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Fda Scientist Jobs (NOW HIRING)

The Principal Regulatory Scientist will work closely with client program managers, product ... Demonstrated experience applying FDA regulatory requirements, guidance, and development pathways to ...

Role: Scientist II Location: (Remote but need to report to the duty station in college park, MD or other FDA facilities within DC metropolitan area as per need) : So, look for local candidates.

... FDA, EMA, and global regulatory expectations. Success requires exceptional analytical acumen ... Bachelor's of Science (or higher) in Chemistry or other related field * 7+ years experience in ...

The Staff Scientist mentors junior scientists, serves as a subject matter expert, and plays a ... IVDD, IVDR, FDA 21 CFR 800 series, FDA 21 CFR Part 11) * Note: these requirements do not apply for ...

Scientist Group Leader

Devens, MA ยท On-site

$84K - $94K/yr

Company Description Eurofins Scientific is an international life sciences company, providing a ... Responsible for contributing to audit readiness and for participating in quality audits with FDA ...

The Staff Scientist mentors junior scientists, serves as a subject matter expert, and plays a ... IVDD, IVDR, FDA 21 CFR 800 series, FDA 21 CFR Part 11) * Note: these requirements do not apply for ...

The Staff Scientist mentors junior scientists, serves as a subject matter expert, and plays a ... IVDD, IVDR, FDA 21 CFR 800 series, FDA 21 CFR Part 11) * Note: these requirements do not apply for ...

Bering-Alaka`ina Holdings, LLC is looking for Scientist to perform services that impact a Combat ... Experience with in vitro testing of pharmaceuticals for FDA approval. * Experience developing high ...

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Fda Scientist information

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$50.5K

$111.3K

$137.5K

How much do fda scientist jobs pay per year?

As of Aug 17, 2026, the average yearly pay for fda scientist in the United States is $111,343.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,500.00 and $137,000.00 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.

Does the FDA employ scientists?

Yes, the FDA employs scientists in various roles such as biologists, chemists, and pharmacologists to evaluate the safety and effectiveness of medical products, foods, and cosmetics. These scientists often work in laboratories, conduct research, and analyze data to support regulatory decisions, typically requiring relevant degrees and certifications. Their work is essential to ensuring public health and safety standards are met.

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 over $120,000. Salaries may also include benefits such as health insurance and retirement plans.
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What cities are hiring for Fda Scientist jobs?

Cities with the most Fda Scientist job openings:

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

The most popular types of Fda Scientist jobs are:

What states have the most Fda Scientist jobs?

States with the most job openings for Fda Scientist jobs include:

Infographic showing various Fda Scientist job openings in the United States as of August 2026, with employment types broken down into 81% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $111,343 per year, or $53.5 per hour.

Regulatory Affairs Specialist (FDA, DEA )

Barupon LLC

Irvine, CA โ€ข On-site

$60K - $76K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 10 days ago


Job description

Job Summary
The Regulatory Affairs Specialist (FDA, DEA) will ensure BaRupOn's pharmacy, manufacturing, and healthcare operations meet all applicable regulatory requirements. This position is responsible for preparing submissions, maintaining licenses, coordinating audits, and staying ahead of evolving federal and state regulations related to pharmaceuticals, medical devices, and controlled substances.
Key Responsibilities
  • Prepare and manage FDA submissions (e.g., drug listings, establishment registrations, 503A/503B updates)
  • Oversee and renew DEA registrations, inventory records, and security documentation
  • Maintain state pharmacy, medical device, and wholesale distribution licenses
  • Track regulatory changes affecting compounding, controlled substances, and labeling requirements
  • Support internal audits, site inspections, and responses to 483s or warning letters
  • Coordinate with Quality Assurance on SOP compliance, change controls, and deviation reports
  • Serve as point of contact with federal and state regulatory agencies
  • Document and file compliance records and ensure timely reporting
Qualifications
  • Associate degree in Life Sciences, Regulatory Affairs, or related field (Bachelor's preferred)
  • 2-4 years of regulatory or compliance experience in pharmaceuticals, biotech, or medical devices
  • Working knowledge of FDA regulations (21 CFR Parts 210, 211, 820) and DEA requirements
  • Strong writing, documentation, and organizational skills
  • Familiarity with electronic submission systems, labeling requirements, and drug master files
Preferred Skills
  • Experience in sterile or non-sterile compounding (503A or 503B environments)
  • Knowledge of NABP license portals, MedWatch reporting, or REMS programs
  • Regulatory Affairs Certification (RAC) or DEA compliance training (preferred)
  • Experience responding to FDA inspections, audits, or state pharmacy board requests
Benefits
  • Health, dental, and vision insurance
  • 401(k) with employer match
  • Paid time off and holidays
  • Regulatory training and continuing education support
  • Advancement opportunities into QA/RA leadership roles