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Fda Jobs (NOW HIRING)

The Rockridge Group

FDA Attorney

Pine Brook, NJ · On-site +1

TITLE: FDA ATTORNEY POSITIION: DIRECT HIRE Firm X, established in 2000, is a national boutique law firm focused exclusively on Healthcare and Life Sciences. The Firm draws on its experience ...

Foxstone Recruiting

FDA Partner

Washington, DC · On-site

FDA: Pharmacy & Life Sciences Partner United States * National Practice A prestigious AmLaw firm is seeking an FDA: Pharmacy & Life Sciences Partner to join its growing national practice. Expanding ...

Jobot

Senior FDA Attorney

Pine Brook, NJ · On-site +1

$250K - $400K/yr

The firm maintains a highly active FDA practice and receives an average of approximately five new FDA-related client inquiries each week. The successful candidate will inherit access to a strong ...

Airgas

FDA Compliance Specialist

Independence, OH · On-site

$71 - $106/hr

R10095760 FDA Compliance Specialist (Open) Location: Independence, OH - Rockside Woods Blvd - Management - North BSCHorsham, PA (Regional Office) - Management, Waterford, CT (Regional Office ...

Airgas

FDA Compliance Specialist

Independence, OH · On-site

$71K/yr

R10095760 FDA Compliance Specialist (Open) Location: Independence, OH - Rockside Woods Blvd - Management - North BSCHorsham, PA (Regional Office) - Management, Waterford, CT (Regional Office ...

Airliquidehr

FDA Compliance Specialist

Waterford, CT · On-site

$10K/mo

R10095760 FDA Compliance Specialist (Open) Location: Independence, OH - Rockside Woods Blvd - Management - North BSCHorsham, PA (Regional Office) - Management, Waterford, CT (Regional Office ...

Airgas

$71 - $106/hr

R10095760 FDA Compliance Specialist (Open) Location: Independence, OH - Rockside Woods Blvd - Management - North BSCHorsham, PA (Regional Office) - Management, Waterford, CT (Regional Office ...

UNC-Chapel Hill

FDA IND-IDE Specialist

Chapel Hill, NC · On-site

$30/hr

Position Summary The temporary FDA IND/IDE Specialist is responsible for the organization, coordination, review, and submission of regulatory documents supporting Investigational New Drug (IND ...

Airgas

FDA Compliance Specialist

Independence, OH · On-site

$10K/mo

R10095760 FDA Compliance Specialist (Open) Location: Independence, OH - Rockside Woods Blvd - Management - North BSCHorsham, PA (Regional Office) - Management, Waterford, CT (Regional Office ...

Alston

FDA Technical Consultant

Washington, DC · On-site +1

Alston & Bird is seeking an experienced FDA consultant to work with the Health Care team's FDA practice out of the Washington, D.C. Office. Qualified candidates will have at least 5 years' experience ...

Airgas

FDA Compliance Specialist

Independence, OH · On-site

$71K/yr

R10095760 FDA Compliance Specialist (Open) Location: Independence, OH - Rockside Woods Blvd - Management - North BSCHorsham, PA (Regional Office) - Management, Waterford, CT (Regional Office ...

Alston & Bird's

FDA Technical Consultant

Washington, DC · On-site

Alston & Bird is seeking an experienced FDA consultant to work with the Health Care team's FDA practice out of the Washington, D.C. Office. Qualified candidates will have at least 5 years' experience ...

Airliquidehr

FDA Compliance Specialist

Horsham, PA · On-site

$10K/mo

R10095760 FDA Compliance Specialist (Open) Location: Independence, OH - Rockside Woods Blvd - Management - North BSCHorsham, PA (Regional Office) - Management, Waterford, CT (Regional Office ...

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Fda information

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How much do fda jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for fda in the United States is $39.35, according to ZipRecruiter salary data. Most workers in this role earn between $24.52 and $49.04 per hour, depending on experience, location, and employer.

What does an FDA professional do?

An FDA professional works for the U.S. Food and Drug Administration, a federal agency responsible for protecting public health by ensuring the safety and efficacy of drugs, medical devices, food, cosmetics, and other products. Their roles can include reviewing and approving new drugs and medical devices, conducting inspections, enforcing regulations, and providing guidance to industries. FDA professionals may also work in research, policy development, and public outreach to ensure that products meet regulatory standards and are safe for consumer use.

What are the key skills and qualifications needed to thrive as an FDA Regulatory Affairs Specialist, and why are they important?

To thrive as an FDA Regulatory Affairs Specialist, you need a strong background in life sciences, regulatory guidelines, and compliance, usually supported by a relevant degree such as pharmacy, biology, or chemistry. Familiarity with regulatory submission systems, FDA regulations (such as 21 CFR), and certifications like RAC (Regulatory Affairs Certification) are highly beneficial. Attention to detail, strong analytical thinking, and effective communication skills help professionals navigate complex regulations and collaborate with cross-functional teams. These competencies ensure that products meet legal requirements and safety standards, facilitating successful approvals and market access.

