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Fda Attorney Jobs (NOW HIRING)

The Rockridge Group

FDA Attorney

Pine Brook, NJ · On-site +1

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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 ...

Jobot

Senior FDA Attorney

Pine Brook, NJ · On-site +1

$250K - $400K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Salary: $250,000 - $400,000 per year A bit about us: ----- Senior FDA Attorney Counsel or Senior Counsel | New Jersey, New York or Fully Remote A nationally recognized boutique law firm focused ...

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 ... Key Responsibilities * Assist attorneys in supporting manufacturing clients on issues related to ...

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 ...

NxT Level

Associate, FDA Regulations - DC

Washington, DC · On-site

$365K/yr

  • PTO

This is an outstanding opportunity for a motivated attorney to advise a diverse range of clients across the FDA-regulated product ecosystem, including pharmaceuticals, medical devices, biologics ...

Robert Half

Attorney/Lawyer

Manhattan, NY · On-site

$104.50 - $121/hr

This role is ideal for an attorney who thrives in fast-paced, collaborative environments and has ... Advise on regulatory considerations impacting purchasing, including HIPAA, FDA compliance, CMS ...

K2 Ascend

Healthcare Attorney

Detroit, MI

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Healthcare Attorney Location: Detroit, Troy, Ann Arbor, Lansing, or Grand Rapids Type: Full-Time, ... FDA regulations, Michigan Public Health Code, and Michigan Mental Health Code * Counsel healthcare ...

Axiom Talent Platform

Life Sciences Attorney (Remote)

OR · On-site +1

$309K/yr

  • Medical

  • Dental

  • Vision

  • PTO

We are seeking both experienced Promotional Review lawyers and Market Access lawyers who have at ... with FDA, FTC and other applicable regulations. * Work closely with cross-functional teams ...

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All JobsFda Attorney Jobs

Fda Attorney information

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$46K

$108.2K

$172.5K

How much do fda attorney jobs pay per year?

As of Aug 16, 2026, the average yearly pay for fda attorney in the United States is $108,160.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,000.00 and $130,000.00 per year, depending on experience, location, and employer.

What are some common challenges faced by FDA attorneys when working with clients in highly regulated industries?

FDA attorneys often encounter challenges related to the complexity and frequent changes of regulations governing pharmaceuticals, medical devices, food, and cosmetics. Clients may struggle to interpret and implement new compliance requirements, and attorneys must provide clear guidance while staying up to date with evolving laws and FDA guidance documents. Additionally, FDA attorneys frequently collaborate with regulatory affairs, quality assurance, and product development teams to ensure clients' products meet both legal and scientific standards. Managing tight deadlines for submissions and responding to enforcement actions or warning letters can also be a significant part of the role.

What is the difference between Fda Attorney vs Regulatory Affairs Specialist?

AspectFda AttorneyRegulatory Affairs Specialist
Required CredentialsJuris Doctor (JD), Bar Admission, often specialized in healthcare or FDA lawBachelor's or Master's in life sciences, regulatory affairs, or related fields; certifications like RAC
Work EnvironmentLegal firms, in-house legal departments, government agenciesPharmaceutical, biotech companies, healthcare organizations
Industry UsageLegal compliance, FDA regulations, legal advisingProduct registration, compliance, regulatory strategy

Fda Attorneys focus on legal aspects of FDA regulations, providing legal advice and ensuring compliance through legal channels. Regulatory Affairs Specialists handle the practical aspects of regulatory submissions and compliance strategies within organizations. While both roles require knowledge of FDA regulations, Fda Attorneys emphasize legal interpretation and advocacy, whereas Regulatory Affairs Specialists focus on operational compliance and product approval processes.

What is an FDA attorney?

FDA attorneys are legal professionals who specialize in laws and regulations enforced by the U.S. Food and Drug Administration (FDA). They advise companies in the pharmaceutical, food, medical device, and biotechnology industries on how to comply with FDA rules. Their work includes helping with product approvals, labeling, advertising, clinical trials, and responding to FDA enforcement actions. FDA attorneys also represent clients in disputes with the agency and may assist with policy development or regulatory strategy.

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

To thrive as an FDA Attorney, you need a law degree, active bar membership, and deep knowledge of FDA regulations, healthcare law, and compliance practices. Familiarity with regulatory submission systems, legal research databases, and document management tools like LexisNexis and Westlaw is typical. Strong analytical thinking, negotiation skills, and the ability to communicate complex legal concepts clearly are crucial soft skills. These qualifications ensure effective client representation, regulatory compliance, and successful navigation of the complex life sciences legal environment.
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Cities with the most Fda Attorney job openings:

What states have the most Fda Attorney jobs?

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Fda Attorney jobs near you
Infographic showing various Fda Attorney job openings in the United States as of August 2026, with employment types broken down into 94% Full Time, 5% Part Time, and 1% Contract. Highlights an 78% Physical, 12% Hybrid, and 10% Remote job distribution, with an average salary of $108,160 per year, or $52 per hour.

FDA Attorney

The Rockridge Group

Pine Brook, NJ • On-site, Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 24 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.