator capable of influencing without authority.
- able to work independently while collaborating seamlessly across teams. 

Medical Group Care logo

About Medical Group Care

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

11 - 50 Employees

Headquarters location

Naples, FL, US

Year founded

2009