Non-Equity Partner — FDA & Regulatory Law

The FDA Law Solution; Atlanta (GA); Hybride; USD 350 000 - 600 000; Plein temps

Résumé du poste

The FDA Law Solution, LLC seeks a Non-Equity Partner in Atlanta, GA to lead FDA and regulatory matters, manage high-level client relationships, and own a portable practice bridging FDA rules with business innovation. This on-site, full-time role reports to the Founder & CEO in a boutique firm.

The ideal candidate has 15+ years of specialized FDA or state regulatory experience, with expertise in Medical Devices or Food and Dietary Supplements, and a proven ability to develop new business while

Qualifications

• JD from an accredited law school.
• Active bar membership in good standing in one U.S. jurisdiction.
• 15+ years of specialized FDA/regulatory experience.
• Proven ability to manage a portable book of business.
• Expertise in Medical Devices or Food and Dietary Supplements.

Responsabilités

• Navigate FDA regulatory pathways and commercialization strategies for client portfolios.
• Advise on product classification, submissions, labeling, and market expansion.
• Guide clients through inspections, 483 responses, and warning letters.
• Support internal review processes to align with federal standards.
• Develop niche thought leadership and targeted service offerings.

Connaissances

Regulatory strategy

Business development

Client relationship management

Legal compliance

Formation

Juris Doctor (JD) degree

Active bar membership (US)

Outils

Veeva PromoMats

Description du poste

Non-Equity Partner — FDA & Regulatory Law

Atlanta, GA (On-Site) Full-time Reports to: Founder & CEO

We are seeking an entrepreneurial Non-Equity Partner with over 15 years of experience to navigate complex regulatory matters and own high-level client relationships. The successful candidate will manage a portable practice while providing sophisticated, commercially-grounded legal solutions that bridge the gap between FDA regulations and business innovation. This role is designed for a business-savvy strategist who thrives in a high-stakes, collaborative legal environment.

About the Company

The FDA Law Solution, LLC. is a premier legal advisory firm specializing in navigating the complex regulatory landscape of the Food and Drug Administration. Led by industry veteran Ricky C. Benjamin, the firm provides strategic counsel to life sciences and healthcare companies to ensure product compliance and successful market entry. We operate with a boutique feel where senior expertise is directly accessible, fostering a culture of mentorship, academic rigor, and relentless client dedication.

Regulatory Strategy and Leadership

• Navigate FDA regulatory pathway and commercialization strategies for client portfolios
• Advise on product classification, submissions, labeling, and market expansion
• Guide clients through inspections, 483 responses, and warning letters
• Evaluate litigation exposure involving the Lanham Act and false advertising
• Support internal client review processes to align with federal standards

Business Development and Practice Management

• Maintain and expand a portable book of business through networking
• Develop niche thought leadership and targeted service offerings for clients
• Collaborate on firm-building initiatives and strategic marketing efforts
• Manage billable hour efficiency and minimize realization write-offs
• Identify new business connections that provide entry to target markets

Technical and Promotional Compliance

• Conduct labeling and promotional claims reviews for digital and print
• Audit websites, social media, and paid media for regulatory compliance
• Ensure promotional activity aligns with evolving FDA and FTC standards
• Align scientific data with legal requirements for technical fluency
• Monitor evolving state rules regarding CBD, hemp, and dietary supplements

Required Qualifications

• Juris Doctor (JD) degree from an accredited law school
• Active bar membership in good standing in one U.S. jurisdiction
• 15+ years of specialized FDA or state regulatory experience
• Demonstrated ability to manage a portable book of business
• Proven expertise in Medical Devices or Food and Dietary Supplements

Preferred Qualifications

• Experience with CBD and hemp claim frameworks and state rules
• Knowledge of QSR, ISO 13485, and specific device submission types
• Previous leadership experience within a boutique or specialized regulatory practice
• Familiarity with Veeva PromoMats or similar legal compliance platforms

Standard weekday hours with fluctuations based on client and trial demands

Hybrid work arrangement with a preferred presence in the Atlanta office

Occasional travel required for client inspections, audits, or industry conferences

Collaborative environment requiring frequent interaction with the Founder and CEO

Salary & Benefits

Competitive salary and benefits package depending on candidate's experience.

Culture & Expectations

• Demonstrate high-level strategic thinking and solution-oriented mindsets
• Maintain self-motivation and the ability to operate independently
• Exhibit professional respect and alignment with firm leadership
• Show technical and scientific fluency in all client interactions

Growth & Development

This position offers a significant platform for a senior attorney to scale and develop a niche practice line, such as Devices or Supplements. The firm provides full support for thought leaders looking to expand their personal brand and professional reach. Exceptional performers who demonstrate long-term commitment and strategic value may be considered for a path toward equity partnership and further leadership responsibilities.

Ready to Apply?

Interested candidates should submit a resume and cover letter, along with a summary of their portable practice or representative matters.