NON-EQUITY PARTNER
Non-Equity Partner — FDA & Regulatory LawLocation: Atlanta, GA (On-Site)Employment Type: Full-timeReports To: Founder & CEOAbout the CompanyThe 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 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.Position SummaryWe 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.Core ResponsibilitiesRegulatory Strategy and LeadershipThe Non-Equity Partner serves as a primary architect for client regulatory pathways. You will navigate the development of commercialization strategies for diverse medical device or food and supplement portfolios.● 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 standardsBusiness Development and Practice ManagementThis role requires a proactive approach to firm growth and independent practice management. You will be responsible for maintaining a portable book of business that occupies approximately 60% of your capacity.● 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 marketsTechnical and Promotional CompliancePrecision in promotional and technical review is a cornerstone of our firm’s value proposition. You will ensure all client communications meet stringent FDA and FTC standards across all media platforms.● 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 supplementsQualificationsRequired QualificationsCandidates must possess extensive senior-level experience within the FDA regulatory space. We require individuals who demonstrate the intellectual rigor of a major firm background with the agility of a boutique practitioner.● 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 SupplementsPreferred QualificationsThe ideal candidate will bring specialized technical knowledge that complements our existing practice areas. Proficiency with industry-standard compliance tools and emerging regulatory frameworks is highly valued.● 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 platformsWork Environment and Schedule● 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 CEOCompensation and BenefitsSalary and BenefitsCompetitive salary and benefits package depending on candidate's experience.Culture and ExpectationsSuccessful employees at The FDA Law Solution must balance a high-performance work ethic with personal accountability. We value smart, disciplined professionals who respect the firm's established leadership and mission.● 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 interactionsGrowth and Development OpportunitiesThis 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.How to ApplyInterested candidates should submit a resume and a summary of their portable practice or representative matters. A short introduction explaining your interest in a boutique environment should be included. Qualified applicants will be contacted by the Hiring Manager for an initial confidential discussion regarding the next stages of the hiring process.Apply here: https://thefdalawsolution.com/careers/non-equity-partner-fda-regulatory-law