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Fda Regulatory Attorney Jobs (NOW HIRING)

Vesync

Senior Product Counsel - Health

Tustin, CA

$160K/yr

Preferred Qualifications * 7+ years of legal experience as a practicing attorney, including at a law firm, in-house, or in government. * Deep understanding of the FTC and FDA regulatory framework for ...

Vesync

Senior Product Counsel - Health

Tustin, CA

$160K/yr

Preferred Qualifications * 7+ years of legal experience as a practicing attorney, including at a law firm, in-house, or in government. * Deep understanding of the FTC and FDA regulatory framework for ...

Vesync

Senior Product Counsel - Health

Tustin, CA · On-site

$160K/yr

Preferred Qualifications * 7+ years of legal experience as a practicing attorney, including at a law firm, in-house, or in government. * Deep understanding of the FTC and FDA regulatory framework for ...

BoehringerPRD

Director & SR Counsel II

Johns Creek, GA · On-site

... g., patents, FDA Regulatory, commercial, litigation, etc.) critical to maintaining business ... The position holder mentors more junior attorneys in areas of expertise. Duties & Responsibilities

Abbott

Senior Counsel, Regulatory

Chicago, IL · On-site

$143K - $195K/yr

Responsible for counseling on FDA and state laws, regulations, and guidance documents with respect ... attorneys. Required Qualifications * Juris Doctor degree from an accredited law school; strong ...

Trustpoint.One

Compliance Attorney

Carlsbad, CA · On-site

FDA promotional regulations and healthcare compliance laws and regulations. * Excellent ... attorney with pharmaceutical industry experience and a passion for providing practical business ...

Abbott

Senior Counsel, Regulatory

Washington, DC · On-site

$158K - $214K/yr

Responsible for counseling on FDA and state laws, regulations, and guidance documents with respect ... attorneys. Required Qualifications * Juris Doctor degree from an accredited law school; strong ...

Abbott

Senior Counsel, Regulatory

Chicago, IL

$143K - $195K/yr

Responsible for counseling on FDA and state laws, regulations, and guidance documents with respect ... attorneys. Required Qualifications * Juris Doctor degree from an accredited law school; strong ...

Abbott

Senior Counsel, Regulatory

Washington, DC

$158K - $214K/yr

Responsible for counseling on FDA and state laws, regulations, and guidance documents with respect ... attorneys. Required Qualifications * Juris Doctor degree from an accredited law school; strong ...

Merck Group

Senior Counsel -US Rare Tumors

Boston, MA · On-site

$188K - $283K/yr

Serve as lead attorney for a key brand of the Rare Tumors Therapeutic area, including: review of ... Compliance & Regulatory Oversight: Ensure all activities comply with FDA, OIG, CMS, and state ...

5 Legal

Healthcare Regulatory Associate

Austin, TX

Our team seeks to add a dynamic lawyer with good verbal and written skills to assist in healthcare ... of FDA-regulated products. Ideal candidates will have demonstrated experience in healthcare ...

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Fda Regulatory Attorney information

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$69K

$137.4K

$199K

How much do fda regulatory attorney jobs pay per year?

As of Aug 10, 2026, the average yearly pay for fda regulatory attorney in the United States is $137,408.00, according to ZipRecruiter salary data. Most workers in this role earn between $100,000.00 and $166,000.00 per year, depending on experience, location, and employer.

What are some typical daily responsibilities of an FDA Regulatory Attorney?

As an FDA Regulatory Attorney, your daily responsibilities often include advising clients or internal teams on regulatory compliance, preparing and reviewing submissions to the FDA, and interpreting new or updated regulations. You may also collaborate closely with scientists, quality assurance professionals, and business leaders to assess risks and develop strategies for product approvals or compliance matters. Regular activities can involve drafting legal documents, managing responses to agency inquiries, and staying updated on recent FDA guidance. The role is dynamic and requires coordinating across different departments and occasionally negotiating with regulatory authorities.

What are the key skills and qualifications needed to thrive as an FDA Regulatory Attorney?

To thrive as an FDA Regulatory Attorney, you need a strong background in law with experience in FDA regulations, compliance, and life sciences, typically supported by a JD degree and state bar admission. Familiarity with regulatory submission systems, research databases, and knowledge of electronic document management tools are important technical assets. Outstanding attention to detail, problem-solving abilities, and persuasive communication skills set top candidates apart. These competencies are crucial for navigating complex regulatory processes, advising clients, and ensuring legal compliance in highly regulated industries.

