Health Care Life Sciences Regulatory Associate — Washington, D.C.

Mid-level associate role in a national health care practice focused on life sciences and product regulatory work. The role sits in the firm's Washington, D.C. office and involves advising biotechnology, life sciences and technology clients on U.S. FDA matters and broader regulatory strategy.

You will support regulatory due diligence and cross-border transactional work, help clients develop compliance approaches across multiple jurisdictions, and monitor and summarize regulatory and legislative developments for clients.

• 3–6 years post-qualification experience at a law firm, government agency, or in-house legal team
• Substantive experience with life sciences product regulatory law and U.S. FDA pathways
• Demonstrated ability to manage complex, client-facing matters in a fast-paced environment
• Strong research, writing, and analytical skills; able to produce clear, actionable advice
• Admission to one or more state bars
• Preferred: experience with cell & gene therapy or advanced biotech regulation, familiarity with reimbursement/CMS frameworks, cross-border regulatory experience, and language skills (e.g., Japanese or Mandarin) where applicable