What are the responsibilities and job description for the Non-Equity Partner — FDA & Regulatory Law position at The FDA Law Solution, LLC?
About
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.
Responsibilities
Regulatory Strategy and Leadership
The 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 standards
Responsibilities
Business Development and Practice Management
This 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 markets
Responsibilities
Technical and Promotional Compliance
Precision 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 supplements
Qualifications
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
Environment
Work Environment & 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 CEO
Compensation
Salary & Benefits
Competitive Salary And Benefits Package Depending On Candidate's Experience.
Culture
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
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.
Apply Now
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.
Responsibilities
Regulatory Strategy and Leadership
The 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 standards
Responsibilities
Business Development and Practice Management
This 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 markets
Responsibilities
Technical and Promotional Compliance
Precision 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 supplements
Qualifications
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
Environment
Work Environment & 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 CEO
Compensation
Salary & Benefits
Competitive Salary And Benefits Package Depending On Candidate's Experience.
Culture
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
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.
Apply Now