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Confidential

FDA & Regulatory Compliance Attorney

South Walpole, MA

Check who can apply and the requirements below before continuing.

About this opportunity

Confidential lists this FDA & Regulatory Compliance Attorney opportunity in South Walpole, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.

Job description

Role Overview

Apply FDA and regulatory compliance expertise to help improve next-generation AI systems through accurate, real-world legal analysis. This remote contract role focuses on producing clear, high-quality insights that strengthen how AI models reason about FDA requirements and regulatory risk.

Key Responsibilities

Analyze and interpret FDA statutes, regulations, and guidance documents.

Review and critique regulatory submissions, compliance documentation, and procedural materials.

Assess scenarios for regulatory risk, enforcement trends, and liability considerations.

Draft or edit scenario-based questions and answers that explain regulatory best practices.

Identify emerging FDA and broader regulatory compliance issues and recommend practical solutions.

Explain complex legal requirements clearly in writing and verbally for technical and non-technical audiences.

Provide feedback to improve the accuracy and completeness of project deliverables.

Qualifications

Juris Doctor degree and an active license to practice law in the United States.

At least 5 years of experience in FDA law, regulatory strategy, or compliance within life sciences, pharmaceuticals, or medical devices.

Strong knowledge of federal regulatory processes, submission pathways, and compliance protocols.

Expertise in FDA regulatory analysis, legal research, regulatory compliance, risk assessment, regulatory submissions, and legal writing.

Excellent written and verbal communication skills, including the ability to make complex legal concepts understandable.

Ability to assess ambiguous regulatory developments and translate them into actionable insights.

Strong attention to detail, issue-spotting ability, and commitment to accurate, high-quality work.

Experience advising or representing clients in FDA investigations, warning letters, or consent decrees is preferred.

Work Terms

Remote, independent contractor engagement.

No prior AI experience is required.

Compensation

$140 to $400 per hour.

Application Process

Submit an application by email or through the available application options. Continuing with the application confirms acknowledgment of the candidate terms and privacy policy.

Who can apply

Review the original listing for work authorization, qualifications and employer requirements.

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