What does an FDA Regulatory Attorney do?

An FDA Regulatory Attorney advises clients on compliance with regulations set by the U.S. Food and Drug Administration (FDA). They assist companies in industries such as pharmaceuticals, medical devices, food, and cosmetics to navigate regulatory approvals, labeling requirements, and enforcement actions. Their work often involves reviewing submissions to the FDA, handling inspections, and ensuring products meet legal requirements. They may also represent clients in litigation or administrative proceedings related to FDA regulations.

More about Fda Regulatory Attorney jobs
What cities are hiring for Fda Regulatory Attorney jobs? Cities with the most Fda Regulatory Attorney job openings:
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Fda Regulatory Attorney jobs near you
Infographic showing various Fda Regulatory Attorney job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 87% Full Time, 9% Part Time, and 3% Contract. Highlights an 90% Physical, 4% Hybrid, and 6% Remote job distribution, with an average salary of $137,408 per year, or $66.1 per hour.

Associate General Counsel, R&D Innovation Legal

AbbVie

Washington, DC • On-site

$182K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 2 days ago

AbbVie rating

8.6

Company rating: 8.6 out of 10

Based on 101 frontline employees who took The Breakroom Quiz

16th of 86 rated pharmaceutical

Job description

Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
As an Associate General Counsel in the R&D Innovation Legal group, you will support AbbVie's R&D organization in navigating enterprise-critical issues in an evolving legal and regulatory environment as we work to bring new, innovative products to patients. This individual will be motivated by the opportunity to address and solve emerging issues with a strategic and creative business-oriented approach and provide expert counsel on decisions impacting our long-term pipeline strategies.
Key Responsibilities
Develop and provide strategic counsel to senior leaders within the Legal and Regulatory Strategy organizations on legal regulatory issues that impact pipeline development and product innovation. Assigned matters have significant impact to AbbVie overall. This is a role advising the R&D organization and not on FDA promotional considerations or advising the Commercial organization.
Provides legal support to Regulatory Affairs on critical and strategic regulatory filings and agency engagements relating to R&D issues impacting our investigational and on-market drug products.
Willing to develop an understanding of the Inflation Reduction Act and other "Most Favored Nation" policies to provide strategic counsel to the R&D organization.
Educates other AbbVie legal departments and business stakeholders on emerging laws, regulations and industry trends impacting AbbVie portfolio.
Proactively identifies highly complex legal issues related to assigned matters, develops creative and alternative solutions, and implements resolution.
Adopts a business oriented and creative approach to problem solving.
Identifies unmet needs and future legal issues and proactively proposes strategies to optimize outcomes and results for the company.
Advises Vice Presidents, Presidents and Officers. Recognized by these clients as both expert in substantive area and relied upon for individual advice.
To be successful in this role:
  • You offer specialized FDA regulatory and drug development experience.

You have demonstrated success in providing strategic counsel to leaders within the pharmaceutical industry.
Qualifications
  • J.D. and currently admitted to the bar in at least one U.S. state.
  • Minimum of 10+ years (12+ preferred) of relevant experience practicing as a member of a nationally recognized law firm in a life sciences practice, practicing in-house at a pharmaceutical company or practicing as an attorney for the FDA, or any combination of the above (experience working in-house or at FDA is preferred).
  • Individual will have substantial expertise in FDA regulations and guidance around innovator drug development, including on regulatory exclusivities, orphan drug designations, clinical trial design and data requirements and combination products, and have familiarity with policies to advance innovation in the industry.
  • Experience working for, or having interactions with, government health authorities is highly desirable.
  • Familiarity with the Inflation Reduction Act, Most Favored Nation and CMS policies and their impact on drug development strategies is a plus.
  • Knowledge and understanding of pharmaceutical laws and regulations to help business clients assess issues in a highly regulated landscape.
  • Demonstrated ability to work independently and lead cross-functional teams collaboratively.
  • Ability to adapt to a changing environment while handling multiple priorities.
  • Excellent oral and written communication skills. Comfortable presenting complicated information accurately and concisely to senior leaders.
  • To enable success in the role, an individual must be able to be in the office 3 days/week at our offices in North Chicago, IL or the Washington, DC metro area.

Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this postingbased on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more orless than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our short-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paidand may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html

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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013

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