What are some typical challenges faced by professionals working at the FDA, and how can they be managed?

Professionals at the FDA often navigate complex regulatory requirements, tight deadlines, and the need to balance public health priorities with industry innovation. Collaborating across multidisciplinary teams and staying updated on evolving scientific data are essential parts of the role. Adapting to frequent changes in policy and handling high volumes of submissions can be demanding, but leveraging strong communication skills and seeking mentorship within the agency can help manage these challenges effectively.

What is the difference between Fda vs Food Scientist?

AspectFdaFood Scientist
Required CredentialsTypically a degree in health, science, or related field; certifications varyBachelor's or master's in food science, microbiology, or related
Work EnvironmentRegulatory agencies, laboratories, inspection sitesFood manufacturing facilities, laboratories, research settings
Employer & Industry UsageU.S. Food and Drug Administration, government agenciesFood companies, research institutions, government agencies
Common Search & Comparison IntentUnderstanding regulatory roles, compliance, and enforcementFood safety, product development, research

While both Fda professionals and Food Scientists work within the food industry, Fda roles focus on regulation, compliance, and enforcement of food safety laws, often within government agencies. Food Scientists primarily engage in research, product development, and ensuring food quality in manufacturing settings. The two careers overlap in food safety knowledge but differ in their primary responsibilities and work environments.

What qualifications do you need to work for the Food and Drug Administration?

To work for the Food and Drug Administration (FDA), candidates typically need a bachelor's degree in a relevant field such as science, engineering, or public health. For certain positions, advanced degrees or specialized certifications may be required, along with relevant work experience and knowledge of regulatory processes and compliance standards.
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Fda jobs near you
Infographic showing various Fda job openings in the United States as of August 2026, with employment types broken down into 77% Full Time, 8% Part Time, and 15% Contract. Highlights an 100% In-person job distribution, with an average salary of $81,844 per year, or $39.3 per hour.

FDA Attorney

The Rockridge Group

Pine Brook, NJ • On-site, Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 14 days ago

Job description

TITLE: FDA ATTORNEY POSITIION: DIRECT HIRE Firm X, established in 2000, is a national boutique law firm focused exclusively on Healthcare and Life Sciences. The Firm draws on its experience representing stakeholders across the entire healthcare spectrum. In the Life Sciences, Firm X, has represented pharmacies of all kinds and assisted with regulatory, transactional, and litigation matters. On the Healthcare side, the Firm's clients have included large physician group practices, hospitals, hospital medical staff, ambulatory surgery centers, laboratory companies, as well as the complete panoply of ancillary service providers. Firm X attorneys are licensed in numerous states. The Firm has offices in Pine Brook, New Jersey, and New York City. A Mid-Level or more senior FDA Attorney (Counsel-level or higher) is sought for Firm X’s Pine Brook, NJ, New York City, or fully remote office. They receive an average of 5 new FDA client inquiries per week. Responsibilities will align with the Attorney’s background, which should include: • Compounding rules, regulations and FDA guidance o 503A o 503B o Bulk API suppliers and repackagers o FDA audits/investigations • Drug supply chain security and track and trace o Trading partner requirements o Unique trading partners (i.e., 3PLs, brokers, etc.) o Serialization implementation requirements o Other drug supply chain considerations • Drug and device manufacturing rules o CGMP compliance o NDA and ANDA filings and evaluation o 510K Premarket Approval Filings and evaluation o OTC filings and evaluation o Advice on manufacturing practices • Clinical trial rules o Structuring and drafting clinical trial agreements, informed consent forms, master service agreements, and related research contracts o Institutional Review Board (IRB) submissions and compliance o Clinical trial design, study initiation, data use, adverse event reporting, and post-trial obligations • Labeling and advertising reviews • FDA registration and annual filings • FDA inspections, 483 responses and warning letters • Drug withdrawals and recalls • FDA importation and exportation rules • Veterinary medicine and veterinary compounding • Dietary supplements • FDA regulated medical devices • Reviews of clinical literature and incorporation into arguments/strategies (access to these clinical literature directories is a plus) Requirements: • 10+ years FDA experience – private law firm experience strongly preferred, but will also consider in-house candidates • Clinical trial experience a plus • Filing copyrights a plus • Filing patents a plus • May work in the Pine Brook or New York City office; will also consider fully remote arrangement if located in other states • Admitted to practice in at least one US state • Experience performing most/all of the job responsibilities of the position (outlined above) • Team-player mindset, and ability to work cohesively and collaboratively with a team of attorneys • Strong work ethic Benefits: Firm X offers a hybrid schedule, competitive salary, and a full range of benefits, including PTO, medical, dental, vision, 401(k) (upon eligibility to participate), on-site gym (Pine Brook), and opportunities for substantial salary progression based on performance and contributions. *The posted salary will depend on years of experience and other factors.