Associate, FDA Regulations - DC
$225,000–$435,000 year
On-site · Washington, District of Columbia, United States
Job Summary
FDA Regulatory Associate at a nationally recognized law firm in Washington, DC. Responsibilities include advising clients on FDA regulatory matters with a focus on drug and medical device compliance (CGMP), drafting/reg reviewing regulatory submissions, compliance policies, internal procedures, and contracts; providing guidance during FDA inspections, investigations, and enforcement actions; conducting legal research on FDA laws and enforcement trends; collaborating with clients and internal teams to develop regulatory strategies; staying current on evolving FDA regulations and guidance documents. Ideal candidate has 4–5 years of FDA regulatory compliance experience (law firm or in-house), knowledge of CGMP and FDA frameworks, a scientific background in analytical chemistry/chemical engineering/microbiology, and active DC bar membership or eligibility to waive; excellent research, analytical, and communication skills. Compensation varies by class year, with listed annual salaries from $225,000 to $435,000. Locations include Washington, DC, USA (office-based).
Required Qualifications
- 4–5 years of FDA regulatory compliance experience
- Active bar membership in the District of Columbia, or eligibility to waive in through reciprocity or UBE transfer
- Strong written and verbal communication abilities
- Exceptional research, analytical, and problem-solving skills
- Scientific background in analytical chemistry, chemical engineering, or microbiology (strongly preferred)
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.