Junior to Mid-Level Associate - Medical Device and Technology

BCG Attorney Search; Washington (District of Columbia); On-site; USD 140,000 - 190,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) retirement plan

Job summary

BCG Attorney Search in Washington, DC seeks a junior to mid-level associate for the Medical Devices group within FDA regulatory practice. You will advise on premarket and post-market compliance, enforcement, and strategic regulatory matters in the medical device sector.

The role emphasizes strong writing, analytical skills, and the ability to navigate evolving FDA pathways, with potential to advance as you gain experience in a dynamic legal landscape.

Qualifications

• Demonstrated interest in FDA regulatory law and medical device issues.
• Experience with FDA medical device matters preferred.
• Admission to the District of Columbia Bar.
• Outstanding writing and analytical skills.
• Strong academic credentials and commitment to excellence.

Responsibilities

• Advise clients on FDA regulatory pathways and compliance strategies.
• Support preparation and submission of premarket applications, including 510(k) notifications and PMAs.
• Assist in navigating FDA review processes and responding to agency inquiries.
• Work on post-market compliance, including recalls and adverse event reporting.
• Engage with evolving legal and policy landscapes for AI-enabled medical devices.
• Develop strategies for bringing innovative technologies to market.

Skills

Strong communication

Problem-solving

Analytical skills

Regulatory writing

Education

Law degree from ABA-accredited law school

Job description

Job Overview

A law firm seeks a junior to mid-level associate to join the Medical Devices group within their Food, Drug, Medical Device, and Agriculture practice in Washington, D.C. This role involves advising clients on premarket and post-market compliance, enforcement, and strategic regulatory matters in the medical device sector.

Duties

• Advise clients on FDA regulatory pathways and compliance strategies.
• Support preparation and submission of premarket applications, including 510(k) notifications and PMAs.
• Assist in navigating FDA review processes and responding to agency inquiries.
• Work on post-market compliance, including recalls and adverse event reporting.
• Engage with evolving legal and policy landscapes for AI-enabled medical devices.
• Develop strategies for bringing innovative technologies to market.

Requirements

• Demonstrated interest in FDA regulatory law and medical device issues.
• Experience with FDA medical device matters preferred.
• Admission to the District of Columbia Bar.
• Outstanding writing and analytical skills.
• Strong academic credentials and commitment to excellence.

Education

• Law degree from an ABA-accredited law school.

Certifications

• Admitted to the District of Columbia Bar or eligible to waive in.

Skills

• Strong communication and problem-solving skills.
• Ability to convey complex regulatory concepts clearly.
• Responsive and client-focused with a strong work ethic.

Benefits

• Medical, dental, and vision insurance.
• 401(k) retirement plan.
• Paid time off.
• Potential relocation benefits.