Location: Flexible (office located in greater Minneapolis/St. Paul area)
Licensure: Unrestricted license to practice law in a U.S. state
Preferred License: Admission to any federal district court
Level: Mid-level
Exempt Status: Exempt
Hours of Work: Varies
Travel Required: Yes (minimal, e.g., <5%)
Essential Qualifications:
2+ years of experience advising or working within the medical device, pharmaceutical, biologic, or diagnostic industry, either in-house (e.g., Legal, Regulatory Affairs, Compliance) or in a law firm serving FDA-regulated clients.
Experience with U.S. health care compliance laws and regulations (e.g., Food, Drug and Cosmetic Act (FDCA), Anti-Kickback Statute (AKS), False Claims Act (FCA), and Physician Payments Sunshine Act (PPSA)).
Experience with health care anti-fraud compliance matters, e.g., health care compliance auditing and monitoring experience.
Experience with FDA regulatory matters, including advertising and promotion review.
Strong risk assessment and issue-spotting skills; ability to design practical, business-aligned solutions.
Demonstrated ability to advise clients directly and communicate complex concepts clearly and persuasively.
Experience drafting and delivering compliance policies, procedures, and training.
Demonstrates ability to lead projects and teams.
Responsive, persistent, and capable of managing multiple priorities in a fast-paced environment.
Flexible, independent, and self-starting.
Collaborative, business-minded, and professional under pressure.
Exceptional attention to detail.
Excellent written and verbal communication skills.
Juris Doctor (or equivalent) from an ABA-accredited law school.
Licensed and in good standing to practice law in a U.S. state.
Strong grasp of ethics laws and the Model Rules of Professional Conduct.
Gardner Law is an FDA law firm that specializes in regulatory, compliance, privacy, litigation, and commercial matters. Improving health and enhancing lives is our purpose at Gardner Law and it guides everything we do.